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1
Nie, Ruixue, Xiaotong Zheng, Wenhui Zhang, et al. "Morphological Characteristics and Transcriptome Landscapes of Chicken Follicles during Selective Development." Animals 12, no. 6 (2022): 713. http://dx.doi.org/10.3390/ani12060713.
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Ovarian follicle selection largely depends on the transition of granulosa cells from an undifferentiated to a fully differentiated state, which is accompanied by morphological and functional changes in follicles. The processes and transcriptional regulation of follicles during follicle selection are unclear; we thus used follicles from the prehierarchal to the hierarchal stage to investigate histology, reproductive endocrinology, and transcription. The morphology of follicles changed markedly during follicle selection. The numbers of large white, small yellow, and large yellow follicles (LWF, SYF, and LYF, respectively) were 11.83 ± 2.79, 6.83 ± 2.23, and 1.00, respectively, per ovary. LYF showed thicker granulosa cell layers than those of other prehierarchal follicles. Progesterone concentrations were significantly higher in LYF than that in LWF and SYF. In total, 16,823 genes were positively expressed in LWF, SYF, and LYF. Among follicle types, 1290 differentially expressed genes were enriched regarding cell differentiation, blood vessel morphogenesis, and response to steroid hormones. Candidate genes associated with follicle selection participated in the Wnt signaling pathway, steroid hormone biosynthesis, and the TGF-β signaling pathway. We produced insights into crucial morphological characteristics of transcriptional regulation in follicle development. Our results provide an important basis for revealing the mechanism of follicle selection and potential impact on the poultry industry.
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Kezele, Phillip, and Michael K. Skinner. "Regulation of Ovarian Primordial Follicle Assembly and Development by Estrogen and Progesterone: Endocrine Model of Follicle Assembly." Endocrinology 144, no. 8 (2003): 3329–37. http://dx.doi.org/10.1210/en.2002-0131.
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Abstract The assembly of the developmentally arrested primordial follicle and the subsequent transition of the primordial follicle to the primary follicle are critical processes in normal ovarian physiology that remain to be elucidated. Ovarian follicles do not proliferate and the primordial follicles present in the neonate represent the total number of gametes available to a female throughout her reproductive life. The primordial follicles are oocytes surrounded by less differentiated squamous granulosa cells and are derived from oocyte nests, and primary follicles are oocytes surrounded by a single layer of cuboidal granulosa cells that have initiated follicle development. Abnormalities in primordial follicle assembly, arrest, and development (i.e. primordial to primary follicle transition) can cause pathological conditions such as premature ovarian failure. In this study newborn rat ovaries were cultured for 7 d. The rate of primordial follicle assembly in vivo was identical with the rate in vitro. Interestingly, the rate of primordial follicle transition to the primary follicle was found to be 3 times greater in culture. This abnormal rate of primary follicle development in culture suggests the primordial follicle does not arrest in development as observed in vivo. To investigate this phenomena newborn rat ovaries were cultured in the presence of progesterone, estradiol or calf serum. Estradiol, progesterone, or calf serum significantly reduced the level of initial primordial to primary follicle transition. Approximately 60% of follicles make the primordial to primary follicle transition in control ovaries and about 30% in treated ovaries. Steroids and calf serum had no effect on the primordial to primary follicle transition in ovaries collected and cultured from postnatal 4-d-old rats, suggesting the effects observed are restricted to the initial wave of primordial to primary follicle transition. Interestingly, progesterone was also found to significantly reduce the rate of primordial follicle assembly. All viable oocytes assembled into primordial follicles in control ovaries and approximately 40% remained unassembled in progesterone-treated ovaries. Progesterone was also found to reduce primordial follicle assembly in vivo with 10% of the total follicles remaining unassembled in progesterone injected neonatal animals. Analysis of cellular apoptosis demonstrated that progesterone inhibited the coordinated oocyte apoptosis required for primordial follicle assembly. The hypothesis developed is that high levels of maternal and fetal steroids prevent premature primordial follicle assembly and primordial to primary follicle transition in the embryo. After birth steroid levels fall dramatically and the primordial follicles are free to assemble and initiate development. These observations suggest a novel role for steroids and the maternal-fetal endocrine unit in the control of ovarian primordial follicle assembly and early follicular development.
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Nagashima, Jennifer B., Andrea M. Hill, and Nucharin Songsasen. "In vitro development of mechanically and enzymatically isolated cat ovarian follicles." Reproduction and Fertility 2, no. 1 (2021): 35–46. http://dx.doi.org/10.1530/raf-20-0067.
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Graphical Abstract Isolation of ovarian follicles is a key step in culture systems for large mammalian species to promote the continued growth of follicles beyond the preantral stage in fertility preservation efforts. Still, mechanical isolation methods are user-skill dependent and time-consuming, whereas enzymatic strategies carry increased risk of damaging theca cell layers and the basement membranes. Here, we sought to determine an optimal method to rescue domestic cat (Felis catus) early antral and antral stage follicles from ovarian tissue and to evaluate the influence of isolation strategy on follicle development, survival, and gene expression during 14 days of in vitro culture in alginate hydrogel. Mechanical isolation was compared with 90 min digestion in 0.7 and 1.4 Wünsch units/mL Liberase blendzyme (0.7L and 1.4L, respectively). Mechanical isolation resulted in improved follicle growth and survival, and better antral cavity and theca cell maintenance in vitro, compared with 1.4L (P < 0.05) but displayed higher levels of apoptosis after incubation compared with enzymatically isolated follicles. However, differences in follicle growth and survival were not apparent until 7+ days in vitro. Expressions of CYP19A1, GDF9, LHR, or VEGFA were similar among isolation-strategies. Cultured follicles from all isolation methods displayed reduced STAR expression compared with freshly isolated follicles obtained mechanically or via 0.7L, suggesting that prolonged culture resulted in loss of theca cell presence and/or function. In sum, early antral and antral stage follicle development in vitro is significantly influenced by isolation strategy but not necessarily observable in the absence of extended culture. These results indicate that additional care must be taken in follicle isolation optimizations for genome rescue and fertility preservation efforts. Lay summary The ovary contains hundreds of eggs with only a select few developing from an immature stage through to ovulation over the course of an animal's lifetime. Rescue of eggs from this pool, and the ability to grow them in culture to a mature stage, would be incredibly valuable for fertility preservation efforts in both humans and endangered species. Currently, the isolation of ovarian follicles (eggs with their surrounding helper cells) is a key step in culture systems for large mammalian species, to promote continued growth. Yet, isolation methods may affect the follicle’s future developmental capacity. We evaluated two isolation strategies, mechanical micro-dissection (needle/scalpel blade) and enzymatic digestion (using Liberase blendzyme) on ovaries of domestic cats obtained via routine spay procedures. Mechanically isolated follicles displayed improved growth, survival, and indications of developmental competence in 14-day culture, compared with high concentration (1.4 Wünsch units/mL) enzyme-isolated follicles. However, mechanical isolation was not different from low (0.7 Wünsch units/mL) enzyme for these metrics, or for expression of key genes indicative of follicular cell functions. Further, differences in follicle growth/survival were not apparent until 7+ days in culture. Thus, ovarian follicle isolation strategies influence developmental potential in culture, and extended culture will be required to identify optimal methods for fertility preservation efforts.
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Durlinger, Alexandra L. L., Maria J. G. Gruijters, Piet Kramer, et al. "Anti-Müllerian Hormone Attenuates the Effects of FSH on Follicle Development in the Mouse Ovary." Endocrinology 142, no. 11 (2001): 4891–99. http://dx.doi.org/10.1210/endo.142.11.8486.
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Abstract Although ovarian follicle growth is under the influence of many growth factors and hormones of which FSH remains one of the most prominent regulators. Therefore, factors affecting the sensitivity of ovarian follicles to FSH are also important for follicle growth. The aim of the present study was to investigate whether anti-Müllerian hormone (AMH) has an inhibitory effect on follicle growth by decreasing the sensitivity of ovarian follicles to FSH. Furthermore, the combined action of AMH and FSH on ovarian follicle development was examined. Three different experiments were performed. Using an in vitro follicle culture system it was shown that FSH-stimulated preantral follicle growth is attenuated in the presence of AMH. This observation was confirmed by an in vivo experiment showing that in immature AMH-deficient females, more follicles start to grow under the influence of exogenous FSH than in their wild-type littermates. In a third experiment, examination of the follicle population of 4-month-old wild-type, FSHβ-, AMH-, and AMH-/FSHβ-deficient females revealed that loss of FSH expression has no impact on the number of primordial and preantral follicles, but the loss of inhibitory action of AMH on the recruitment of primordial follicles in AMH-deficient mice is increased in the absence of FSH. In conclusion, these studies show that AMH inhibits FSH-stimulated follicle growth in the mouse, suggesting that AMH is one of the factors determining the sensitivity of ovarian follicles for FSH and that AMH is a dominant regulator of early follicle growth.
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Moore, GPM, N. Jackson, K. Isaacs, and G. Brown. "Development and density of wool follicles in Merino sheep selected for single fibre characteristics." Australian Journal of Agricultural Research 47, no. 8 (1996): 1195. http://dx.doi.org/10.1071/ar9961195.
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Wool follicles are classified into 3 major types: primary (P), original secondary (SO), and derived secondary (SD). They are formed during fetal life as successive waves of initiation pass through the skin. P follicles are the first to be initiated. SO follicles develop between the primaries and are separated from them at non-randomly distributed sites. SD follicles are the last to be initiated and branch from SO and other SD follicles. We have measured the densities of these follicles in 4 lines of sheep selected for different fleece characters. Primary follicle and total follicle densities (NP and NP + NS) were estimated by conventional procedures. The densities of pilary canals were also obtained to provide a measure of Np + NSO. Follicle counts in both adult and fetal animals showed that NP and NP + NSO were relatively constant across the lines. Predominantly, density differences were due to variations in the numbers of follicles initiated during the last wave, forming the derived secondary population. Changes in follicle densities were therefore effected by developmental mechanisms that increase or decrease the extent of branching rather than by altering the numbers of P and SO follicles. The results suggest firstly that the numbers of initiation sites for P or SO follicle formation in the fetus, corresponding to the pilary canals of adult skin, are limited. Secondly, the skin has the capacity to continue to initiate follicles after most or all of the sites have been occupied. It is concluded that the mechanisms controlling follicle initiation site densities and total follicle densities are independently regulated in the sheep. The observations are discussed in relation to factors that influence the densities of the different follicle types. The results have practical implications for changing fleece weight and fibre diameter through selective breeding.
