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Journal articles on the topic 'Oviductin'

Author: Grafiati

Published: 4 June 2021

Last updated: 5 February 2022

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1

Marnier, C., M. Saint-Dizier, M. Z. Tahir, S. Chastant-Maillard, and K. Reynaud. "148 EXPRESSION OF OVIDUCT-SPECIFIC GLYCOPROTEIN IN THE CANINE OVIDUCT DURING THE PERIOVULATORY PERIOD." Reproduction, Fertility and Development 26, no. 1 (2014): 187. http://dx.doi.org/10.1071/rdv26n1ab148.

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In the canine species, the oocyte is ovulated at the immature germinal vesicle (GV) stage and will reach metaphase II stage after 3 to 4 days spent in the oviduct. Fertilization and embryonic development to the blastocyst stage also take place in the oviduct. In a previous study (Tahir et al. 2012 Reprod. Domest. Anim. 47, 487), we reported the expression of oviductin (oviduct-specific glycoprotein) mRNA in the oviduct. The present study aimed to describe the oviductin protein expression (immunolocalization and Western blot quantification) and the effect of the oviducal region and the ovarian

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2

Malette, B., and G. Bleau. "Biochemical characterization of hamster oviductin as a sulphated zona pellucida-binding glycoprotein." Biochemical Journal 295, no. 2 (1993): 437–45. http://dx.doi.org/10.1042/bj2950437.

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Oviductins are a family of glycoproteins, synthesized and released by oviductal secretory cells, which bind to the zona pellucida of the oocyte after ovulation. Hamster oviductin migrates as diffuse species of 160-350 kDa during SDS/PAGE under reducing as well as non-reducing conditions. In this report, we describe the one-step purification of hamster oviductin using either immuno- or lectin-affinity chromatography. Probing with specific lectins showed that the glycoprotein contains terminal alpha-D-GalNAc, and either terminal alpha-D-NeuAc or non-terminal beta-D-(GlcNAc)2 residues, but fails

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3

Barrera, Daniel, Pablo A. Valdecantos, E. Vanesa García, and Dora C. Miceli. "Cloning and sequence analysis of Bufo arenarum oviductin cDNA and detection of its orthologous gene expression in the mouse female reproductive tract." Zygote 20, no. 1 (2010): 17–26. http://dx.doi.org/10.1017/s0967199410000468.

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SummaryThe glycoprotein envelope surrounding the Bufo arenarum egg exists in different functional forms. Conversion between types involves proteolysis of specific envelope glycoproteins. When the egg is released from the ovary, the envelope cannot be penetrated by sperm. Conversion to a penetrable state occurs during passage through the pars recta portion of the oviduct, where oviductin, a serine protease with trypsin-like substrate specificity, hydrolyzes two kinds of envelope glycoproteins: gp84 and gp55. The nucleotide sequence of a 3203 bp B. arenarum oviductin cDNA was obtained. Deduced a

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4

González-Brusi, Leopoldo, Blanca Algarra, Carla Moros-Nicolás, Mª José Izquierdo-Rico, Manuel Avilés, and Maria Jiménez-Movilla. "A Comparative View on the Oviductal Environment during the Periconception Period." Biomolecules 10, no. 12 (2020): 1690. http://dx.doi.org/10.3390/biom10121690.

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The oviduct plays important roles in reproductive events: sperm reservoir formation, final gamete maturation, fertilization and early embryo development. It is well known that the oviductal environment affects gametes and embryos and, ultimately, the health of offspring, so that in vivo embryos are better in terms of morphology, cryotolerance, pregnancy rates or epigenetic profile than those obtained in vitro. The deciphering of embryo–maternal interaction in the oviduct may provide a better understanding of the embryo needs during the periconception period to improve reproductive efficiency.

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5

Ling, Ling, Yin-Lau Lee, Kai-Fai Lee, Sai-Wah Tsao, William S. B. Yeung, and Frederick W. K. Kan. "Expression of human oviductin in an immortalized human oviductal cell line." Fertility and Sterility 84 (October 2005): 1095–103. http://dx.doi.org/10.1016/j.fertnstert.2005.06.006.

