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Derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat

Germ cells are responsible for the propagation of live animals from generation to generation, but to surprise, a steep increase in infertile problems among livestock poses great threat for economic development of human race. An alternative and robust approach is essential to combat these ailments. H...

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Autores principales: Malik, Hruda Nanda, Singhal, Dinesh Kumar, Saini, Sikander, Malakar, Dhruba
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308273/
https://www.ncbi.nlm.nih.gov/pubmed/32572061
http://dx.doi.org/10.1038/s41598-020-66609-2
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author Malik, Hruda Nanda
Singhal, Dinesh Kumar
Saini, Sikander
Malakar, Dhruba
author_facet Malik, Hruda Nanda
Singhal, Dinesh Kumar
Saini, Sikander
Malakar, Dhruba
author_sort Malik, Hruda Nanda
collection PubMed
description Germ cells are responsible for the propagation of live animals from generation to generation, but to surprise, a steep increase in infertile problems among livestock poses great threat for economic development of human race. An alternative and robust approach is essential to combat these ailments. Here, we demonstrate that goat putative embryonic stem cells (ESCs) were successfully in vitro differentiated into primordial germ cells and oocyte-like cells using bone morphogenetic protein-4 (BMP-4) and trans-retinoic acid (RA). Oocyte-like cells having distinct zonapellucida recruited adjacent somatic cells in differentiating culture to form cumulus-oocyte complexes (COCs). The putative COCs were found to express the zonapellucida specific (ZP1 and ZP2) and oocyte-specific markers. Primordial germ cell-specific markers VASA, DAZL, STELLA, and PUM1 were detected at protein and mRNA level. In addition to that, the surface architecture of these putative COCs was thoroughly visualized by the scanning electron microscope. The putative COCs were further parthenogenetically activated to develop into healthy morula, blastocysts and hatched blastocyst stage like embryos. Our findings may contribute to the fundamental understanding of mammalian germ cell biology and may provide clinical insights regarding infertility ailments.
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spelling pubmed-73082732020-06-23 Derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat Malik, Hruda Nanda Singhal, Dinesh Kumar Saini, Sikander Malakar, Dhruba Sci Rep Article Germ cells are responsible for the propagation of live animals from generation to generation, but to surprise, a steep increase in infertile problems among livestock poses great threat for economic development of human race. An alternative and robust approach is essential to combat these ailments. Here, we demonstrate that goat putative embryonic stem cells (ESCs) were successfully in vitro differentiated into primordial germ cells and oocyte-like cells using bone morphogenetic protein-4 (BMP-4) and trans-retinoic acid (RA). Oocyte-like cells having distinct zonapellucida recruited adjacent somatic cells in differentiating culture to form cumulus-oocyte complexes (COCs). The putative COCs were found to express the zonapellucida specific (ZP1 and ZP2) and oocyte-specific markers. Primordial germ cell-specific markers VASA, DAZL, STELLA, and PUM1 were detected at protein and mRNA level. In addition to that, the surface architecture of these putative COCs was thoroughly visualized by the scanning electron microscope. The putative COCs were further parthenogenetically activated to develop into healthy morula, blastocysts and hatched blastocyst stage like embryos. Our findings may contribute to the fundamental understanding of mammalian germ cell biology and may provide clinical insights regarding infertility ailments. Nature Publishing Group UK 2020-06-22 /pmc/articles/PMC7308273/ /pubmed/32572061 http://dx.doi.org/10.1038/s41598-020-66609-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Malik, Hruda Nanda
Singhal, Dinesh Kumar
Saini, Sikander
Malakar, Dhruba
Derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat
title Derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat
title_full Derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat
title_fullStr Derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat
title_full_unstemmed Derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat
title_short Derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat
title_sort derivation of oocyte-like cells from putative embryonic stem cells and parthenogenetically activated into blastocysts in goat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308273/
https://www.ncbi.nlm.nih.gov/pubmed/32572061
http://dx.doi.org/10.1038/s41598-020-66609-2
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