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Cossigny (Rosairo), D. A., J. K. Findlay, and A. E. Drummond. "123. ACTIVIN A AND OVARIAN FOLLICLE DEVELOPMENT." Reproduction, Fertility and Development 21, no. 9 (2009): 42. http://dx.doi.org/10.1071/srb09abs123.
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A significant developmental stage in ovarian folliculogenesis is the acquisition of gonadotropin sensitivity by ovarian follicles. Activin has previously been suggested to be involved in the responsiveness of granulosa cells to FSH (1). Therefore, the role of activin was investigated using a ‘physiological’ culture system to determine if pathways exist to transduce activin signals within the postnatal rat ovary. Organ cultures with day 4 whole ovaries were employed in order to assess the potential impact of Activin A on follicle growth and transition from the primordial through to the primary and later preantral stages of development. Ovaries were isolated and cultured for 10 days with the addition of supplemented DMEM/Hams F-12 media (2)and either FSH (100ng/ml), Activin A (50ng/ml), or a combination of the two. Media and treatments were refreshed every alternate day. At the end of the culture period, ovaries were fixed and sectioned, or placed immediately into Ultraspec for RNA extraction for future real-time PCR. Sections were used for morphological assessment and ovarian follicle counting of primordial, primary and preantral follicles. An evaluation of atresia by the detection of apoptotic cells was undertaken using terminal deoxynucleotidyl transferase (TdT) mediated dUTP-biotin nick-end labeling (TUNEL). Primary follicle numbers increased significantly (P<0.05) in the combined treatment group whereas, preantral follicle numbers increased significantly (P<0.0001) when treated with Activin A alone. This is consistent with a morphological appraisal of atresia where a decrease in atresia was found in primordial and primary follicles, supporting the primary follicle development data and Activin A treatment alone resulted in more healthy primary and preantral follicles than atretic ones. Therefore, a stimulatory role for Activin A both in the presence of FSH (primary follicle development) or alone (preantral follicle development) has resulted in more follicles making the transition from the primordial to primary stages, as well as to the later preantral stages.
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McGee, Elizabeth A., and Aaron J. W. Hsueh. "Initial and Cyclic Recruitment of Ovarian Follicles*." Endocrine Reviews 21, no. 2 (2000): 200–214. http://dx.doi.org/10.1210/edrv.21.2.0394.
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Abstract Mammalian ovaries consist of follicles as basic functional units. The total number of ovarian follicles is determined early in life, and the depletion of this pool leads to reproductive senescence. Each follicle develops to either ovulate or, more likely, to undergo degeneration. The dynamics of ovarian follicle development have interested endocrinologists and developmental biologists for many years. With the advent of assisted reproductive techniques in humans, the possibility of regulating follicle development in vivo and in vitro has gained clinical relevance. In this review, we focus upon key branching points during the development of ovarian follicles as well as factors involved in determining the eventual destiny of individual follicles. We discuss inconsistencies in the literature regarding the definitions of follicle recruitment and selection and propose to name the two major steps of follicle development as initial and cyclic recruitment, respectively. Because some of these disparities have arisen due to differences in the animal systems studied, we also compare the development of the ovarian follicles of both humans and rats. We also review the status of knowledge of several puzzling clinical issues that may provide important clues toward unlocking the mechanisms of follicle development.
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Schauer, S. N., S. D. Sontakke, E. D. Watson, C. L. Esteves, and F. X. Donadeu. "Involvement of miRNAs in equine follicle development." REPRODUCTION 146, no. 3 (2013): 273–82. http://dx.doi.org/10.1530/rep-13-0107.
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Previous evidence fromin vitrostudies suggests specific roles for a subset of miRNAs, including miR-21, miR-23a, miR-145, miR-503, miR-224, miR-383, miR-378, miR-132, and miR-212, in regulating ovarian follicle development. The objective of this study was to determine changes in the levels of these miRNAs in relation to follicle selection, maturation, and ovulation in the monovular equine ovary. In Experiment 1, follicular fluid was aspirated during ovulatory cycles from the dominant (DO) and largest subordinate (S) follicles of an ovulatory wave and the dominant (DA) follicle of a mid-cycle anovulatory wave (n=6 mares). Follicular fluid levels of progesterone and estradiol were lower (P<0.01) in S follicles than in DO follicles, whereas mean levels of IGF1 were lower (P<0.01) in S and DA follicles than in DO follicles. Relative to DO and DA follicles, S follicles had higher (P≤0.01) follicular fluid levels of miR-145 and miR-378. In Experiment 2, follicular fluid and granulosa cells were aspirated from dominant follicles before (DO) and 24 h after (L) administration of an ovulatory dose of hCG (n=5 mares/group). Relative to DO follicles, L follicles had higher follicular fluid levels of progesterone (P=0.05) and lower granulosa cell levels ofCYP19A1andLHCGR(P<0.005). Levels of miR-21, miR-132, miR-212, and miR-224 were increased (P<0.05) in L follicles; this was associated with reduced expression of the putative miRNA targets,PTEN,RASA1, andSMAD4. These novel results may indicate a physiological involvement of miR-21, miR-145, miR-224, miR-378, miR-132, and miR-212 in the regulation of cell survival, steroidogenesis, and differentiation during follicle selection and ovulation in the monovular ovary.
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Feeney, Amanda, Eric Nilsson, and Michael K. Skinner. "Cytokine (IL16) and tyrphostin actions on ovarian primordial follicle development." REPRODUCTION 148, no. 3 (2014): 321–31. http://dx.doi.org/10.1530/rep-14-0246.
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An ovarian follicle is composed of an oocyte and surrounding theca and granulosa cells. Oocytes are stored in an arrested state within primordial follicles until they are signaled to re-initiate development by undergoing primordial-to-primary follicle transition. Previous gene bionetwork analyses of primordial follicle development identified a number of critical cytokine signaling pathways and genes potentially involved in the process. In the current study, candidate regulatory genes and pathways from the gene network analyses were tested for their effects on the formation of primordial follicles (follicle assembly) and on primordial follicle transition using whole ovary organ culture experiments. Observations indicate that the tyrphostin inhibitor (E)-2-benzylidene-3-(cyclohexylamino)-2,3-dihydro-1H-inden-1-one increased follicle assembly significantly, supporting a role for the MAPK signaling pathway in follicle assembly. The cytokine interleukin 16 (IL16) promotes primordial-to-primary follicle transition as compared with the controls, where as Delta-like ligand 4 (DLL4) and WNT-3A treatments have no effect. Immunohistochemical experiments demonstrated the localization of both the cytokine IL16 and its receptor CD4 in the granulosa cells surrounding each oocyte within the ovarian follicle. The tyrphostin LDN193189 (LDN) is an inhibitor of the bone morphogenic protein receptor 1 within the TGFB signaling pathway and was found to promote the primordial-to-primary follicle transition. Observations support the importance of cytokines (i.e., IL16) and cytokine signaling pathways in the regulation of early follicle development. Insights into regulatory factors affecting early primordial follicle development are provided that may associate with ovarian disease and translate to improved therapy in the future.
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Ruoss, Chantelle, Amanda Tadros, Tim O'Shea, Jim McFarlane, and Ghanim Almahbobi. "Ovarian follicle development in Booroola sheep exhibiting impaired bone morphogenetic protein signalling pathway." REPRODUCTION 138, no. 4 (2009): 689–96. http://dx.doi.org/10.1530/rep-09-0190.
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The role of bone morphogenetic proteins (BMPs) in the regulation of ovarian function has been extensively investigated but the mechanism of regulation is not well understood. The aim of this study was to investigate the effect of mutation in the BMP receptor in Booroola sheep on the number of primordial follicles and rate of follicle recruitment in comparison with that in normal merino sheep in vivo. Whole sheep ovaries at the time of birth, 1.5 and 5 years old were collected and processed for the follicle quantification, using computerised stereological methods and statistical analyses. At birth, the total number of primordial follicles in Booroola sheep was significantly lower than in merino sheep. At 1.5 and 5 years, a reversed pattern in favour of Booroola ewes was seen with significantly more primordial follicles than merino. In parallel, the rate of primordial follicle recruitment to developing cohort was substantially lower in Booroola ewes with only 51 and 66% of primordial follicle consumption at 1.5 and 5 years respectively compared to 92 and 97% in merino ewes. On other hand, the mean numbers of developing primary follicles were smaller in Booroola sheep at the time of birth, yet, Booroola ewes possess more primary follicles than merino at 1.5 years. These findings suggest that attenuation of the intraovarian signalling pathway of BMPs may in fact be a successful means of rationalising follicle consumption, preventing unnecessary loss of follicles from the initial primordial follicle pool, hence increasing reproductive longevity and fertility.
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Thomas, Fiona H., Bruce K. Campbell, David G. Armstrong, and Evelyn E. Telfer. "Effects of IGF-I bioavailability on bovine preantral follicular development in vitro." Reproduction 133, no. 6 (2007): 1121–28. http://dx.doi.org/10.1530/rep-06-0382.
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The aim of this study was to determine the effect of regulation of IGF-I bioavailability on preantral follicle development in vitro. Bovine preantral follicles were cultured for 6 days in serum-free medium with increasing doses of Long R3 (LR3) IGF-I (an analog with low affinity for IGF-binding proteins (IGFBPs)), or human recombinant IGF-I (hrIGF-I). Follicle diameter and estradiol production were measured every second day. On day 6, ratios of oocyte/follicle diameter and oocyte morphology were assessed by histological examination, and IGFBP-2 and -3 were detected by immunocytochemistry and in situ hybridization respectively. Both types of IGF-I increased follicle diameter in a dose-dependent manner (P < 0.05) and increased estradiol production over control levels (P < 0.05). However, follicles treated with LR3 IGF-I and the highest concentration of hrIGF-I (1000 ng/ml) had smaller oocyte/follicle ratios, and increased oocyte degeneration, compared with controls or follicles treated with physiological concentrations of hrIGF-I (P < 0.05). IGFBPs were detected in cultured preantral follicles, indicating a requirement for regulation of IGF bioavailability during the early stages of follicular development. Specifically, IGFBP-3 mRNA was found to be expressed in oocytes, and IGFBP-2 immunoreactivity was detected in oocytes and granulosa cells of cultured follicles. In summary, the regulation of IGF-I bioavailability by IGFBPs is necessary for the co-ordination of oocyte and follicle development in vitro.
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Ryan, K. E., S. M. Casey, M. J. Canty, M. A. Crowe, F. Martin, and A. C. O. Evans. "Akt and Erk signal transduction pathways are early markers of differentiation in dominant and subordinate ovarian follicles in cattle." Reproduction 133, no. 3 (2007): 617–26. http://dx.doi.org/10.1530/rep-06-0130.
