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Differentiation of Mouse Primordial Germ Cells into Functional Oocytes In Vitro

Various complex molecular events in oogenesis cannot be observed in vivo. As a bioengineering technique for female reproductive tissues, in vitro culture systems for female germ cells have been used to analyze oogenesis and preserve germ cells for over 20 years. Recently, we have established a new m...

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Detalles Bibliográficos
Autores principales: Morohaku, Kanako, Hirao, Yuji, Obata, Yayoi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489615/
https://www.ncbi.nlm.nih.gov/pubmed/28243826
http://dx.doi.org/10.1007/s10439-017-1815-7
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author Morohaku, Kanako
Hirao, Yuji
Obata, Yayoi
author_facet Morohaku, Kanako
Hirao, Yuji
Obata, Yayoi
author_sort Morohaku, Kanako
collection PubMed
description Various complex molecular events in oogenesis cannot be observed in vivo. As a bioengineering technique for female reproductive tissues, in vitro culture systems for female germ cells have been used to analyze oogenesis and preserve germ cells for over 20 years. Recently, we have established a new methodological approach for the culture of primordial germ cells (PGCs) and successfully obtained offspring. Our PGC culture system will be useful to clarify unresolved mechanisms of fertility and sterility from the beginning of mammalian oogenesis, before meiosis. This review summarizes the history of culture methods for mammalian germ cells, our current in vitro system, and future prospects for the culture of germ cells.
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spelling pubmed-54896152017-07-03 Differentiation of Mouse Primordial Germ Cells into Functional Oocytes In Vitro Morohaku, Kanako Hirao, Yuji Obata, Yayoi Ann Biomed Eng Reproductive Tissue Engineering Various complex molecular events in oogenesis cannot be observed in vivo. As a bioengineering technique for female reproductive tissues, in vitro culture systems for female germ cells have been used to analyze oogenesis and preserve germ cells for over 20 years. Recently, we have established a new methodological approach for the culture of primordial germ cells (PGCs) and successfully obtained offspring. Our PGC culture system will be useful to clarify unresolved mechanisms of fertility and sterility from the beginning of mammalian oogenesis, before meiosis. This review summarizes the history of culture methods for mammalian germ cells, our current in vitro system, and future prospects for the culture of germ cells. Springer US 2017-02-27 2017 /pmc/articles/PMC5489615/ /pubmed/28243826 http://dx.doi.org/10.1007/s10439-017-1815-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Reproductive Tissue Engineering
Morohaku, Kanako
Hirao, Yuji
Obata, Yayoi
Differentiation of Mouse Primordial Germ Cells into Functional Oocytes In Vitro
title Differentiation of Mouse Primordial Germ Cells into Functional Oocytes In Vitro
title_full Differentiation of Mouse Primordial Germ Cells into Functional Oocytes In Vitro
title_fullStr Differentiation of Mouse Primordial Germ Cells into Functional Oocytes In Vitro
title_full_unstemmed Differentiation of Mouse Primordial Germ Cells into Functional Oocytes In Vitro
title_short Differentiation of Mouse Primordial Germ Cells into Functional Oocytes In Vitro
title_sort differentiation of mouse primordial germ cells into functional oocytes in vitro
topic Reproductive Tissue Engineering
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5489615/
https://www.ncbi.nlm.nih.gov/pubmed/28243826
http://dx.doi.org/10.1007/s10439-017-1815-7
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AT obatayayoi differentiationofmouseprimordialgermcellsintofunctionaloocytesinvitro