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Human GV oocytes generated by mitotically active germ cells obtained from follicular aspirates
Human female germline stem cells (FGSCs) have opened new opportunities for understanding human oogenesis, delaying menopause, treating infertility, and providing a new strategy for preserving fertility. However, the shortage of adult human ovaries tissues available impedes their future investigation...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928061/ https://www.ncbi.nlm.nih.gov/pubmed/27357640 http://dx.doi.org/10.1038/srep28218 |
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author | Ding, Xinbao Liu, Guishu Xu, Bo Wu, Changqing Hui, Ning Ni, Xin Wang, Jian Du, Meirong Teng, Xiaoming Wu, Ji |
author_facet | Ding, Xinbao Liu, Guishu Xu, Bo Wu, Changqing Hui, Ning Ni, Xin Wang, Jian Du, Meirong Teng, Xiaoming Wu, Ji |
author_sort | Ding, Xinbao |
collection | PubMed |
description | Human female germline stem cells (FGSCs) have opened new opportunities for understanding human oogenesis, delaying menopause, treating infertility, and providing a new strategy for preserving fertility. However, the shortage of adult human ovaries tissues available impedes their future investigations and clinical applications. Here, we have established FGSC lines from scarce ovarian cortical tissues that exist in follicular aspirates (faFGSCs), which are produced and discarded in in vitro fertilization centers worldwide. The faFGSCs have characteristics of germline stem cells involved in the gene expression profile, growth characteristics, and a normal karyotype consistent with that of FGSCs obtained from ovarian cortexes surgically removed from patients (srFGSCs). Furthermore, faFGSCs have developmental potentials including spontaneous differentiation into oocytes under feeder-free conditions, communicating with granulosa cells by gap junctions and paracrine factors, entering meiosis after RA induction, as well as forming follicles after injection into human ovarian cortical tissues xenografted into adult immunodeficient female mice. Lastly, we developed a strategy guiding FGSCs differentiated into germinal vesicle (GV) stage oocytes in vitro and revealed their developmental mechanisms. Our study not only provides a new approach to obtain human FGSCs for medical treatment, but also opens several avenues to investigate human oogenesis in vitro. |
format | Online Article Text |
id | pubmed-4928061 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49280612016-07-01 Human GV oocytes generated by mitotically active germ cells obtained from follicular aspirates Ding, Xinbao Liu, Guishu Xu, Bo Wu, Changqing Hui, Ning Ni, Xin Wang, Jian Du, Meirong Teng, Xiaoming Wu, Ji Sci Rep Article Human female germline stem cells (FGSCs) have opened new opportunities for understanding human oogenesis, delaying menopause, treating infertility, and providing a new strategy for preserving fertility. However, the shortage of adult human ovaries tissues available impedes their future investigations and clinical applications. Here, we have established FGSC lines from scarce ovarian cortical tissues that exist in follicular aspirates (faFGSCs), which are produced and discarded in in vitro fertilization centers worldwide. The faFGSCs have characteristics of germline stem cells involved in the gene expression profile, growth characteristics, and a normal karyotype consistent with that of FGSCs obtained from ovarian cortexes surgically removed from patients (srFGSCs). Furthermore, faFGSCs have developmental potentials including spontaneous differentiation into oocytes under feeder-free conditions, communicating with granulosa cells by gap junctions and paracrine factors, entering meiosis after RA induction, as well as forming follicles after injection into human ovarian cortical tissues xenografted into adult immunodeficient female mice. Lastly, we developed a strategy guiding FGSCs differentiated into germinal vesicle (GV) stage oocytes in vitro and revealed their developmental mechanisms. Our study not only provides a new approach to obtain human FGSCs for medical treatment, but also opens several avenues to investigate human oogenesis in vitro. Nature Publishing Group 2016-06-30 /pmc/articles/PMC4928061/ /pubmed/27357640 http://dx.doi.org/10.1038/srep28218 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ding, Xinbao Liu, Guishu Xu, Bo Wu, Changqing Hui, Ning Ni, Xin Wang, Jian Du, Meirong Teng, Xiaoming Wu, Ji Human GV oocytes generated by mitotically active germ cells obtained from follicular aspirates |
title | Human GV oocytes generated by mitotically active germ cells obtained from follicular aspirates |
title_full | Human GV oocytes generated by mitotically active germ cells obtained from follicular aspirates |
title_fullStr | Human GV oocytes generated by mitotically active germ cells obtained from follicular aspirates |
title_full_unstemmed | Human GV oocytes generated by mitotically active germ cells obtained from follicular aspirates |
title_short | Human GV oocytes generated by mitotically active germ cells obtained from follicular aspirates |
title_sort | human gv oocytes generated by mitotically active germ cells obtained from follicular aspirates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4928061/ https://www.ncbi.nlm.nih.gov/pubmed/27357640 http://dx.doi.org/10.1038/srep28218 |
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