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Dominant follicles are those that continue to develop and have the potential to ovulate while subordinate follicles regress. Characteristics of dominant follicles include a larger diameter, higher intrafollicular estradiol, and lower IGF-binding protein (IGFBP)-4 concentrations compared with other cohort follicles. Follicle development is regulated by endocrine hormones that act via intracellular signaling pathways. Here, we show the differences in Akt, Erk, c-Jun N-terminal protein kinase, and p-38 signaling pathways between dominant and subordinate follicles at the dominance stage of the follicle wave. However, earlier in the follicle wave (dominant follicle selection), there were only differences in the levels of Akt and Erk signal transduction proteins among dominant and subordinate follicles. Using this profile of Akt and Erk protein expression in granulosa and theca cells of selected dominant follicles compared with subordinate follicles, we suggest a predictive model to identify future dominant and subordinate follicles from the pool of otherwise similar cohort follicles at the time of follicle wave emergence. We conclude that the Erk and Akt signal transduction pathways are important for dominant follicle selection and development and, furthermore, that the observed differences in these pathways mark the future dominant follicle from subordinate follicles before differences in follicular diameter, follicular fluid estradiol, and IGFBP-4 concentrations are apparent.
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Diao, Xiaogao, Lingyun Yao, Xinhui Wang, et al. "Hair Follicle Development and Cashmere Traits in Albas Goat Kids." Animals 13, no. 4 (2023): 617. http://dx.doi.org/10.3390/ani13040617.
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The objectives of this trial were to study the growth and development of hair follicles and cashmere traits in cashmere goats and to provide a theoretical basis for the regulation of secondary hair follicle development and the scientific breeding selection of cashmere goats. Twelve single-fetal female kids were selected as research objects. A long-term tracking plan was created to regularly determine their growth performance, cashmere performance, and hair follicle traits. The results showed no significant difference in live weight after the first and second combing. The cashmere yield and unit yield of the first combing were significantly higher than those of the second combing (p < 0.05). Sections of hair follicles showed that the primary hair follicles are almost fully developed by 1 month, and the secondary hair follicles are fully developed by 5–6 months after birth. The primary hair follicle density (PFD) and secondary hair follicle density (SFD) were highest at birth and decreased within 1 month; and SFD was stable at 5–6 months of age. The change of MSFD took a maximum time of 2 to 3 months. The S:P increase reached its peak at 6 months. BMP4 expression increased with time. FGF2, FGF21 and BMP7 were higher at 3 months old than at the other two-time points. In conclusion, this study determined the total development time of primary and secondary hair follicles from morphology and speculated that FGF2, FGF21, and BMP7 may play a regulatory role in developing secondary hair follicles. Therefore, the period from birth to 6 months of age was the best time to regulate secondary hair follicle development in cashmere goats kids. The traits of the hair follicle and cashmere at 6 months of age could be breeding selection indicators for cashmere goats.
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Nagorcka, BN. "The reaction-diffusion (RD) theory of wool (hair) follicle initiation and development. II. Original secondary follicles." Australian Journal of Agricultural Research 46, no. 2 (1995): 357. http://dx.doi.org/10.1071/ar9950357.
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In an accompanying paper it was shown that a spatial prepattern mechanism based on a biochemical reaction referred to as a reaction-diffusion (RD) system is able to account for many aspects of the initiation and development of primary (P) wool follicles. In this paper the same RD system is applied to the initiation and development of original secondary (SO) follicles. Prepatterns are generated by solving the equations describing the reaction and diffusion of the chemical components of the RD system in early stage follicles. It is demonstrated that the prepattern mechanism can account for the loss of a sweat gland causing a change from P follicle initiation to SO follicle initiation. The RD system equations are also solved in the epidermis. The time sequence of prepatterns obtained in the epidermis account for the tendency of SO follicles to group with P follicles, by initiating in-between members of the trio group of P follicles as well as in between existing SO follicles. The prepatterns obtained did not account for the tendency of secondary follicles to initiate on the posterior side of the trio group. Good agreement was obtained between the predicted increase in total follicle density and the increase in follicle density observed during follicle initiation by Carter and Hardy (1947), provided full account was taken of the interaction between existing follicles and each new future generations of follicles. The prepattern mechanism provides a fundamental basis for an inverse genetic correlation between total P and SO follicle density and fibre diameter.
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Binelli, Mario, and Bruce D. Murphy. "Coordinated regulation of follicle development by germ and somatic cells." Reproduction, Fertility and Development 22, no. 1 (2010): 1. http://dx.doi.org/10.1071/rd09218.
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The continuum of folliculogenesis begins in the fetal ovary with the differentiation of the oogonia and their isolation within the primordial follicles. Primordial follicle activation is an enigmatic process, whereby some follicles enter the growing pool to become primary follicles, thereby embarking on an irreversible progression towards ovulation or atresia. This process is under the coordinated regulation of factors from the oocyte itself, as well as from the somatic cells of the ovary, in particular the theca and granulosa cells, which are structural components of the follicle. These two influences provide the principal stimuli for the growth of the follicle to the late preantral or early antral stage of development. The endocrine effects of the gonadotrophins FSH and LH are essential to the continued progression of the follicle and most atresia can be attributed to the failure to receive or process the gonadotrophin signals. The peri-ovulatory state has received intensive investigation recently, demonstrating a coordinated role for gonadotrophins, steroids, epidermal growth factor family proteins and prostaglandins. Thus, a complex programme of coordinated interaction of governing elements from both germ and somatic cell sources is required for successful follicle development.
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Vlaisavljevic, Veljko. "Echographic Evidence of Follicle Development and Maturation." Donald School Journal of Ultrasound in Obstetrics and Gynecology 5, no. 3 (2011): 267–72. http://dx.doi.org/10.5005/jp-journals-10009-1203.
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ABSTRACT Monitoring of individual follicles during the menstrual cycle demonstrates in a non-invasive way the changes in their number and position during the early and the late follicular phase and the luteal phase. The differences in relations between the follicles near the dominant follicle can be demonstrated with the same technique using 3D reconstruction of the ovary. Recognition of the follicle growth pattern has a prognostic value for the outcome of assisted reproduction methods. Follicular diameter and changes in growth patterns are more important than follicular wall thickness as parameters having an impact on clinical success. An increased perifollicular blood flow can be measured in the perifollicular period using color and pulsed Doppler. Automated estimation of blood volume around the ovarian follicles brought a new concept to this area. Results confirm the observation that vascularity around the follicle is intense in the periovulatory period. From our results we can hypothesize that those follicles containing oocytes able to produce pregnancy have a prominent and more uniform perifollicular vascular network .
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Laura Maria Andrade Silva, Ricardo Hsieh, Silvia Vanessa Lourenço, Verônica Ottoni, Neusa Valente, and Juliana Dumet Fernandes. "Immunoexpression of Adhesion Molecules During Human Fetal Hair Development." Revista Científica Hospital Santa Izabel 5, no. 3 (2021): 159–66. http://dx.doi.org/10.35753/rchsi.v5i3.222.
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SummaryBackground: Hair follicles are produced in a cyclical manner and the machinery involved in the reproduction of these follicles is present since the fetal stage. Although extensive research has been done on the human hair follicle, very little is known about the importance of adhesion molecules in its development. Methods: We analyzed here, the immunoexpression of beta-1 integrin, p-cadherin, e- cadherin, and beta-catenin in hair follicles from 26 formalin-fixed and paraffin-embedded skin samples from human embryos and fetus between 12-23 weeks of gestational age. Findings: The adhesion molecules beta-1 integrin and e-cadherin/p-cadherin were expressed from 12 weeks and seemed to play a role in regulating epidermis invagination. Beta-catenin immuno stainingwas negative in all cases; down regulation of this protein may be necessary for fetal hair development and thus facilitating hair follicle down growth. Conclusion: Adhesion molecules are essential for hair follicle down growth and proliferation; integrins and cadherins play a major role in this process. More studies are needed to describe hair follicle development.
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Britt, K. L., P. K. Saunders, S. J. McPherson, M. L. Misso, E. R. Simpson, and J. K. Findlay. "202.Estrogen actions on follicle formation and early follicle development." Reproduction, Fertility and Development 16, no. 9 (2004): 202. http://dx.doi.org/10.1071/srb04abs202.
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Estradiol 17 beta (E2) effects late follicular development whilst primordial follicle formation and early activation are thought to be independent of E2. To test this hypothesis we compared numbers of primordial and primary follicles in wildtype and E2 deficient ArKO mice, and the immunohistochemical staining or mRNA expression of Mullerian inhibiting substance (MIS), Wilms tumour 1 (WT-1), and growth differentiation factor (GDF9), known to effect early follicular differentiation. Proliferating cell nuclear antigen (PCNA) staining was a marker of proliferative index. The effects of E2 replacement for 3 wk in 7 wk old ArKO and wildtype mice on these parameters were also tested. We used unbiased, assumption-free stereological methods for quantification of early follicular numbers in the mouse ovary (1). ArKO mice had reduced numbers of primordial and primary follicles compared to wildtype (63%, p<0.001 and 60%, p=0.062 of Wt respectively). This reduction was not corrected by E2 treatment, suggesting that E2 effects the initial formation or activation of primordial follicles. There was a significant increase in the diameters of the oocytes in primordial follicles of ArKO mice compared to wildtype. There were no differences in the immunostaining of MIS, WT-1 and PCNA in primordial and primary follicles between wildtype and ArKO mice. The only difference was as a consequence of Sertoli and Leydig cells in ovaries of ArKO mice. GDF9 mRNA expression was markedly increased in ArKO ovaries. E2 treatment restored the ovarian follicular morphology, and consequently the immunostaining patterns, but had no effect on early follicle numbers. In conclusion, E2 has a role in controlling the size of the oocyte and primordial follicle pools in mice. Supported by NH&MRC RegKey #241000 and 198705. (1) Britt and Myers (2004) Reproduction 127,:569–580.
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Commin, L., S. Buff, E. Rosset, et al. "Follicle development in cryopreserved bitch ovarian tissue grafted to immunodeficient mouse." Reproduction, Fertility and Development 24, no. 3 (2012): 461. http://dx.doi.org/10.1071/rd11166.
