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Journal articles on the topic 'Chick embryo - Embryology'

Author: Grafiati

Published: 4 June 2021

Last updated: 11 February 2022

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1

Mishrikoti, Harsh P., and Umesh К. Kulkarni. "An early chick embryo as learning model for study of embryology." National Journal of Clinical Anatomy 7, no. 04 (October 2018): 177–82. http://dx.doi.org/10.1055/s-0040-1701733.

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Abstract Background: In medical education, learning happens by variety of perceptions. In basic science Anatomy, visualization of real structures gives rich learning experience. This type seems deficient in human embryology, that too in the early phases. Aim: With the basic concept of'ontogeny repeats phylogeny', for the enrichment of learning early embryology, chick embryos have been used. Materials and methods: 30 commercially available chicken eggs and 30 Gallus domesticus [country chicken] eggs collected from nearby villages were hatched for embryos to whole mount, fix and stain. Results: Successful hatching rates were more in favour of Gallus domesticus eggs [76%] compared to others [26%] Conclusion: This experiment guides the easiest and simplest possible ways to successfully establish the learning module for early embryology in departmental setup using Gallus domesticus eggs. Observation of brain swellings, heart swelling optic vesicle, nasal pit, pharyngeal clefts, neural tube, somites and limb buds, vitelline vessels provide valuable learning experience by direct interaction with the real environment. This bridges the gap of seeing what is not usually observed and strengthens educational embryology

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2

Kulkarni, UmeshK, and HarshP Mishrikoti. "An early chick embryo as learning model for study of embryology." National Journal of Clinical Anatomy 7, no. 4 (2018): 177. http://dx.doi.org/10.4103/2277-4025.294769.

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3

Hollyday, Margaret, Jill A. McMahon, and Andrew P. McMahon. "Wnt expression patterns in chick embryo nervous system." Mechanisms of Development 52, no. 1 (July 1995): 9–25. http://dx.doi.org/10.1016/0925-4773(95)00385-e.

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4

Pourquié, Olivier. "The chick embryo: a leading model in somitogenesis studies." Mechanisms of Development 121, no. 9 (September 2004): 1069–79. http://dx.doi.org/10.1016/j.mod.2004.05.002.

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5

Bertocchini, Federica, and Claudio Stern. "04-P002 Axis determination in the early chick embryo." Mechanisms of Development 126 (August 2009): S107. http://dx.doi.org/10.1016/j.mod.2009.06.187.

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6

Griffith, C. M., and E. J. Sanders. "Differentiation of the chick embryo floor plate." Anatomy and Embryology 184, no. 2 (1991): 159–69. http://dx.doi.org/10.1007/bf00942747.

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7

Ghaskadbi, Surendra. "Leela Mulherkar and the teaching of developmental biology." International Journal of Developmental Biology 64, no. 1-2-3 (2020): 41–44. http://dx.doi.org/10.1387/ijdb.200147sg.

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The formal teaching of developmental biology in India began in the late nineteen-fifties at the Department of Zoology of the University of Poona. This was due to the efforts of Leela Mulherkar, who on her return from C.H. Waddington’s laboratory in Edinburgh, took up the teaching of embryology at the Master’s level. Mulherkar began using locally available material to teach how animals develop. They included the embryos of chicken, frog, garden lizard and molluscs, as well as organisms such as hydra and sponges. Her teaching was supported by an active research laboratory that used all these systems to address a variety of questions in embryology and teratology. She used chick embryo explants cultured in vitro extensively in her work. Teaching and research in embryology at the master’s and doctoral levels at Poona University subsequently led, in 1977, to the establishment of the Indian Society of Developmental Biologists (InSDB), which is among the most active scientific societies in India.

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8

Lee, Hyung Chul, Hui-Chun Lu, Mark Turmaine, Nidia M. M. Oliveira, Youwen Yang, Irene De Almeida, and Claudio D. Stern. "Molecular anatomy of the pre-primitive-streak chick embryo." Open Biology 10, no. 2 (February 2020): 190299. http://dx.doi.org/10.1098/rsob.190299.