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6

St-Jacques, Sylvie, Brigitte Malette, Simone Chevalier, Kenneth D. Roberts, and Gilles Bleau. "The zona pellucida binds the mature form of an oviductal glycoprotein (oviductin)." Journal of Experimental Zoology 262, no. 1 (1992): 97–104. http://dx.doi.org/10.1002/jez.1402620113.

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7

Briton-Jones, Christine, Ingrid Hung Lok, Pong Mo Yuen, Tony Tak Yu Chiu, Lai Ping Cheung, and Christopher Haines. "Human oviductin mRNA expression is not maintained in oviduct mucosal cell culture." Fertility and Sterility 77, no. 3 (2002): 576–80. http://dx.doi.org/10.1016/s0015-0282(01)03216-2.

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8

Roux, Emmanuelle, Gilles Bleau, and Frederick W. K. Kan. "Fate of hamster oviductin in the oviduct and uterus during early gestation." Molecular Reproduction and Development 46, no. 3 (1997): 306–17. http://dx.doi.org/10.1002/(sici)1098-2795(199703)46:3<306::aid-mrd9>3.0.co;2-t.

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9

Wagh, Premanand V., and Jack Lippes. "Human oviductal fluid proteins. V. Identification of human oviductin-I as alpha-fetoprotein." Fertility and Sterility 59, no. 1 (1993): 148–56. http://dx.doi.org/10.1016/s0015-0282(16)55631-3.

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10

Rottmayer, Regine, Susanne E. Ulbrich, Sabine Kölle, et al. "A bovine oviduct epithelial cell suspension culture system suitable for studying embryo–maternal interactions: morphological and functional characterization." Reproduction 132, no. 4 (2006): 637–48. http://dx.doi.org/10.1530/rep.1.01136.

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We established a short-term (24 h) culture system for bovine oviduct epithelial cells (BOECs), obtained on day 3.5 of the estrous cycle and evaluated the cells with respect to morphological criteria, marker gene expression, and hormone responsiveness. BOEC sheets were isolated mechanically from the ampulla with similar yields from oviducts ipsi- and contralateral to the ovulation site (57.9 ± 4.6 and 56.4 ± 8.0 × 106cells). BOECs showed > 95% purity and cells cultured for 24 h maintained morphological characteristics presentin vivo, as determined by light microscopy, scanning electron micro

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11

Zhao, Yuewen, Xiaojing Yang, Zongchao Jia, Robert L. Reid, Pierre Leclerc, and Frederick W. K. Kan. "Recombinant human oviductin regulates protein tyrosine phosphorylation and acrosome reaction." Reproduction 152, no. 5 (2016): 561–73. http://dx.doi.org/10.1530/rep-16-0177.

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The mammalian oviduct synthesizes and secretes a major glycoprotein known as oviductin (OVGP1), which has been shown to interact with gametes and early embryos. Here we report the use of recombinant DNA technology to produce, for the first time, the secretory form of human OVGP1 in HEK293 cells. HEK293 colonies stably expressing recombinant human OVGP1 (rHuOVGP1) were established by transfecting cells with an expression vector pCMV6-Entry constructed with OVGP1 cDNA. Large quantities of rHuOVGP1 were obtained from the stably transfected cells using the CELLSPIN cell cultivation system. A two-s

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12

Hendrix, Ericka, Aveline Hewetson, Malini Mansharamani, and Beverly S. Chilton. "Oviductin (Muc9) Is Expressed in Rabbit Endocervix." Endocrinology 142, no. 5 (2001): 2151–54. http://dx.doi.org/10.1210/endo.142.5.8285.

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13

Merlen, Yannick, and Gilles Bleau. "Organization of a gene coding for an oviduct-specific glycoprotein (oviductin) in the hamster." Molecular Reproduction and Development 57, no. 3 (2000): 238–46. http://dx.doi.org/10.1002/1098-2795(200011)57:3<238::aid-mrd5>3.0.co;2-r.