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The present study evaluated: (1) in vivo follicular development in canine ovarian tissue after slow freezing and xenotransplantation; and (2) the use of erythropoietin (EPO) as an angiogenic factor to optimise the transplantation procedure. Frozen–thawed ovarian tissue from five bitches was grafted into severe combined immunodeficient (SCID) mice (n = 47) treated with or without EPO (500 IU kg–1, once daily for 3 days) (Groups A and B, respectively) and analysed after 0, 1, 8 or 16 weeks. Follicle grade, follicle density, follicle morphology and stromal cells density were assessed by histological analysis, whereas vascularisation of the graft was quantified by immunohistochemistry with anti-α-smooth muscle actin antibody. Despite a massive loss of follicles after grafting, secondary follicle density was higher at 8 and 16 weeks than at 1 week regardless of EPO treatment. EPO significantly improved early follicle morphology and stromal cell density after 8 weeks and blood vessel density at 16 weeks after transplantation (P < 0.05). Intact secondary follicles with more than three granulosa cells layers were observed 16 weeks after transplantation. The results suggest that canine ovarian tissue can be successfully preserved by our slow-freezing protocol because the tissue showed follicular growth after xenotransplantation. EPO treatment did not lessen the massive loss of follicles after transplantation.
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Rosairo, D. A., J. K. Findlay та A. E. Drummond. "270. TGF-β and ovarian follicle development". Reproduction, Fertility and Development 20, № 9 (2008): 70. http://dx.doi.org/10.1071/srb08abs270.
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The role TGF-β plays in ovarian follicular growth and differentiation was investigated using a ‘physiological' culture system. TGF- β ligand and receptors are present in the rat ovary from 4 days after birth. Therefore we established organ cultures with these ovaries in order to assess the potential impact of TGF- β1 on follicle growth and transition from the primordial through to the primary and preantral stages of development. Whole ovaries were isolated and cultured for 10 days on floating filters with the addition of supplemented DMEM/Hams F-12 media and either FSH (100ng/mL), TGF- β1 (10ng/mL), or a combination of the two. Media as well as treatments were refreshed every second day. At the end of the culture period, ovaries were fixed in 10% formalin, embedded in paraffin and sectioned at 5µm. Sections were used for morphological assessment and ovarian follicle counting with three serial sections mounted/slide and every alternate slide used for counting of primordial, primary and preantral follicles. An evaluation of atresia by the detection of apoptotic cells was undertaken using terminal deoxynucleotidyl transferase (TdT) mediated dUTP-biotin nick-end labelling (TUNEL) via the ApopTag® Peroxidase in situ apoptosis detection kit. Results gathered from this study show preantral follicle numbers declined significantly when treated with the combination of FSH and TGF- β1, consistent with our morphological appraisal of atresia where the combined treatment appeared to produce more apoptotic follicles than healthy follicles, suggesting an increase in atretic primary and preantral follicles. These preliminary findings suggest an inhibitory role for TGF- β1 in the presence of FSH, resulting in fewer follicles making the transition from the primary to the preantral stage. Further studies are required to test the effects of other TGF-β superfamily members on follicle transition in vitro. Supported by the NHMRC of Australia (Regkeys 241000, 441101, 465415, 198705)
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Nilsson, Eric E., Chris Detzel, and Michael K. Skinner. "Platelet-derived growth factor modulates the primordial to primary follicle transition." Reproduction 131, no. 6 (2006): 1007–15. http://dx.doi.org/10.1530/rep.1.00978.
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Primordial follicles steadily leave the arrested pool and undergo a primordial to primary follicle transition during the female reproductive lifespan. When the available pool of primordial follicles is depleted reproduction ceases and humans enter menopause. The present study was designed to investigate the actions of several growth factors previously identified as candidate regulatory factors for the primordial to primary follicle transition with a microarray analysis. Ovaries from 4-day-old rats were placed into culture and treated for 2 weeks with platelet-derived growth factor (PDGF), anti-PDGF neutralizing antibody, vascular endothelial growth factor (VEGF), neuregulin (NRG), or kit ligand (KITL) as a positive control. PDGF-treatment resulted in a significant decrease in the percentage of primordial follicles and a concomitant increase in the percentage of developing primary follicles compared to controls. In contrast, ovaries treated with an anti-PDGF neutralizing antibody had a significant increase in the percentage of primordial follicles demonstrating an inhibition of endogenous follicle development. Ovaries incubated in the presence of VEGF or NRG had no change in follicle development. Observations indicate that PDGF, but not VEGF or NRG, promotes the primordial to primary follicle transition. Immunohistochemical localization indicated that the PDGF protein was present in the oocytes of both primordial and developing follicles. PDGF-treatment of cultured ovaries resulted in an increase in KITL mRNA expression. KITL has been previously shown to promote the primordial to primary follicle transition. KITL-treatment of ovaries had no effect on expression of Pdgf or any PDGF homologs or receptors. Therefore, PDGF appears to be produced by the oocyte and acts as one of several extracellular signaling factors that regulate the primordial to primary follicle transition. These observations provide insight into the cell–cell interactions involved in the regulation of primordial follicle development and can be used in the future development of therapies for some forms of infertility.
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Dole, Gretchen, Eric E. Nilsson, and Michael K. Skinner. "Glial-derived neurotrophic factor promotes ovarian primordial follicle development and cell–cell interactions during folliculogenesis." REPRODUCTION 135, no. 5 (2008): 671–82. http://dx.doi.org/10.1530/rep-07-0405.
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Female fertility is determined in part by the size and development of the primordial follicle pool. The current study investigates the role of glial cell-line-derived neurotrophic factor (GDNF) in the regulation of primordial follicle development in the ovary. Ovaries from 4-day-old female rat pups were maintained in organ culture for 10 days in the absence (control) or presence of GDNF or kit ligand (KL)/stem cell factor. Ovaries treated with GDNF contained a significant increase in developing follicles, similar to that observed with KL treatment previously shown to promote follicle development. The actions of GDNF on the ovarian transcriptome were investigated with a microarray analysis. Immunohistochemical studies demonstrated that GDNF is localized to oocyte cytoplasm in follicles of all developmental stages, as well as to cumulus granulosa cells and theca cells in antral follicles. GDNF receptor α1 (GFRα1) staining was localized to oocyte cytoplasm of primordial and primary follicles, and at reduced levels in the oocytes of antral follicles. GFRα1 was present in mural granulosa cells of antral follicles, theca cells, and ovarian surface epithelium. The localization studies were confirmed with molecular analysis. Microarray analysis was used to identify changes in the ovarian transcriptome and further elucidate the signaling network regulating early follicle development. Observations indicate that GDNF promotes primordial follicle development and mediates autocrine and paracrine cell–cell interactions required during folliculogenesis. In contrast to the testis, ovarian GDNF is predominantly produced by germ cells (oocytes) rather than somatic cells.
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Annes, Kelly, Diego B. Müller, Jorge A. P. Vilela, et al. "Influence of follicle size on bovine oocyte lipid composition, follicular metabolic and stress markers, embryo development and blastocyst lipid content." Reproduction, Fertility and Development 31, no. 3 (2019): 462. http://dx.doi.org/10.1071/rd18109.
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This study assessed the lipid composition of oocytes from different follicle sizes and compared the expression of lipid-related genes and follicular fluid (FF) molecules between groups. We also investigated the functional consequences of differences on embryo development and blastocyst lipid deposits. Oocytes and FF were recovered from different follicle sizes. Oocytes from small (≤5mm) and large (≥6mm) bovine follicles were used to produce Day 7 expanded blastocysts (Day7Ex) and blastocysts that only became expanded at Day 8 (Day8Ex) after insemination. Oocytes from &gt;8mm follicles had the highest lipid content. Few oocyte phospholipid variations were identified between groups. Very long chain fatty acid elongase 6 (ELOVL6) mRNA abundance was reduced in larger follicle-derived oocytes compared with the ≤2mm group. Increased levels of glucose, reactive oxygen species, glutathione and superoxide dismutase activity were also identified in FF from larger follicles. Large follicle-derived embryo development and lipid content of Day7Ex were greater than those derived from small follicles. Day8Ex had greater lipid deposition than Day7Ex. Oocytes and blastocysts exhibited follicle size-specific lipids. Large-follicle oocytes had increased lipid content and became Day7Ex with greater lipid deposition whereas delayed blastocoel expansion associated with a prolonged period of culture determined the lipid accumulation of Day8Ex. The FF microenvironment of large follicles seems to favour embryo development.
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Zielak, Anna E., Niamh Forde, Stephan D. E. Park, et al. "Identification of novel genes associated with dominant follicle development in cattle." Reproduction, Fertility and Development 19, no. 8 (2007): 967. http://dx.doi.org/10.1071/rd07102.
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Follicle development is regulated by the interaction of endocrine and intrafollicular factors, as well as by numerous intracellular pathways, which involves the transcription of new genes, although not all are known. The aim of the present study was to determine the expression of a set of unknown genes identified by bovine cDNA microarray analysis in theca and granulosa cells of dominant and subordinate follicles, collected at a single stage of the first follicular wave using quantitative real-time polymerase chain reaction. Differences were further examined at three stages of the follicular wave (emergence, selection and dominance) and bioinformatics tools were used to identify these originally unknown sequences. The suggested name function and proposed role for the novel genes identified are as follows: MRPL41 and VDAC2, involved in apoptosis (dominant follicle development); TBC1D1 stimulates cell differentiation (growth associated with dominant follicle selection and development); STX7, promotes phagocytosis of cells (subordinate follicle regression); and SPC22 and EHD3, intracellular signalling (subordinate follicle regression). In conclusion, we have identified six novel genes that have not been described previously in ovarian follicles that are dynamically regulated during dominant follicle development and presumably help mediate intracellular signalling, cell differentiation, apoptosis and phagocytosis, events critical to follicular development.
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McCloghry, CE, DE Hollis, A. Foldes, et al. "The effects of exogenous melatonin and prolactin on wool follicle development in ovine foetal skin grafts." Australian Journal of Agricultural Research 44, no. 5 (1993): 993. http://dx.doi.org/10.1071/ar9930993.
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The fleece of the Merino sheep is composed predominantly of wool fibres grown from secondary wool follicles. This study investigates the effects of melatonin and prolactin on the development of secondarv follicles in grafted ovine foetal skin. Skin from day 85 ovine foetuses was grafted onto nude mice, developed for 40 days and then excised. Mice received either 30 8g prolactin ip mouse-1 day-1 (P), one melatonin implant (Regulin�) sc mouse -1 (M), commencing at grafting or no further treatment (C). Wool follicle density and development were assessed in grafted skin and compared with day 125 control foetal skin. Cuticle structure of graft fibres was also examined and compared with those of day 125 foetuses. Total follicle density and the rate of follicle initiation were reduced in the grafts compared with control foetal skin. Total follicle density did not vary significantly between treatments, but the number of derived secondary follicles was greater in grafts from mice receiving prolactin (group P). Follicles in grafted skin were larger, produced medullated fibres, and were not grouped, in comparison with follicles in the control foetal skin. Epidermal thickness was greater in grafts than in control foetal skin. The cuticle structure of graft fibres from all groups was similar to the control wool fibres. These findings indicate that prolactin, but not melatonin, may be involved in the regulation of derived secondary follicle development.