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The early stages of development of the chick embryo, leading to primitive streak formation (the start of gastrulation), have received renewed attention recently, especially for studies of the mechanisms of large-scale cell movements and those that position the primitive streak in the radial blastodisc. Over the long history of chick embryology, the terminology used to define different regions has been changing, making it difficult to relate studies to each other. To resolve this objectively requires precise definitions of the regions based on anatomical and functional criteria, along with a systematic molecular map that can be compared directly to the functional anatomy. Here, we undertake these tasks. We describe the characteristic cell morphologies (using scanning electron microscopy and immunocytochemistry for cell polarity markers) in different regions and at successive stages. RNAseq was performed for 12 regions of the blastodisc, from which a set of putative regional markers was selected. These were studied in detail by in situ hybridization. Together this provides a comprehensive resource allowing the community to define the regions unambiguously and objectively. In addition to helping with future experimental design and interpretation, this resource will also be useful for evolutionary comparisons between different vertebrate species.

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9

Schubert, Frank R., Roy C. Mootoosamy, Esther H. Walters, Anthony Graham, Loretta Tumiotto, Andrea E. Münsterberg, Andrew Lumsden, and Susanne Dietrich. "Wnt6 marks sites of epithelial transformations in the chick embryo." Mechanisms of Development 114, no. 1-2 (June 2002): 143–48. http://dx.doi.org/10.1016/s0925-4773(02)00039-4.

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10

Ribatti, Domenico. "The chick embryo chorioallantoic membrane (CAM). A multifaceted experimental model." Mechanisms of Development 141 (August 2016): 70–77. http://dx.doi.org/10.1016/j.mod.2016.05.003.

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11

Montecorboli, Umberto, Tiziana Annese, Christian Marinaccio, and Domenico Ribatti. "Angiogenesis and hyperbaric oxygen in the chick embryo chorioallantoic membrane." International Journal of Developmental Biology 59, no. 10-11-12 (2015): 461–64. http://dx.doi.org/10.1387/ijdb.150280dr.

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12

Modak, Sohan Prabhakar. "Cell population growth regulates dorsalization and caudalization during chick morphogenesis and programmed cell death in lens fibres." International Journal of Developmental Biology 64, no. 1-2-3 (2020): 45–57. http://dx.doi.org/10.1387/ijdb.190270sm.

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The chick embryo ectoblast was examined for a possible relationship between the state of neural competence and cell population growth. It was found that although ectoblast cells with doubling times ranging between 5 to 20 h exhibit neural competence, the extent of neutralization induced by the Hensen’s node depends on the duration of the cell cycle; the longer the doubling time of the competent ectoblast, the stronger the induction and the greater the induced neural tissue. Neural induction in the competent ectoblast occurs in at least two steps: the first lasts for 1-2 h of direct contact with the inducing Hensen’s node graft; a contact for another 2 h with even a non-inducing post-nodal fragment is essential to consolidate neutralization. Hensen’s node graft induces mitotic activity in the competent ectoblast in contact. Teratogens which inhibit cell population growth, development and blastoderm expansion in chick embryo gastrula cause concomitant caudalization of the embryonic axis. We confirm Yamada’s hypothesis that dorsalization is under positive mitogenic control, whereas caudalization is controlled by a negative cell cycle regulation. Reverse transcripts of chick gastrula mRNA were cloned in pBR322. Colony hybridization with cDNA made against chicken yolk RNA showed positive clones. Thus chicken yolk contains maternal mRNAs. cDNA made against mRNA extracted from stage 10 foreheads was hybridized with RNA from stage 1 to 13 embryos, 19 day lens and egg yolk. The hybridization signal, which was low between stages 1 to 7, increased between stages 10-13 and decreased thereafter. Forehead cDNA also hybridized to yolk RNA. Thus, maternal RNA sequences are present in the early chick embryo. During lens development, epithelial cells retain proliferative activity and their progeny reaching a stationary phase join the fibre area and contribute to the growth of fibre cells. The rate of transfer from epithelium to fibre regulates the rate of programmed cell death of the non-dividing differentiated lens fibre cells.