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14

Georgiou, A. S., E. Sostaric, C. H. Wong, et al. "293. Gametes alter the oviductal secretory proteome in vivo." Reproduction, Fertility and Development 17, no. 9 (2005): 124. http://dx.doi.org/10.1071/srb05abs293.

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We sought to identify altered oviductal protein secretions in response to the presence of gametes in the oviduct in vivo at the time of ovulation. Experiments were designed to compare oviductal fluid from a gamete-stimulated oviduct to a non-gamete-stimulated oviduct within the same animal. Clips were introduced at the infundibulum of both oviducts to prevent oocytes from entering the oviducts and one uterine horn was cut to prevent sperm access to that oviduct. Sows were artificially inseminated the next day with diluted boar semen. Control sows that had undergone the same surgical procedures

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15

Simintiras, Constantine A., Thomas Fröhlich, Thozhukat Sathyapalan, et al. "Modelling aspects of oviduct fluid formation in vitro." Reproduction 153, no. 1 (2017): 23–33. http://dx.doi.org/10.1530/rep-15-0508.

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Oviduct fluid is the microenvironment that supports early reproductive processes including fertilisation, embryo cleavage and genome activation. However, the composition and regulation of this critical environment remain rather poorly defined. This study uses anin vitropreparation of the bovine oviduct epithelium to investigate the formation and composition ofin vitro-derived oviduct fluid (ivDOF) within a controlled environment. We confirm the presence of oviduct-specific glycoprotein 1 inivDOF and show that the amino acid and carbohydrate content resembles that of previously reportedin vivod

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16

Briton-Jones, Christine, Ingrid Hung Lok, Che Kwok Cheung, Tony Tak Yu Chiu, Lai Ping Cheung, and Christopher Haines. "Estradiol regulation of oviductin/oviduct-specific glycoprotein messenger ribonucleic acid expression in human oviduct mucosal cells in vitro." Fertility and Sterility 81 (March 2004): 749–56. http://dx.doi.org/10.1016/j.fertnstert.2003.08.016.

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17

Briton-Jones, C. "Regulation of human oviductin mRNA expression in vivo." Fertility and Sterility 75, no. 5 (2001): 942–46. http://dx.doi.org/10.1016/s0015-0282(01)01696-x.

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18

Malette, Brigitte, Benoit Filion, Sylvie St-Jacques, Frederick W. K. Kan, and Gilles Bleau. "Hormonal control of the biosynthesis of hamster oviductin." Microscopy Research and Technique 31, no. 6 (1995): 470–77. http://dx.doi.org/10.1002/jemt.1070310603.

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19

Li, Hang Wu Raymond, Subin Liao, Philip Chi Ngong Chiu, et al. "Expression of Adrenomedullin in Human Oviduct, Its Regulation by the Hormonal Cycle and Contact with Spermatozoa, And Its Effect on Ciliary Beat Frequency of the Oviductal Epithelium." Molecular Endocrinology 24, no. 7 (2010): 1499. http://dx.doi.org/10.1210/mend.24.7.9999.

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Abstract Context: Adrenomedullin (ADM) has been found expressed in the mouse oviduct and might play a role in reproduction. Objective: To demonstrate the expression of adrenomedullin (ADM) in the human oviduct, investigate its regulation by steroidal hormones and spermatozoa contact, and study its effect on ciliary beat frequency (CBF) in the human oviduct. Design, Setting, Patients and Interventions: Oviducts from women undergoing hysterectomy for benign diseases in a university hospital were collected. The oviducts were treated with estradiol and/or progesterone to simulate different phases

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20

Kan, Frederick W. K., and Emmanuelle Roux. "Elaboration of an oviductin by the oviductal epithelium in relation to embryo development as visualized by immunocytochemistry." Microscopy Research and Technique 31, no. 6 (1995): 478–87. http://dx.doi.org/10.1002/jemt.1070310604.

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21

Briton-Jones, C. M., I. H. Lok, T. T. Chiu, P. M. Yuen, L. P. Cheung, and C. J. Haines. "Variation in Oviductin mRNA Expression Throughout the Ovulatory Cycle." Fertility and Sterility 74, no. 3 (2000): S130—S131. http://dx.doi.org/10.1016/s0015-0282(00)01091-8.