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Lu, C. L., J. Yan, X. Zhi, et al. "Basic fibroblast growth factor promotes macaque follicle development in vitro." REPRODUCTION 149, no. 5 (2015): 425–33. http://dx.doi.org/10.1530/rep-14-0557.
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Fertility preservation is an important type of frontier scientific research in the field of reproductive health. The culture of ovarian cortices to i) initiate primordial follicle growth and ii) procure developing follicles for later oocyte maturation is a promising fertility preservation strategy, especially for older women or cancer patients. At present, this goal remains largely unsubstantiated in primates because of the difficulty in attaining relatively large follicles via ovarian cortex culture. To overcome this hurdle, we cultured macaque monkey ovarian cortices with FSH, kit ligand (KL), basic fibroblast growth factor (bFGF), and/or epidermal growth factor (EGF). The various factors and factor combinations promoted primordial follicle development to different extents. Notably, both bFF (bFGF, 100 ng/ml and FSH, 50 ng/ml) and KF (KL, 100 ng/ml and FSH, 50 ng/ml) contributed to the activation of primordial follicles at day 12 (D12) of culture, whereas at D18, the proportions of developing follicles were significantly higher in the bFF and KF groups relative to the other treatment groups, particularly in the bFF group. Estradiol and progesterone production were also highest in the bFF group, and primary follicle diameters were the largest. Up until D24, the bFF group still exhibited the highest proportion of developing follicles. In conclusion, the bFGF–FSH combination promotes nonhuman primate primordial follicle developmentin vitro, with the optimal experimental window within 18 days. These results provide evidence for the future success of human ovarian cortex culture and the eventual acquisition of mature human follicles or oocytes for fertility restoration.
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Edwards, J. E. Hocking, M. J. Birtles, P. M. Harris, et al. "Pre- and post-natal wool follicle development and density in sheep of five genotypes." Journal of Agricultural Science 126, no. 3 (1996): 363–70. http://dx.doi.org/10.1017/s002185960007492x.
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SUMMARYThe pre-natal and post-natal development of wool follicles in sheep of five genotypes with contrasting wool types was examined to provide data on which to base studies of physiological factors affecting wool type via follicle development. This study was conducted following Autumn mating in 1992 at Palmerston North, New Zealand (40° S, 176° E). The rate and timing of follicle development in midside skin samples from Romney, Merino, Merino × Romney (M × R), Drysdale and Wiltshire foetuses and lambs collected at weekly intervals from days 76 to 143 of gestation and 1, 3, 7, 12 and 32 weeks after birth were examined.Primary (P) follicle density had a similar pattern of development in each of the genotypes, although the Merino had a significantly greater density of P follicles than the other genotypes. There was a difference in the rate of P follicle maturation between genotypes with the Drysdale, Wiltshire and M × R completing P follicle maturation before the other two genotypes. However, the majority of P follicles in all genotypes were producing fibres by 111 days of gestation. It was concluded that the small differences in the density and time of development of the P follicles could not cause the differences in wool type between genotypes.The pattern of development of the secondary (S) follicle population was examined by comparing S: P ratios. The initiation of S follicles began at similar ages in the five genotypes, but initiation was completed earlier in the Romney, Drysdale and Wiltshire than in the Merino and M × R, as indicated by a significant genotype by age interaction (P < 0·001). There was no difference between genotypes in S:P ratio from 90 to 104 days of gestation. The S:P ratio of the Romney, Drysdale and Wiltshire did not change significantly from 104 days of gestation until the end of the study, indicating that few S follicles were initiated in these genotypes after 104 days of gestation. The M × R data showed a significant increase in S:P ratio until 119 days of gestation and the Merino S:P ratio increased until 126 days of gestation.The period between days 90 and 125 of gestation was identified as being the critical period for the development of different follicle populations in Merino and non-Merino genotypes and it is this period which should be the focus for studies to determine physiological factors controlling secondary follicle development.
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Liu, Jie, Shudi Dai, Zichun Dai, et al. "Transcriptome Profiling of Goose Ovarian Follicle Granulosa Cells Reveals Key Regulatory Networks for Follicle Selection." Animals 13, no. 13 (2023): 2132. http://dx.doi.org/10.3390/ani13132132.
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The selection of follicles determines the reproductive performance of birds, but the process of follicle selection in geese is still elusive. This study focuses on Yangzhou geese during the egg-laying period and divides the follicular development process into three stages: small follicle development, follicle selection, and follicle maturation. Transcriptome sequencing was performed on granulosa cells from large white follicles, small yellow follicles, and F5 and F4 follicles. In addition, we selected the transcripts that remained unchanged during the development and maturation of small follicles but significantly changed during the follicular selection stage as the transcript collection that plays an important role in the follicular selection process. Then, we performed functional analysis on these transcripts and constructed a ceRNA network. The results showed that during the follicular selection stage, the number of differentially expressed mRNAs, miRNAs, and lncRNAs was the highest. In addition, miR-222-3p, miR-2954-3p, miR-126-5p, miR-2478, and miR-425-5p are potential key core regulatory molecules in the selection stage of goose follicles. These results can provide a reference for a better understanding of the basic mechanisms of the goose follicle selection process and potential targets for the precise regulation of goose egg production performance.
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Schneyer, Alan L., Toshihiro Fujiwara, Janis Fox, et al. "Dynamic Changes in the Intrafollicular Inhibin/Activin/Follistatin Axis during Human Follicular Development: Relationship to Circulating Hormone Concentrations*." Journal of Clinical Endocrinology & Metabolism 85, no. 9 (2000): 3319–30. http://dx.doi.org/10.1210/jcem.85.9.6767.
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Abstract Previous studies of normal human ovaries suggest that inhibins, activins, and follistatin (FS) are produced in a stage-specific pattern indicative of intraovarian, autocrine/paracrine roles in regulating follicle development. However, these studies relied largely on surgical specimens and thus include little information about the menstrual cycle stage or dominant follicle status at the time follicles or ovaries were obtained. The purpose of this study was to 1) determine the pattern of intrafollicular hormone biosynthesis across antral follicle development in normal women, 2) compare hormone concentrations in dominant and nondominant follicles from the same ovary, and 3) examine the relationship between dominant follicle hormone content and circulating hormone levels. Intrafollicular estradiol, progesterone, and inhibin A concentrations increased significantly with follicle size or maturity, whereas significant inverse relationships were observed for androstenedione and the androstenedione/estradiol (A:E) ratio. In contrast, neither inhibin B, activin A, nor free FS varied consistently with size or maturity. Estradiol, progesterone, and inhibin A levels and A:E ratio were significantly lower in nondominant follicles compared to the dominant follicle aspirated from the same ovary. Although intrafollicular and serum concentrations of each hormone followed the same general pattern as follicles develop, the human follicular fluid/serum gradients changed during the follicular phase and were different for estradiol and inhibin A, suggesting the presence of stage-specific differences in pharmacodynamics. These results are consistent with the hypothesis that the orderly transition from an activin-dominant to an inhibin A/FS-dominant microenvironment is critical for dominant follicle development.
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Hornick, J. E., F. E. Duncan, L. D. Shea, and T. K. Woodruff. "Multiple follicle culture supports primary follicle growth through paracrine-acting signals." REPRODUCTION 145, no. 1 (2013): 19–32. http://dx.doi.org/10.1530/rep-12-0233.
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In vitro follicle growth in alginate hydrogels is a unique and versatile method for studying ovarian and follicle biology that may also have implications for fertility preservation. Current culture systems support the development of isolated mouse follicles from the secondary stage onward. However, it has been a challenge to grow smaller follicles in vitro due to the dissociation of the oocyte from companion somatic cells. Recent work has demonstrated that coculturing primary follicles with mouse embryonic fibroblasts or ovarian stromal cells supports follicle survival and growth. In this study, we demonstrate that follicles themselves can exert a beneficial coculture effect. When primary follicles were cultured in groups of five or ten (multiple follicle culture), there was increased growth and survival. The multiple follicle culture approach maintained follicle integrity and resulted in the formation of antral stage follicles containing meiotically competent gametes. The growth and survival of primary follicles were highly number dependent, with the most significant enhancement observed when the largest number of follicles was grown together. Our data suggest that the follicle unit is necessary to produce the secreted factors responsible for the supportive effects of multiple follicle culture, as neither denuded oocytes, oocyte-secreted factors, nor granulosa cells alone were sufficient to support early follicle growth in vitro. Therefore, there may be signaling from both the oocyte and the follicle that enhances growth but requires both components in a feedback mechanism. This work is consistent with current in vivo models for follicle growth and thus advances the movement to recapitulate the ovarian environment in vitro.
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McLaughlin, Eileen A., and Skye C. McIver. "Awakening the oocyte: controlling primordial follicle development." REPRODUCTION 137, no. 1 (2009): 1–11. http://dx.doi.org/10.1530/rep-08-0118.
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Oocytes are sequestered in primordial follicles before birth and remain quiescent in the ovary, often for decades, until recruited into the growing pool throughout the reproductive years. Therefore, activation of follicle growth is a major biological checkpoint that controls female reproductive potential. However, we are only just beginning to elucidate the cellular mechanisms required for either maintenance of the quiescent primordial follicle pool or initiation of follicle growth. Understanding the intracellular signalling systems that control oocyte maintenance and activation has significant implications for improving female reproductive productivity and longevity in mammals, and has application in domestic animal husbandry, feral animal population control and infertility in women.
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Duarte, Ana Beatriz Graça, Roberta Nogueira Chaves, Valdevane Rocha Araújo, et al. "Follicular interactions affect the in vitro development of isolated goat preantral follicles." Zygote 19, no. 3 (2010): 215–27. http://dx.doi.org/10.1017/s0967199410000237.
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SummaryThe aim of this study was to evaluate the influence of the number of follicles per drop (one or three) and antral follicles on in vitro development of isolated goat preantral follicles. Preantral follicles were isolated through microdissection and distributed individually (control) or in groups of three follicles (treatment) in microdroplets of α-MEM with or without 1000 ng/ml follicle stimulating hormone (FSH) for Experiments 1 and 2, respectively. Experiment 3 was divided into four treatments according to the presence of one or three preantral follicles, associated or not with antral follicles. After culture, oocytes were retrieved from morphologically normal follicles and submitted to in vitro maturation (IVM) and live/dead fluorescent labelling. Results of Experiment 1 (basic medium without FSH) showed that culture of preantral follicles in groups enhances viability, growth and antrum formation after 12 days. However, in the presence of FSH (Experiment 2), only the recovery rate of fully grown oocytes for IVM was significantly affected by grouping of follicles. In Experiment 3, in general, co-culture of preantral follicles with an early antral follicle had a detrimental effect on viability, antrum formation and production of oocytes for IVM. In conclusion, the performance of in vitro culture of goat preantral follicles is affected by the number of follicles per drop, the presence of an antral follicle and FSH.