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13

Gupta, Sandeep, Niveda Udaykumar, and Jonaki Sen. "Forebrain roof plate morphogenesis and hippocampus development in the chick embryo." International Journal of Developmental Biology 64, no. 1-2-3 (2020): 247–57. http://dx.doi.org/10.1387/ijdb.190143js.

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The forebrain roof plate undergoes dramatic morphogenetic changes to invaginate, and this leads to formation of the two cerebral hemispheres. While many genetic factors are known to regulate this process, the mechanism of forebrain roof plate invagination remains unknown. In a recent study we have identified retinoic acid as a signal from the dorsal mesenchyme that regulates the invagination of the roof plate. This has brought into focus the importance of the interaction between the dorsal mesenchyme and the underlying roof plate. One of the structures derived from the dorso-medial forebrain after roof plate invagination is the hippocampus. While the functions of the hippocampus are conserved between birds and mammals, there are distinct structural differences. We have studied hippocampus development in the chick embryo and uncovered several similarities and differences between the process in mammals and birds. This study has also lent support to one of the prevalent models of structural homology between the avian and mammalian hippocampus. In this review, we have underscored the importance of the chick embryo as a model for studying forebrain roof plate morphogenesis and hippocampus development.

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14

Raya, Angel, and Juan Carlos Izpisua Belmonte. "Unveiling the establishment of left–right asymmetry in the chick embryo." Mechanisms of Development 121, no. 9 (September 2004): 1043–54. http://dx.doi.org/10.1016/j.mod.2004.05.005.

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15

Forsyth, C. S., A. A. Frank, B. J. Watrous, and A. A. Bohn. "Effect of coniine on the developing chick embryo." Teratology 49, no. 4 (April 1994): 306–10. http://dx.doi.org/10.1002/tera.1420490410.

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16

Yusuf, Faisal, Rizwan Rehimi, Fangping Dai, and Beate Brand-Saberi. "Expression of chemokine receptor CXCR4 during chick embryo development." Anatomy and Embryology 210, no. 1 (July 27, 2005): 35–41. http://dx.doi.org/10.1007/s00429-005-0013-9.

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17

Kang, Xing, and Weerapong Prasongchean. "Effects of alcohol on the development of choroid plexus in chick embryo." Mechanisms of Development 145 (July 2017): S127. http://dx.doi.org/10.1016/j.mod.2017.04.348.

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18

Zagris, Nikolas, Albert E. Chung, and Vassilis Stavridis. "Entactin and laminin gamma1-chain gene expression in the early chick embryo." International Journal of Developmental Biology 49, no. 1 (2005): 65–70. http://dx.doi.org/10.1387/ijdb.041812nz.

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19

Gibson, Anna, Neil Robinson, Andrea Streit, Guojun Sheng, and Claudio D. Stern. "Regulation of programmed cell death during neural induction in the chick embryo." International Journal of Developmental Biology 55, no. 1 (2011): 33–43. http://dx.doi.org/10.1387/ijdb.103233sg.

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20

Afman, L. A., H. J. Blom, N. M. J. Van Der Put, and H. W. M. Van Straaten. "Homocysteine interference in neurulation: A chick embryo model." Birth Defects Research Part A: Clinical and Molecular Teratology 67, no. 6 (June 2003): 421–28. http://dx.doi.org/10.1002/bdra.10040.

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21

Navascu�s, J., G. Mart�n-Partido, I. S. Alvarez, L. Rodr�guez-Gallardo, and V. Garc�a-Mart�nez. "Glioblast migration in the optic stalk of the chick embryo." Anatomy and Embryology 176, no. 1 (April 1987): 79–85. http://dx.doi.org/10.1007/bf00309755.