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22

Lee, Kai-Fai, Jia-Sen Xu, Yin-Lau Lee, and William S. B. Yeung. "Demilune Cell and Parotid Protein from Murine Oviductal Epithelium Stimulates Preimplantation Embryo Development." Endocrinology 147, no. 1 (2006): 79–87. http://dx.doi.org/10.1210/en.2005-0596.

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In mammals, fertilization and early preimplantation embryo development occur in the oviduct. We hypothesized that interaction exists between the developing embryos and the maternal genital tract, such that the embryos modulate the physiology and gene expression of the oviduct so that it is conducive to their development. By comparing the gene expression patterns in mouse oviducts containing transferred preimplantation embryos with those of oviducts containing oocytes, we report here the characterization of demilune cell and parotid protein (Dcpp), which was up-regulated in the embryo-containin

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23

Lapointe, Jérome, Monica Roy, Isabelle St-Pierre, et al. "Hormonal and Spatial Regulation of Nitric Oxide Synthases (NOS) (Neuronal NOS, Inducible NOS, and Endothelial NOS) in the Oviducts." Endocrinology 147, no. 12 (2006): 5600–5610. http://dx.doi.org/10.1210/en.2005-1548.

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Nitric oxide (NO) is a free radical produced by the action of NO synthases (NOS) and is known to be involved in the regulation of many reproductive events that occur in the oviducts. The oviducts are highly specialized organs that play crucial roles in reproduction by providing an optimal environment for the final maturation of gametes, fertilization, and early embryo development. In this study, we analyzed the expression, hormonal regulation, and cellular distribution of neuronal, inducible, and endothelial NOS in different bovine oviduct segments to better understand the roles played by thes

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24

Barrera, Daniel, Ricardo J. Llanos, and Dora C. Miceli. "Participation of the 39-kDa glycoprotein (gp39) of the vitelline envelope of Bufo arenarum eggs in sperm–egg interaction." Zygote 20, no. 2 (2011): 159–71. http://dx.doi.org/10.1017/s0967199411000049.

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SummaryThe acquisition of egg fertilizability in Bufo arenarum takes place during the oviductal transit and during this process the extracellular coelomic envelope (CE) of the eggs is converted into the vitelline envelope (VE). It has been stated that one of the necessary events leading to a fertilizable state is the proteolytic cleavage of CE glycoproteins in the oviductal pars recta by oviductin, a serine protease. Consequently, there is a marked increase in the relative quantity of glycoproteins with 39 (gp39) and 42 kDa (gp42) in the VE. In the present study, sperm–VE binding assays using

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25

Briton-Jones, Christine, Ingrid Hung Lok, Tony Tak Yu Chiu, Lai Ping Cheung та Christopher Haines. "Human chorionic gonadotropin and 17-β estradiol regulation of human oviductin/oviduct specific glycoprotein mRNA expression in vitro". Fertility and Sterility 80 (вересень 2003): 720–26. http://dx.doi.org/10.1016/s0015-0282(03)00771-4.

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26

Bridges, Phillip J., Myoungkun Jeoung, Sarah Shim, et al. "Hematopoetic Prostaglandin D Synthase: An ESR1-Dependent Oviductal Epithelial Cell Synthase." Endocrinology 153, no. 4 (2012): 1925–35. http://dx.doi.org/10.1210/en.2011-1900.

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Oviductal disease is a primary cause of infertility, a problem that largely stems from excessive inflammation of this key reproductive organ. Our poor understanding of the mechanisms regulating oviductal inflammation restricts our ability to diagnose, treat, and/or prevent oviductal disease. Using mice, our objective was to determine the spatial localization, regulatory mechanism, and functional attributes of a hypothesized regulator of oviductal inflammation, the hematopoietic form of prostaglandin D synthase (HPGDS). Immunohistochemistry revealed specific localization of HPGDS to the oviduct

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27

Banliat, Charles, Guillaume Tsikis, Valérie Labas, et al. "Identification of 56 Proteins Involved in Embryo–Maternal Interactions in the Bovine Oviduct." International Journal of Molecular Sciences 21, no. 2 (2020): 466. http://dx.doi.org/10.3390/ijms21020466.