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Vernunft, A., J. M. Weitzel, and T. Viergutz. "179 CORPUS LUTEUM DEVELOPMENT AFTER FOLLICLE ASPIRATION IS RELATED TO CHARACTERISTICS OF THE ASPIRATED FOLLICLE IN DAIRY COWS." Reproduction, Fertility and Development 25, no. 1 (2013): 238. http://dx.doi.org/10.1071/rdv25n1ab179.
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The aim of this study was to investigate whether morphology or function of a corpus luteum (CL), which developed after an aspiration of a preovulatory follicle, is related to follicular characteristics such as size or steroid content. If so, CL morphology or function could be used as a retrospective quality parameter for the aspirated follicle or the follicular characteristics as a prospective parameter for the quality of the developing CL. Therefore, 44 aspiration sessions were performed using 18 cows between 26 and 121 days after parturition during the first lactation. Heat was induced in mid-dioestrus with Cloprostenol. A GnRH analogon (Depherelin) were administrated 54 h later. The dominant follicle was aspirated 21 h after administration of the GnRH analogue. The diameter of the dominant follicle at aspiration and the cross-section area of the resulting luteal tissue 14 days later were measured by ultrasound. Concentrations of progesterone (P4) and 17-β-oestradiol (E2) in blood and follicular fluid (FF) were determined by H3-RIA. A CL development occurred in 82% of aspiration sessions after aspirating the dominant follicles. The interval of time between parturition and follicle aspiration did not affect variables investigated. As expected, cross-section area of the luteal tissue was positively correlated with plasma P4 concentration on Day 14 after follicle aspiration (r = 0.54; P < 0.01). The diameter of the aspirated follicle was positively correlated with the plasma P4 concentration on Day 14 after follicle aspiration (r = 0.52; P = 0.02), but the diameter was not correlated with the cross-section. Comparing the FF of follicles that originated a CL after aspiration with follicles that did not, both types had comparable P4 concentrations (578 ± 79 ng mL–1 v. 398 ± 84 ng mL–1; P = 0.2), but the former type presented higher E2 concentrations (206 ± 23 ng mL–1 v. 64 ± 29 ng mL–1, P < 0.01) compared with the latter. The P4 concentrations in FF of follicles that originated a CL after aspiration were positively related to cross-section area of the CL (r = 0.48; P = 0.04), but neither P4 nor E2 concentrations in the FF of preovulatory follicles could be used as a predictor for the plasma P4 concentration at day 14. In conclusion, CL development after follicle aspiration can be used as a retrospective quality parameter of aspirated dominant follicles. Preovulatory follicle diameter as well as cross-section area of the luteal tissue could be used prospectively to identify cows with high plasma P4 levels, and this may help to identify suitable recipients for embryo transfer. This study was supported by the German Research Foundation (DFG WE 2458/7-2).
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Austin, Publishing Group. "Follicle Aspirating is an Effective Remedy When Multi-follicles Developed in Donor-sperm Timing-Artificial Insemination." Austin Journal of Invitro Fertilization 7, no. 1 (2023): 1042. https://doi.org/10.26420/AustinJInVitroFertili.2023.1042.
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Abstract <strong>Purpose:</strong> To avoid multi-pregnancy, the cycle usually has to be cancelled when Multi-Follicles Developed (MFD) in artificial insemination. For the strong willing to continue the cycle for most patients, we explored the effectiveness of excess follicles aspirating as another remedy when multiple follicle developed. <strong>Methods:</strong> We conducted a retrospective study in patients taking Artificial Insemination with Donor sperm (AID) and ovarian stimulation protocol from 2011 to 2022. Patients were divided in 4 groups according to the differences of receiving aspirating and follicle number. Clinical pregnancy rate, multi-pregnancy rate (twin pregnancy and high order pregnancy, separately) were mainly compared in our study. <strong>Results:</strong> When multi-follicles developed, patients taking excess follicle aspirating achieved a comparable clinical pregnancy rate with those without aspirating (30.7% vs 26.1%). These two groups had a similar multi-pregnancy rate, 21.7% and 17.4% respectively, while high order pregnancy was rather lower in excess follicles aspirating group. MFD patients carried a significant higher clinical pregnancy rate, multi-pregnancy rate than patients with two dominate follicles patients under the age of 35. In ovarian stimulation protocol, patients with two dominate follicles carried nearly the same clinical pregnancy rate with one dominate follicle patients (21.4 vs 21.5%). Gemellary pregnancy rate was significant lower in one than two dominate follicles group (7.5% vs 0.4%) when patient’s age was under 35. In the age of 35 or older, the clinical pregnancy rate and multi-pregnancy rate were similar in patients with multi-follicles and two dominate follicles. <strong>Conclusion:</strong> In AID, in the age of lower than 35, when multi-follicles developed, excess follicle aspirating with two dominate follicles reserved effectively deceased high order pregnancy and ensured the clinical pregnancy rate at the same time. From the perspective of singleton, it was feasible to keep one dominate follicle reserved. <strong>Keywords:</strong> AID; Multi-follicle development; Multi-pregnancy rate; Follicle aspirating
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Liu, Jie, Conghui Guo, Junjie Fu, et al. "Identification and Functional Analysis of circRNAs during Goat Follicular Development." International Journal of Molecular Sciences 25, no. 14 (2024): 7548. http://dx.doi.org/10.3390/ijms25147548.
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Litter size is a crucial quantitative trait in animals, closely linked to follicular development. Circular RNA (circRNA), a type of single-stranded closed-loop endogenous RNA with stable expression, plays pivotal roles in various biological processes, yet its function in goat follicular development remains unclear. In this study, we collected large (follicle diameter > 3 mm) and small (1 mm < follicle diameter < 3 mm) follicles from black goats in the Chuanzhong region for circRNA sequencing, with the aim of elucidating the functional circRNAs that influence follicle development in goats. Differential analysis revealed that 17 circRNAs were upregulated in large follicles, and 28 circRNAs were upregulated in small follicles. Functional enrichment analysis revealed significant enrichment of pathways related to reproduction, including cellular response to follicle-stimulating hormone stimulus, the PI3K-Akt signaling pathway, the MAPK signaling pathway, and the Notch signaling pathway. Based on the ceRNA mechanism, 45 differentially expressed circRNAs were found to target and bind a total of 418 miRNAs, and an intercalation network including miR-324-3p (circRNA2497, circRNA5650), miR-202-5p (circRNA3333, circRNA5501), and miR-493-3p (circRNA4995, circRNA5508) was constructed. In addition, conservation analysis revealed that 2,239 circRNAs were conserved between goats and humans. Prediction of translation potential revealed that 154 circRNAs may potentially utilize both N6-methyladenosine (m6A) and internal ribosome entry site (IRES) translation mechanisms. Furthermore, the differential expression and circularization cleavage sites of five circRNAs were validated through RT-qPCR and DNA sequencing. Our study constructed a circRNA map in goat follicle development, offering a theoretical foundation for enhancing goat reproductive performance.
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Vernunft, A., JM Weitzel, and T. Viergutz. "Corpus luteum development and its morphology after aspiration of a preovulatory follicle is related to size and steroid content of the follicle in dairy cows." Veterinární Medicína 58, No. 4 (2013): 221–29. http://dx.doi.org/10.17221/6760-vetmed.
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Secretion of adequate levels of progesterone from a proper corpus luteum (CL), which develops out of the cells of a healthy preovulatory follicle, is a key-factor for establishment of a pregnancy. The aim of this study was to investigate the relationship between morphological and secretory characteristics of preovulatory follicles and their corresponding corpus luteum with regard to the post-partum period in high-yielding dairy cows. Therefore, ultrasound-guided aspirations of preovulatory follicles were performed repeatedly, using 20 first lactating cows between 26 and 121 days after parturition. Heat was induced with a PGF analogon followed by administration of a GnRH analogon. The dominant follicle was aspirated 21 h after administration of the GnRH analogon. The diameters of the follicles were estimated at aspiration and the morphology of the resulting luteal tissue was examined on day 14 after follicle aspiration using ultrasonographic examinations. Concentrations of progesterone (P<sub>4</sub>) and 17-beta-oestradiol (E<sub>2</sub>) were determined in the follicular fluids (FF) and P<sub>4</sub> concentration was estimated at the time of CL examination in plasma. A CL development occurred in 82% after dominant follicle aspiration. The interval of time between parturition and follicle aspiration did not affect the investigated variables. The diameter of the aspirated preovulatory follicle was positively correlated to the cross-section area of the developed luteal tissue (R = 0.60; P &lt; 0.01) as well as to the plasma P<sub>4</sub> concentration on day 14 after follicle aspiration (R = 0.47; P&nbsp;&lt; 0.05). Also, E<sub>2</sub> concentrations in FF were positively correlated to cross-section area of the luteal tissue (R = 0.54; P &lt; 0.05). Comparing the FF of the follicles that gave rise to a CL after aspiration to follicles that did not, both types had comparable P<sub>4</sub>, but the former type harboured higher E<sub>2</sub> concentrations. In conclusion, preovulatory follicle diameter as well as steroid concentrations in the follicular fluid could be used prospectively to identify cows which will have well-developed CLs and high plasma P<sub>4</sub> levels later. On the other hand, CL development after follicle aspiration can be used as a retrospective quality parameter of dominant follicles. These results will help to identify suitable animals for breeding or recipients for embryo transfer.&nbsp;&nbsp;&nbsp; &nbsp;
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Vlaisavljevic, V., and M. Došen. "Clinical Applications of Ultrasound in Assessment of Follicle Development and Growth." Donald School Journal of Ultrasound in Obstetrics and Gynecology 1, no. 2 (2007): 50–63. http://dx.doi.org/10.5005/jp-journals-10009-1099.