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22

Melian, A. Pe�a, J. Puerta Fonolla, and P. Gil Loyzaga. "The ontogeny of the cerebellar fissures in the chick embryo." Anatomy and Embryology 175, no. 1 (November 1986): 119–28. http://dx.doi.org/10.1007/bf00315462.

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23

Fang, Tzann-Tarn, Harold J. Bruyere, Steve A. Kargas, Toshio Nishikawa, Yasuo Takagi, and Enid F. Gilbert. "Ethyl alcohol-induced cardiovascular malformations in the chick embryo." Teratology 35, no. 1 (February 1987): 95–103. http://dx.doi.org/10.1002/tera.1420350113.

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24

Nishibatake, Makoto, Steve A. Kargas, Harold J. Bruyere, and Enid F. Gilbert. "Cardiovascular malformations induced by bromodeoxyuridine in the chick embryo." Teratology 36, no. 1 (August 1987): 125–32. http://dx.doi.org/10.1002/tera.1420360116.

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25

Schoenwolf, Gary C. "Contributions of the chick embryo and experimental embryology to understanding the cellular mechanisms of neurulation." International Journal of Developmental Biology 62, no. 1-2-3 (2018): 49–55. http://dx.doi.org/10.1387/ijdb.170288gs.

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26

Jayaraj, Perumal, Vani Srinivasan, Sejal Sharma, Deepanjan Banerjee, Nabanita Ghosh, Abhimanyu Singh, Mehak Madan, and Nimita Kant. "A cost-effective set-up to demonstrate embryonic limb development in Aseel (Gallus gallus domesticus)." South Asian Journal of Experimental Biology 11, no. 3 (May 24, 2021): 260–65. http://dx.doi.org/10.38150/sajeb.11(3).p260-265.

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Limb development during embryogenesis is a classical model used to study pattern formation. Experiments with biological model systems currently re-quire expensive equipment to maintain optimal conditions, an impractical option for low-scale studies. Currently popular ex-vivo methods lead to stunted embryonic limb development, a high infection and fatality rate. As an alternative, the presented paper uses a novel, cost-effective set up to study the developing chick embryo as a biological model in order to visualize Chondrogenesis alongwith formation of ossification centers and apoptotic events occurring in the limb bud of the developing embryo.This cup-in-cup model constructed using polystyrene cups is instrumental in observing the developing embryos and correlating them to Hamilton-Hamburger (HH) de-velopmental stages without exposing them to the outside environment and approaching a near perfect embryo survival rate. Anatomical events during skeleton development such as chondrogenesis, osteogenesis, and apoptosis are studied using Alcian Blue, Alizarin Red and Nile Blue Sulphate staining protocols revealing successful formation and progression of ossification cen-ters and apoptotic regions in the limb bud. The chick embryo system is an excellent model that aids in understanding osteogenesis at both basic and clinical science level and enhance our knowledge about embryological devel-opment. The cup-in-cup system presented in this study proves to be a realis-tic addition to the subject of embryology and an ideal, sustainable experi-mental medium for low-scale research studies.

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27

Püschel, Bernd, and Jörg Männer. "Use of the Coelomic Grafting Technique for Prolonged ex utero Cultivation of Late Preprimitive Streak-Stage Rabbit Embryos." Cells Tissues Organs 202, no. 5-6 (2016): 329–42. http://dx.doi.org/10.1159/000446820.