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The bovine embryo develops in contact with the oviductal fluid (OF) during the first 4–5 days of pregnancy. The aim of this study was to decipher the protein interactions occurring between the developing embryo and surrounding OF. In-vitro produced 4–6 cell and morula embryos were incubated or not (controls) in post-ovulatory OF (OF-treated embryos) and proteins were then analyzed and quantified by high resolution mass spectrometry (MS) in both embryo groups and in OF. A comparative analysis of MS data allowed the identification and quantification of 56 embryo-interacting proteins originated f

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28

Maillo, Veronica, Maria Jesus Sánchez-Calabuig, Ricaurte Lopera-Vasquez, et al. "Oviductal response to gametes and early embryos in mammals." Reproduction 152, no. 4 (2016): R127—R141. http://dx.doi.org/10.1530/rep-16-0120.

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The oviduct is a complex and organized thin tubular structure connecting the ovary with the uterus. It is the site of final sperm capacitation, oocyte fertilization and, in most species, the first 3–4days of early embryo development. The oviductal epithelium is made up of ciliary and secretory cells responsible for the secretion of proteins and other factors which contribute to the formation of the oviductal fluid. Despite significant research, most of the pathways and oviductal factors implicated in the crosstalk between gametes/early embryo and the oviduct remain unknown. Therefore, studying

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29

Ho, Katharine, Collin A. Wolff, and Susan S. Suarez. "CatSper-null mutant spermatozoa are unable to ascend beyond the oviductal reservoir." Reproduction, Fertility and Development 21, no. 2 (2009): 345. http://dx.doi.org/10.1071/rd08183.

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Sperm hyperactivation is characterised by high-amplitude, asymmetrical flagellar bending and is required to penetrate the oocyte zona pellucida. It was proposed that hyperactivation also enables spermatozoa to reach the oocyte by assisting escape from the oviductal sperm reservoir. To test this hypothesis, the behaviour of CatSper-null mouse spermatozoa in the oviduct was compared with that of spermatozoa from heterozygotes. CatSper–/– males are infertile because their spermatozoa fail to hyperactivate, whereas spermatozoa from CatSper+/– males have normal amounts of CatSper proteins and can h

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30

Lapensée, Louise, Yves Paquette, and Gilles Bleau. "Allelic polymorphism and chromosomal localization of the human oviductin gene (MUC9)." Fertility and Sterility 68, no. 4 (1997): 702–8. http://dx.doi.org/10.1016/s0015-0282(97)00317-8.

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31

Reynolds, Lawrence P., Kacie L. McCarthy, Matthew S. Crouse, et al. "PSII-31 Effects of restricted dietary intake on protein expression of oviductal glycoprotein 1 (OVGP1) in the oviductal ampulla of beef cows." Journal of Animal Science 98, Supplement_4 (2020): 376. http://dx.doi.org/10.1093/jas/skaa278.661.

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Abstract In vitro production of embryos (IVP) results in poor pregnancy rates, with 10 to 40% of embryos transferred surviving to term. Inclusion of oviductal fluid (OF) in the culture media improves success of IVP and pregnancy rates, but factors influencing OF composition are not well investigated. Therefore, we examined the effects of restricted maternal dietary intake on expression of oviductal glycoprotein 1 (OVGP1; or oviductin), a highly conserved glycoprotein involved in fertilization and early embryo cleavage. Multiparous nonpregnant beef cows were randomly assigned to one of 2 intake

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32

Leung, A. Y., P. Y. Wong, S. E. Gabriel, J. R. Yankaskas, and R. C. Boucher. "cAMP- but not Ca(2+)-regulated Cl- conductance in the oviduct is defective in mouse model of cystic fibrosis." American Journal of Physiology-Cell Physiology 268, no. 3 (1995): C708—C712. http://dx.doi.org/10.1152/ajpcell.1995.268.3.c708.