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Abstract Monitoring of individual follicles during the menstrual cycle demonstrates in a noninvasive way the changes in their number and position during the early and the late follicular phase and the luteal phase. The differences in relations between the follicles near the dominant follicle can be demonstrated with the same technique using 3D reconstruction of the ovary. An increased perifollicular blood flow can be measured in the perifollicular period using color and pulsed Doppler. Automated estimation of blood volume around the ovarian follicles brought a new concept to this area. Results confirm the observation that vascularity around the follicle is intense in the periovulatory period. The blood volume does not differ between follicles containing an oocyte and those with no oocyte in the aspirate, or a nonfertilizable oocyte. From our results we can hypothesize that those follicles containing oocytes able to produce pregnancy have a more uniform perifollicular vascular network . Recognition of the follicle growth pattern has a prognostic value for the outcome of assisted reproduction methods. Follicular diameter and changes in growth patterns are more important than follicular wall thickness as parameters having an impact on clinical success.
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Sato, Yorino, Yuan Cheng, Kazuhiro Kawamura, Seido Takae, and Aaron J. W. Hsueh. "C-Type Natriuretic Peptide Stimulates Ovarian Follicle Development." Molecular Endocrinology 26, no. 7 (2012): 1158–66. http://dx.doi.org/10.1210/me.2012-1027.
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Abstract C-type natriuretic peptide (CNP) encoded by the NPPC (Natriuretic Peptide Precursor C) gene expressed in ovarian granulosa cells inhibits oocyte maturation by activating the natriuretic peptide receptor (NPR)B (NPRB) in cumulus cells. RT-PCR analyses indicated increased NPPC and NPRB expression during ovarian development and follicle growth, associated with increases in ovarian CNP peptides in mice. In cultured somatic cells from infantile ovaries and granulosa cells from prepubertal animals, treatment with CNP stimulated cGMP production. Also, treatment of cultured preantral follicles with CNP stimulated follicle growth whereas treatment of cultured ovarian explants from infantile mice with CNP, similar to FSH, increased ovarian weight gain that was associated with the development of primary and early secondary follicles to the late secondary stage. Of interest, treatment with FSH increased levels of NPPC, but not NPRB, transcripts in ovarian explants. In vivo studies further indicated that daily injections of infantile mice with CNP for 4 d promoted ovarian growth, allowing successful ovulation induction by gonadotropins. In prepubertal mice, CNP treatment alone also promoted early antral follicle growth to the preovulatory stage, leading to efficient ovulation induction by LH/human chorionic gonadotropin. Mature oocytes retrieved after CNP treatment could be fertilized in vitro and developed into blastocysts, allowing the delivery of viable offspring. Thus, CNP secreted by growing follicles is capable of stimulating preantral and antral follicle growth. In place of FSH, CNP treatment could provide an alternative therapy for female infertility.
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Qi, Yan, Huiliang Xue, Jinhui Xu, Ming Wu, Lei Chen, and Laixiang Xu. "Effect of PACAP/PAC1R on Follicle Development of Djungarian Hamster (Phodopus sungorus) with the Variation of Ambient Temperatures." Biology 12, no. 2 (2023): 315. http://dx.doi.org/10.3390/biology12020315.
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In Phodopus sungorus, the relationship between pituitary adenylate cyclase-activating polypeptide (PACAP) and its receptor (PAC1R), follicle-stimulating hormone (FSH), and follicle development remains unclear. In this study, we found that the development of growing follicles and antral follicles were inhibited at low (8 °C, 14 °C) and high (29 °C) temperatures. Meanwhile, PACAP/PAC1R expression and follicle-stimulating hormone (FSH) serum concentration significantly decreased during ambient temperatures of 8 °C, 14 °C and 29 °C compared to 21 °C. Thus, ambient temperature may influence the expression of PACAP/PAC1R and the synthesis of FSH for involvement in follicle development. Moreover, PACAP/PAC1R had major functional elements including PKA/PKG and PKC phosphorylation sites, which may involve in the pathway of FSH synthesis through cAMP-PKA and its downstream signal pathway. Moreover, there was a significant positive correlation between the expression levels of PACAP/PAC1R and the number of the growing and antral follicles, as well as the serum FSH concentration and the number of antral follicles. However, there was no significant correlation between the expression levels of PACAP/PAC1R and the serum FSH concentration, indicating a complicated pathway between PACAP/PAC1R and FSH. In conclusion, ambient temperature affects the expression of PACAP/PAC1R and the serum FSH concentration. The expression of PACAP/PAC1R and the serum FSH concentration are correlated with follicle development, which implies that they are involved in follicle development, which will ultimately influence the reproduction of Phodopus sungorus. This study can lay the foundation for future investigation on the regulation mechanism of reproduction in Phodopus sungorus.
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Luo, Gang, Ruiguang Gong, Yaotian Ai, Tongyan Zhu, and Zhanjun Ren. "Identification of N6-Methyladenosine-Related Factors and the Prediction of the Regulatory Mechanism of Hair Follicle Development in Rex and Hycole Rabbits." Biology 12, no. 11 (2023): 1448. http://dx.doi.org/10.3390/biology12111448.
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Hair follicle development directly affects the development of the rabbit fur industry. The growth and development of a hair follicle is modified and regulated by many genes and mechanisms. M6A is an important RNA modification. However, there are few studies on the effects of the regulation of m6A on hair follicle growth and development. In this study, hematoxylin–eosin (HE) staining was used to explore the difference in hair follicle development between Rex rabbits and Hycole rabbits, and we performed m6A sequencing to identify the key genes with m6A modification in hair follicle growth. The results showed that the hair length, coarse hair percentage, primary hair follicle ratio, and skin thickness of Hycole rabbits were significantly higher than those of Rex rabbits. However, the proportion of secondary hair follicles in Hycole rabbits was significantly lower than that in Rex rabbits. In addition, we found five differential methylases, 20 differential genes, and 24 differential signaling pathways related to hair growth and development. The results of the Sankey diagram showed that 12 genes were related to 13 signal pathways. Finally, we found that five methylases regulated the development of hair follicles through differential genes/signal pathways. These findings laid a molecular foundation for the function of m6A modification in hair development.
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Chen, Yaru, Yan Wu, Jinsong Pi та ін. "tsRNA-00764 Regulates Estrogen and Progesterone Synthesis and Lipid Deposition by Targeting PPAR-γ in Duck Granulosa Cells". International Journal of Molecular Sciences 25, № 20 (2024): 11251. http://dx.doi.org/10.3390/ijms252011251.
Full textAbstract:
Transfer RNA-derived small RNAs (tsRNAs) are novel regulatory small non-coding RNAs that have been found to modulate many life activities in recent years. However, the exact functions of tsRNAs in follicle development remain unclear. Follicle development is a remarkably complex process that follows a strict hierarchy and is strongly associated with reproductive performance in ducks. The process of converting small yellow follicles into hierarchal follicles is known as follicle selection, which directly determines the number of mature follicles. We performed small RNA sequencing during follicle selection in ducks and identified tsRNA-00764 as the target of interest based on tsRNA expression profiles in this study. Bioinformatics analyses and luciferase reporter assays further revealed that peroxisome proliferator-activated receptor-γ (PPAR-γ) was the target gene of tsRNA-00764. Moreover, tsRNA-00764 knockdown promoted estrogen and progesterone synthesis and lipid deposition in duck granulosa cells, while a PPAR-γ inhibitor reversed the above phenomenon. Taken together, these results demonstrate that tsRNA-00764, differentially expressed in pre-hierarchal and hierarchy follicles, modulates estrogen and progesterone synthesis and lipid deposition by targeting PPAR-γ in duck granulosa cells, serving as a potential novel mechanism of follicle selection. Overall, our findings provide a theoretical foundation for further exploration of the molecular mechanisms underlying follicle development and production performance in ducks.
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Dalgleish, Elizabeth. "Effectiveness of Invertebrate and Vertebrate Pollinators and the Influence of Pollen Limitation and Inflorescence Position on Follicle Production of Banksia aemula (Family Proteaceae)." Australian Journal of Botany 47, no. 4 (1999): 553. http://dx.doi.org/10.1071/bt97070.
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Follicle development of Banksia aemula (R.Brown 1810) was studied in northern New South Wales, Australia, after exposure of inflorescences to different combinations of pollinator type and pollen quantity. When inflorescences within plants were exposed to all pollinators and provided with additional cross-pollen, follicle development was increased, suggesting that B. aemula was pollen-limited. The addition of cross-pollen did not increase follicle development when inflorescences within plants were exposed to invertebrate pollination only. Nor did exclusion of vertebrates significantly reduce follicle development of plants relative to that of others which were exposed to all pollinators. The vegetation surrounding plants influenced the follicle development of inflorescences, and inflorescences in peripheral positions had more follicles than inflorescences that were internal.
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Cossigny, Davina A., Jock K. Findlay, and Ann E. Drummond. "The effects of FSH and activin A on follicle development in vitro." REPRODUCTION 143, no. 2 (2012): 221–29. http://dx.doi.org/10.1530/rep-11-0105.
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Numerous studies have reported on the roles of activins in gonadal regulation; however, little is known about their specific roles in early folliculogenesis. Ovarian follicular growth was investigated in 10-day cultures of day 4 postnatal whole ovaries treated with activin A (ActA; 50 ng/ml), with or without FSH (100 ng/ml) in vitro. We hypothesized that treatment with ActA±FSH would affect rates of growth and atresia in follicles. None of the treatments affected primordial follicle activation, and antral follicles were not observed after 10 days in culture. Primordial follicle numbers from all treatment groups were ∼20% of those in day 4 fresh ovaries, indicating that activation had occurred. In the presence of ActA, preantral follicle numbers increased significantly (P<0.0001). ActA alone decreased the proportion of atretic follicles in the primary and preantral classes, whereas the combined treatment of ActA+FSH increased the proportion of atretic preantral oocytes. Real-time PCR analysis revealed that follistatin, FSH receptor, and activin βA and βB subunits were all expressed at significantly higher levels in the ActA-only treated group but not in the ActA+FSH group. Here, we report novel findings supporting the role of FSH in primordial follicle survival through an action on apoptosis and a stimulatory role of ActA in the primordial to primary and preantral stages of follicle development, suggesting an inhibitory action of activin on oocyte apoptosis.
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Orisaka, Makoto, Katsushige Hattori, Shin Fukuda, et al. "Dysregulation of Ovarian Follicular Development in Female Rat: LH Decreases FSH Sensitivity During Preantral-Early Antral Transition." Endocrinology 154, no. 8 (2013): 2870–80. http://dx.doi.org/10.1210/en.2012-2173.