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Due to its morphological similarity with the early human embryo, the pregastrulation-stage rabbit may represent an appropriate mammalian model for studying processes involved in early human development. The usability of mammalian embryos for experimental studies depends on the availability of whole embryo culture methods facilitating prolonged ex utero development. While currently used culture methods yield high success rates for embryos from primitive streak stages onward, the success rate of extended cultivation of preprimitive streak-stage mammalian embryos is low for all previously established methods and for all studied species. This limits the usability of preprimitive streak-stage rabbit embryos in experimental embryology. We have tested whether the extraembryonic coelom of 4-day-old chick embryos may be used for prolonged ex utero culture of preprimitive streak-stage rabbit embryos (stage 2, 6.2 days post coitum). We found that, within this environment, stage 2 rabbit blastocysts can be cultured at decreasing success rates (55% after 1 day, 35% after 2 days, 15% after 3 days) up to a maximum of 72 h. Grafted blastocysts can continue development from the onset of gastrulation to early organogenesis and thereby form all structures characterizing age-matched controls (e.g. neural tube, somites, beating heart). Compared to normal controls, successfully cultured embryos developed at a slower rate and finally showed some structural and gross morphological anomalies. The method presented here was originally developed for whole embryo culture of mouse embryos by Gluecksohn-Schoenheimer in 1941. It is a simple and inexpensive method that may represent a useful extension to presently available ex utero culture systems for rabbit embryos.

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28

Drews, Ulrich, Cecilia Ebensperger, and Ulrich Wolf. "An in vitro model of gonad differentiation in the chick embryo." Anatomy and Embryology 178, no. 6 (September 1988): 529–36. http://dx.doi.org/10.1007/bf00305040.

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29

Flamme, Ingo. "Edge cell migration in the extraembryonic mesoderm of the chick embryo." Anatomy and Embryology 176, no. 4 (September 1987): 477–91. http://dx.doi.org/10.1007/bf00310088.

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30

Vaccaro, R., E. Parisi Salvi, and T. Renda. "Early development of chick embryo respiratory nervous system: an immunohistochemical study." Anatomy and Embryology 211, no. 5 (April 22, 2006): 345–54. http://dx.doi.org/10.1007/s00429-006-0089-x.

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31

Kärner, Martin, Dagni Krinka, Kärt Padari, Jüri Kärner, and R. Raid. "Dorsoventral compartmentalization of mesoderm in heart-forming area of chick embryo." Anatomy and Embryology 201, no. 6 (May 29, 2000): 501–7. http://dx.doi.org/10.1007/s004290050337.

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32

Bertossi, Mirella, Luisa Roncali, Lucia Mancini, Domenico Ribatti, and Beatrice Nico. "Process of differentiation of cerebellar Purkinje neurons in the chick embryo." Anatomy and Embryology 175, no. 1 (November 1986): 25–34. http://dx.doi.org/10.1007/bf00315453.

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33

Flamme, Ingo. "Is extraembryonic angiogenesis in the chick embryo controlled by the endoderm?" Anatomy and Embryology 180, no. 3 (August 1989): 259–72. http://dx.doi.org/10.1007/bf00315884.

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34

Gabella, Giorgio. "Development of smooth muscle: ultrastructural study of the chick embryo gizzard." Anatomy and Embryology 180, no. 3 (August 1989): 213–26. http://dx.doi.org/10.1007/bf00315880.

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35

Mills, C. L., and Ruth Bellairs. "Mitosis and cell death in the tail of the chick embryo." Anatomy and Embryology 180, no. 3 (August 1989): 301–8. http://dx.doi.org/10.1007/bf00315888.

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36

Jaffee, Oscar C., and Andrew L. Jaffee. "Ectopia cordis in the chick embryo heart: An experimental study." Teratology 41, no. 6 (June 1990): 737–42. http://dx.doi.org/10.1002/tera.1420410611.

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37

Katsumoto, Keiichi, Kimiko Fukuda, Wataru Kimura, Kenji Shimamura, Sadao Yasugi, and Shoen Kume. "Origin of pancreatic precursors in the chick embryo and the mechanism of endoderm regionalization." Mechanisms of Development 126, no. 7 (July 2009): 539–51. http://dx.doi.org/10.1016/j.mod.2009.03.006.