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Defective adenosine 3',5'-cyclic monophosphate (cAMP)-mediated Cl- transport in cystic fibrosis (CF) reflects defects in the cystic fibrosis transmembrane conductance regulator (CFTR). A moderate level of CFTR mRNA expression has been found in rodent and human oviductal epithelium, but unlike other CFTR-expressing tissues, the oviduct in CF patients is apparently normal. The present study was carried out to investigate the relative magnitude of the cAMP- and intracellular Ca2+ (Cai2+)-regulated Cl- secretion in primary cultures of the oviduct from normal and CF mice generated by targeted disru

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33

Hardy, Daniel M., and Jerry L. Hedrick. "Oviductin. Purification and properties of the oviductal protease that processes the molecular weight 43,000 glycoprotein of the Xenopus laevis egg envelope." Biochemistry 31, no. 18 (1992): 4466–72. http://dx.doi.org/10.1021/bi00133a012.

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34

Roux, Emmanuelle, and Frederick W. K. Kan. "Stage-specific immunolabeling for oviductin in the secretory granules of the oviductal epithelium of the golden hamster during the estrous cycle." Anatomical Record 241, no. 3 (1995): 369–76. http://dx.doi.org/10.1002/ar.1092410311.

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35

Li, Shuai, and Wipawee Winuthayanon. "Oviduct: roles in fertilization and early embryo development." Journal of Endocrinology 232, no. 1 (2017): R1—R26. http://dx.doi.org/10.1530/joe-16-0302.

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Animal oviducts and human Fallopian tubes are a part of the female reproductive tract that hosts fertilization and pre-implantation development of the embryo. With an increasing understanding of roles of the oviduct at the cellular and molecular levels, current research signifies the importance of the oviduct on naturally conceived fertilization and pre-implantation embryo development. This review highlights the physiological conditions within the oviduct during fertilization, environmental regulation, oviductal fluid composition and its role in protecting embryos and supplying nutrients. Fina

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36

McBride, Deborah S., Chantale Boisvert, Gilles Bleau, and Frederick W. K. Kan. "Detection of Nascent and/or Mature Forms of Oviductin in the Female Reproductive Tract and Post-ovulatory Oocytes by Use of a Polyclonal Antibody Against Recombinant Hamster Oviductin." Journal of Histochemistry & Cytochemistry 52, no. 8 (2004): 1001–9. http://dx.doi.org/10.1369/jhc.3a6201.2004.

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37

Liao, S. B., J. C. Ho, F. Tang, and W. S. O. "Adrenomedullin increases ciliary beat frequency and decreases muscular contraction in the rat oviduct." REPRODUCTION 141, no. 3 (2011): 367–72. http://dx.doi.org/10.1530/rep-10-0230.

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Our laboratory previously showed that oviduct produced the greatest amount of adrenomedullin (ADM) in the rat female reproductive tract. The aim of this study is to investigate the changes in ADM levels resulting from the contact between the sperm and the oviduct and the possible roles of ADM in ciliary beating and oviductal contractility. Oviducts from Sprague–Dawley rats removed at pre- and post-ovulatory stages were cut open longitudinally and treated with ADM and/or receptor blockers before ciliary beat frequency (CBF) was measured. The effects of sperm on ADM production and CBF in the ovi

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38

Mugnier, Sylvie, Morgane Kervella, Cécile Douet, et al. "The secretions of oviduct epithelial cells increase the equine in vitro fertilization rate: are osteopontin, atrial natriuretic peptide A and oviductin involved?" Reproductive Biology and Endocrinology 7, no. 1 (2009): 129. http://dx.doi.org/10.1186/1477-7827-7-129.

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39

Akison, Lisa K., Michael J. Boden, David J. Kennaway, Darryl L. Russell, and Rebecca L. Robker. "Progesterone receptor-dependent regulation of genes in the oviducts of female mice." Physiological Genomics 46, no. 16 (2014): 583–92. http://dx.doi.org/10.1152/physiolgenomics.00044.2014.