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Abstract Several clinical studies have shown a correlation of hypersecretion of LH and polycystic ovary syndrome (PCOS), infertility, and miscarriage in women, suggesting that chronically elevated LH impairs fertility. Growth arrest of small antral follicles in PCOS is also assumed to be associated with an abnormal endocrine environment involving increased LH stimulation, a hyperandrogenic milieu, and subsequent dysregulated FSH action in the ovarian follicles. In this study, we examined whether and how LH modulates follicular development and steroid production during preantral-early antral follicle transition by using a rat preantral follicle culture system. LH augments testosterone and estradiol production in preantral follicles via up-regulating mRNA abundance of CYP17A1 and CYP19A1. LH promotes rat preantral follicle growth, and the follicular size reaches that of early antral follicles in vitro, a response attenuated by the specific androgen receptor antagonist and a targeted disruption of androgen receptor gene. Sustained follicle stimulation by LH, but not by androgen, decreases FSH receptor mRNA levels and FSH receptor signaling and inhibits FSH-induced follicular growth. The data suggest that LH promotes preantral-early antral transition via the increased synthesis and growth-promoting action of androgen. However, chronic LH stimulation impairs FSH-dependent antral follicle growth by suppressing granulosa cell FSHR expression via the modulation of intraovarian regulators, including LH-induced thecal factors.
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Parry, AL, BW Norton, and BJ Restall. "Skin follicle development in the Australian cashmere goat." Australian Journal of Agricultural Research 43, no. 4 (1992): 857. http://dx.doi.org/10.1071/ar9920857.
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Follicle densities, S/P ratios and follicle number indices (FNI) of fibre-bearing primary (Pf) and secondary (Sf) follicles, and body weights, were taken sequentially on 224 kids at birth and at mean ages of 57, 107 and 301 days. All primary follicles but few secondary follicles were mature (fibre-bearing) at birth and Sf number increased 10 fold in the first 57 days after birth. A decline in Pf number was recorded between 57 and 107 days of age. SFNI's, but not Sf density increased to weaning (107 days of age) then declined thereafter to 301 days of age. Single kids had higher (P < 0.01) SFNI than twin kids at all ages except birth, though Sf/Pf ratios of singles were significantly higher (P < 0.05) than those of twins at 57 days of age only. At 107 and,301 days of age, males had higher PFNI than females (24.8 v. 22.0 and 24-7 v. 22.0) and higher SFNI than females (179.0 v. 150.4 and 151.6 v. 131-1). Sex differences were not observed in Sf/Pf ratio. A description of follicle arrangement and accessory structures is given.
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Sontakke, Sadanand D., Bushra T. Mohammed, Alan S. McNeilly, and F. Xavier Donadeu. "Characterization of microRNAs differentially expressed during bovine follicle development." REPRODUCTION 148, no. 3 (2014): 271–83. http://dx.doi.org/10.1530/rep-14-0140.
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Several different miRNAs have been proposed to regulate ovarian follicle function; however, very limited information exists on the spatiotemporal patterns of miRNA expression during follicle development. The objective of this study was to identify, using microarray, miRNA profiles associated with growth and regression of dominant-size follicles in the bovine monovular ovary and to characterize their spatiotemporal distribution during development. The follicles were collected from abattoir ovaries and classified as small (4–8 mm) or large (12–17 mm); the latter were further classified as healthy or atretic based on estradiol and CYP19A1 levels. Six pools of small follicles and individual large healthy (n=6) and large atretic (n=5) follicles were analyzed using Exiqon's miRCURY LNA microRNA Array 6th gen, followed by qPCR validation. A total of 17 and 57 sequences were differentially expressed (greater than or equal to twofold; P<0.05) between large healthy and each of small and large atretic follicles respectively. Bovine miRNAs confirmed to be upregulated in large healthy follicles relative to small follicles (bta-miR-144, bta-miR-202, bta-miR-451, bta-miR-652, and bta-miR-873) were further characterized. Three of these miRNAs (bta-miR-144, bta-miR-202, and bta-miR-873) were also downregulated in large atretic follicles relative to large healthy follicles. Within the follicle, these miRNAs were predominantly expressed in mural granulosa cells. Further, body-wide screening revealed that bta-miR-202, but not other miRNAs, was expressed exclusively in the gonads. Finally, a total of 1359 predicted targets of the five miRNAs enriched in large healthy follicles were identified, which mapped to signaling pathways involved in follicular cell proliferation, steroidogenesis, prevention of premature luteinization, and oocyte maturation.
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Bagg, Melanie A., Mark B. Nottle, David T. Armstrong, and Christopher G. Grupen. "Relationship between follicle size and oocyte developmental competence in prepubertal and adult pigs." Reproduction, Fertility and Development 19, no. 7 (2007): 797. http://dx.doi.org/10.1071/rd07018.
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The present study compared the distribution and steroid composition of 3-, 4- and 5–8-mm follicles on the surface of prepubertal and adult ovaries, and determined the relationship between follicle size and developmental competence of oocytes following parthenogenetic activation. The effect of 1 mm dibutyryl cAMP (dbcAMP) for the first 22 h of in vitro maturation (IVM) on the embryo development of prepubertal oocytes from the three follicle size cohorts was also determined. Compared with adult, prepubertal ovaries contained a higher proportion of 3-mm follicles (46 v. 72%, respectively), but a lower proportion of 4-mm (33 v. 22%, respectively) and 5–8-mm follicles (21 v. 6%, respectively). Adult follicular fluid (FF) contained 11-fold higher levels of progesterone (P4) than prepubertal FF, with similar levels observed between all adult follicle sizes. In prepubertal FF, the P4 concentration increased with follicle size from 3 to 4 to 5–8 mm. Rates of blastocyst development following parthenogenetic activation of adult oocytes from all three follicles sizes were similar (approximately 55%), whereas rates from prepubertal oocytes increased with increasing follicle size from 3 (17%) to 4 (36%) to 5–8 mm (55%). Treatment with dbcAMP for the first 22 h of IVM led to a 1.5-fold increase in the rate of blastocyst development for prepubertal oocytes from 3-mm follicles, but had no effect on prepubertal oocytes from the 4 and 5–8 mm classes. Mean blastocyst cell number increased with follicle size in prepubertal ovaries and was similar for all follicle sizes in adult ovaries. The present study demonstrates that the low efficiency of in vitro embryo production observed using prepubertal compared with adult pig oocytes is due to a greater proportion of 3-mm follicles on prepubertal ovaries, which contain oocytes of inferior developmental competence.
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Rose, Bruce I., and Samuel E. Brown. "A review of the physiology behind letrozole applications in infertility: are current protocols optimal?" Journal of Assisted Reproduction and Genetics 37, no. 9 (2020): 2093–104. http://dx.doi.org/10.1007/s10815-020-01892-6.
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Abstract Letrozole is a targeted aromatase inhibitor which has primarily been used in post-menopausal women with breast cancer. Recently, it has been utilized in infertile pre-menopausal women because of its ability to enhance FSH production for ovulation induction. However, the ovarian follicle’s response to FSH is only a part of the endocrine events occurring in a developing follicle. The health of the small antral follicles is driven primarily by androgens, which contribute to granulosa cell mitosis, sensitivity to FSH, and resistance to atresia. In contrast, elevated androgens in the late antral to pre-ovulatory follicle have a negative impact on follicle health and lead to atresia and cystic follicle formation. This ovarian physiologic data suggests that current applications of letrozole to infertility may be squandering some of the primary benefits available in using letrozole to promote follicle development. Four applications of letrozole to infertility that have appeared in the medical literature are reviewed. Androgen-related benefits are reviewed and various questions put forward about how letrozole could be more effectively used to help patients in these settings.
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Kaune, Heidy, Sairah Sheikh, and Suzannah A. Williams. "Analysis of in vitro follicle development during the onset of premature ovarian insufficiency in a mouse model." Reproduction, Fertility and Development 29, no. 8 (2017): 1538. http://dx.doi.org/10.1071/rd15524.
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Premature ovarian insufficiency (POI) occurs in 1% of women under 40 years of age and is predominantly idiopathic. In a transgenic mouse model of follicular POI, the Double Mutant (DM), female mice are fertile at 6 weeks of age, become infertile by 9 weeks and exhibit POI by 3 months. DM female mice generate oocytes lacking mucin O-glycans and complex N-glycans due to deletion of core 1 synthase, glycoprotein-N-acetylgalactosamine 3-β-galactosyltransferase 1 (C1galt1) and mannoside acetylglucosaminyltransferase 1 (Mgat1) respectively (DM, C1galt1F/FMgat1F/F:ZP3Cre; Control, C1galt1F/FMgat1F/F). To determine whether DM follicle development could be improved in a controlled environment, follicles from DM and Control mice were cultured individually and follicle growth, morphology, survival and antrum formation were evaluated. DM ovaries were more rigid than Control ovaries at 3, 6 and 9 weeks, which was exacerbated with age, resulting in a failure to isolate follicles from 9 week-old DM females. DM follicles had decreased survival compared with Control follicles from females at 3 and 6 weeks of age. Furthermore, survival rate of DM follicles decreased with age between 3 and 6 weeks. DM follicles at both 3 and 6 weeks had accelerated follicle growth and altered antrum formation during the first few days of culture but, after 6 days, follicles were equivalent in size to the Controls. In conclusion, a population of DM follicles retain the potential to develop in vitro, and therefore follicle culture offers a reliable method to generate antral follicles from preantral follicles after the onset of POI in these female mice.
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Xu, Mengmeng, Long Che, Zhenguo Yang, et al. "Proteomic Analysis of Fetal Ovaries Reveals That Primordial Follicle Formation and Transition Are Differentially Regulated." BioMed Research International 2017 (2017): 1–11. http://dx.doi.org/10.1155/2017/6972030.
Full textAbstract:
Primordial follicle formation represents a critical phase of the initiation of embryonic reproductive organ development, while the primordial follicle transition into primary follicle determines whether oestrus or ovulation will occur in female animals. To identify molecular mechanism of new proteins which are involved in ovarian development, we employed 2D-DIGE to compare the protein expression profiles of primordial follicles and primary follicles of fetal ovaries in pigs. Fetal ovaries were collected at distinct time-points of the gestation cycle (g55 and g90). The identified proteins at the g55 time-point are mainly involved in the development of anatomical structures [reticulocalbin-1 (RCN1), reticulocalbin-3 (RCN3)], cell differentiation (actin), and stress response [heterogeneous nuclear ribonucleoprotein K (HNRNPK)]. Meanwhile, at the g90 stage, the isolated proteins with altered expression levels were mainly associated with cell proliferation [major vault protein (MVP)] and stress response [heat shock-related 70 kDa protein 2 (HSPA2)]. In conclusion, our work revealed that primordial follicle formation is regulated by RCN1, RCN3, actin, and HNRNPK, while the primordial follicle transformation to primary follicle is regulated by MVP and HSPA2. Therefore, our results provide further information for the prospective understanding of the molecular mechanism(s) involved in the regulation of the ovarian follicle development.