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38

Teixeira, Vera, Natacha Arede, Gabriel Martins, Barbara Fekete, Nuno Moreno, and Ana Teresa Tavares. "03-P065 Identification and molecular characterisation of the hemangioblast in the early chick embryo." Mechanisms of Development 126 (August 2009): S85—S86. http://dx.doi.org/10.1016/j.mod.2009.06.118.

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39

Kayam, Galya, and Dalit Sela-Donenfeld. "13-P131 Pax6 is involved in the early hindbrain patterning in the chick embryo." Mechanisms of Development 126 (August 2009): S234. http://dx.doi.org/10.1016/j.mod.2009.06.604.

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40

Md, Makoto Nakazawa, Takashi Ohno, Sachiko Miyagawa, and Atsuyoshi Takao. "Hemodynamic effects of acetylcholine in the chick embryo and differences from those in the rat embryo." Teratology 39, no. 6 (June 1989): 555–61. http://dx.doi.org/10.1002/tera.1420390606.

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41

Hedge, Thomas A., and Ivor Mason. "Expression of Shisa2, a modulator of both Wnt and Fgf signaling, in the chick embryo." International Journal of Developmental Biology 52, no. 1 (2008): 81–85. http://dx.doi.org/10.1387/ijdb.072355th.

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42

Osorio, Liliana, Marie-Aimee Teillet, Isabel Palmeirim, and Martin Catala. "Neural crest ontogeny during secondary neurulation: a gene expression pattern study in the chick embryo." International Journal of Developmental Biology 53, no. 4 (2009): 641–48. http://dx.doi.org/10.1387/ijdb.072517lo.

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43

Alexander, Peter G., and Rocky S. Tuan. "Carbon monoxide-induced axial skeletal dysmorphogenesis in the chick embryo." Birth Defects Research Part A: Clinical and Molecular Teratology 67, no. 4 (April 2003): 219–30. http://dx.doi.org/10.1002/bdra.10041.

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44

Spence, Hilda Adele, and Richard J. O'Callaghan. "Induction of chick embryo feather malformations by an influenza C virus." Teratology 32, no. 1 (August 1985): 57–64. http://dx.doi.org/10.1002/tera.1420320109.

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45

Narbaitz, Roberto, Irma Marino, and Kiriti Sarkar. "Lead-induced early lesions in the brain of the chick embryo." Teratology 32, no. 3 (December 1985): 389–96. http://dx.doi.org/10.1002/tera.1420320309.

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46

Sanders, E. J., E. Cheung, and E. Mahmud. "Ethanol treatment inhibits mesoderm cell spreading in the gastrulating chick embryo." Teratology 36, no. 2 (October 1987): 209–16. http://dx.doi.org/10.1002/tera.1420360208.

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47

Sanders, E. J., and E. Cheung. "Ethanol treatment induces a delayed segmentation anomaly in the chick embryo." Teratology 41, no. 3 (March 1990): 289–97. http://dx.doi.org/10.1002/tera.1420410306.

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48

Lenselink, Daniel R., John E. Midtling, and Gary L. Kolesari. "Teratogenesis associated with oxydemeton-methyl in the stage 12 chick embryo." Teratology 48, no. 3 (September 1993): 207–11. http://dx.doi.org/10.1002/tera.1420480304.

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49

Akai, Jun, and Kate Storey. "Expression of γ-adducin is associated with regions of morphogenetic cell movement in the chick embryo." Mechanisms of Development 119 (December 2002): S191—S195. http://dx.doi.org/10.1016/s0925-4773(03)00115-1.

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50

Patwardhan, Vidya, Madhavi Gokhale, and Surendra Ghaskadbi. "Acceleration of early chick embryo morphogenesis by insulin is associated with altered expression of embryonic genes." International Journal of Developmental Biology 48, no. 4 (2004): 319–26. http://dx.doi.org/10.1387/ijdb.041844vp.

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