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Oviducts play a critical role in gamete and embryo transport, as well as supporting early embryo development. Progesterone receptor (PGR) is a transcription factor highly expressed in oviductal cells, while its activating ligand, progesterone, surges to peak levels as ovulation approaches. Progesterone is known to regulate oviduct cilia beating and muscular contractions in vitro, but how PGR may mediate this in vivo is poorly understood. We used PGR null mice to identify genes potentially regulated by PGR in the oviducts during the periovulatory period. Histologically, oviducts from PGR null m

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40

Aguilar, J. J., J. Cuervo-Arango, C. Mas, M. Reyley, M. B. Rodriguez, and H. Mouguelar. "135 GLANDS IN THE OVIDUCTAL MUCOSA OF THE MARE." Reproduction, Fertility and Development 22, no. 1 (2010): 226. http://dx.doi.org/10.1071/rdv22n1ab135.

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The oviduct plays a key role in the reproductive process in mammals allowing transport, reservoir, and capacitation of sperm (Hunter RH 2008 Mol. Reprod. Dev. 75, 167-174), fertilization, and early embryo development among other events. The oviductal mucosa is organized in a vast net of folds that projects towards the lumen (Trautman A and Fiebiger J 1952 Comstock. Publ. Assoc., Ithaca, NY, USA). In a preliminary study, the presence of some glandular structures in the oviductal mucosa was noticed. Detailed histological studies have incredibly not been described in the mare. The objective of th

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41

Hachen, A., K. Jewgenow, E. Krause, and BC Braun. "Recombinant Feline Oviductin - A Powerful Tool for Functional IVF Studies in the Domestic Cat." Reproduction in Domestic Animals 47 (December 2012): 88–92. http://dx.doi.org/10.1111/rda.12030.

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42

Kimura, Hitomi, Junichiro Matsuda, Atsuo Ogura, Toshihiko Asano, and Masaharu Naiki. "Affinity binding of hamster oviductin to spermatozoa and its influence on in vitro fertilization." Molecular Reproduction and Development 39, no. 3 (1994): 322–27. http://dx.doi.org/10.1002/mrd.1080390309.

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43

Stefańska, Katarzyna, Agata Chamier-Gliszczyńska, Maurycy Jankowski, et al. "Epithelium morphogenesis and oviduct development are regulated by significant increase of expression of genes after long-term in vitro primary culture – a microarray assays." Medical Journal of Cell Biology 6, no. 4 (2018): 195–204. http://dx.doi.org/10.2478/acb-2018-0030.

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AbstractThe correct oviductal development and morphogenesis of its epithelium are crucial factors influencing female fertility. Oviduct is involved in maintaining an optimal environment for gametes and preimplantation embryo development; secretory oviductal epithelial cells (OECs) synthesize components of oviductal fluid. Oviductal epithelium also participates in sperm binding and its hyperactivation. For better understanding of the genetic bases that underlay porcine oviductal development, OECs were isolated from porcine oviducts and established long-term primary culture. A microarray approac

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Wang, L. X., S. Wang, J. Hou, Y. F. Chen, R. L. Hu, and X. R. An. "239 CANINE OOCYTES CAN BE SPONTANEOUSLY PARTHENOGENERATED AND DEVELOPED TO 2-CELL TO 8-CELL STAGE PARTHENOGENERATED EMBRYOS IN COCULTURE SYSTEM WHICH THEY WERE COCULTURED WITH OVIDUCT CELLS OR OVIDUCT EXTRACTS." Reproduction, Fertility and Development 21, no. 1 (2009): 217. http://dx.doi.org/10.1071/rdv21n1ab239.

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The objective of this study was to coculture canine oocytes with oviduct cells or oviduct extracts in modified M199 culture medium to improve the MII rate. The canine oocytes were collected from the local slaughterhouse and were cultured in three culture systems while in the same culture medium. In culture system A, canine oocytes were cocultured with ‘small-round’ oviduct cells and ‘big-round’ oviductal cells which based on cell volume and morphology for 96 h. In culture system B, canine oocytes were cultured with in the modified M199 medium with 10% canine follicle fluid (in the CEF group) o

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Zerani, M., C. Boiti, C. Dall’Aglio, et al. "Leptin receptor expression and in vitro leptin actions on prostaglandin release and nitric oxide synthase activity in the rabbit oviduct." Journal of Endocrinology 185, no. 2 (2005): 319–25. http://dx.doi.org/10.1677/joe.1.05983.

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In this study, we have examined the presence and the distribution of receptors for leptin (Ob-R) in the oviduct of rabbits, and the effects of leptin on the release of prostaglandin (PG) F2α and PGE2 and on the activity of nitric oxide (NO) synthase (NOS) by oviducts cultured in vitro. Rabbits were killed during the follicular phase and the oviducts were incubated in vitro with leptin, PGF2α, PGE2, NO donor and inhibitors of NOS and cyclo-oxigenase (COX). Using immunohistochemistry, Ob-R-like positive reaction was observed only in the cytoplasm of secretory cells, having stronger intensity in

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Paliwal, A., B. Malaviya, and VP Kamboj. "Oviductal fluid protein patterns in the rhesus monkey (Macaca mulatta) during the menstrual cycle." Reproduction, Fertility and Development 4, no. 2 (1992): 249. http://dx.doi.org/10.1071/rd9920249.

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Oviducts were obtained from monkeys on Days 8, 14, 19 and 25 of the menstrual cycle and changes in the pattern of luminal fluid proteins were examined by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). Densitometric analysis after periodic acid Schiff's reagent (PAS) and coomassie blue staining of the gels revealed 85 and 95 kDa proteins only up to Day 14 whereas a 130 kDa glycoprotein persisted up to Day 19 and reached a nadir at mid-menstrual cycle (Day 14). The absence of the 130 kDa glycoprotein in the serum and its presence in cytosolic preparations up to Day 19 sugg

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Kimura, H., J. Matsuda, A. Ogura, T. Asano, and M. Naiki. "S8.22 The binding of hamster oviductin to spermatozoa and its inhibitory effect toin vitro fertilization." Glycoconjugate Journal 10, no. 4 (1993): 272–73. http://dx.doi.org/10.1007/bf01209964.

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Ayad, V. J., S. A. McGoff, and D. C. Wathes. "Oxytocin receptors in the oviduct during the oestrous cycle of the ewe." Journal of Endocrinology 124, no. 3 (1990): 353–59. http://dx.doi.org/10.1677/joe.0.1240353.

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ABSTRACT The presence of oxytocin receptors in ovine oviduct has been investigated. High-affinity binding sites for [3H]oxytocin were detected in crude membrane fractions prepared from the oviducts of ewes killed during the oestrous period. The dissociation constant calculated for these sites in competition studies was 1·7 nmol/l. Similar dissociation constants were calculated for [Arg8]-vasopressin and the oxytocin-specific agonists [Gly7]-oxytocin and [Thr4, Gly7]-oxytocin, indicating that these sites represent oxytocin receptors. At least one additional site of lower affinity and undetermin

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Okada, A., Y. Ohta, SL Brody, et al. "Role of foxj1 and estrogen receptor alpha in ciliated epithelial cell differentiation of the neonatal oviduct." Journal of Molecular Endocrinology 32, no. 3 (2004): 615–25. http://dx.doi.org/10.1677/jme.0.0320615.

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Estrogen regulates proliferation and differentiation of epithelial cells in the mammalian oviduct, but pathways for cell-specific differentiation are not well understood. In the epithelial cells of the developing rat oviduct, we found estrogen receptor (ER) alpha is expressed at birth and persists in all cells through neonatal day (ND) 7 when ciliated cells appear. To determine a specific function of ER and foxj1, a transcription factor known to have fundamental roles in ciliogenesis in the lung, in differentiation of the ciliated epithelial cells, we treated newborn rats from ND 0 to 5 with e

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Hiyoshi, Masateru, Kazufumi Takamune, Koichi Mita, Hideo Kubo, Yasusi Sugimoto, and Chiaki Katagiri. "Oviductin, the Oviductal Protease That Mediates Gamete Interaction by Affecting the Vitelline Coat in Bufo japonicus: Its Molecular Cloning and Analyses of Expression and Posttranslational Activation." Developmental Biology 243, no. 1 (2002): 176–84. http://dx.doi.org/10.1006/dbio.2001.0558.

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