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Inhibition of EED activity enhances cell survival of female germline stem cell and improves the oocytes production during oogenesis in vitro
Ovarian organoids, based on female germline stem cells (FGSCs), are nowadays widely applied for reproductive medicine screening and exploring the potential mechanisms during mammalian oogenesis. However, there are still key issues that urgently need to be resolved in ovarian organoid technology, one...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874982/ https://www.ncbi.nlm.nih.gov/pubmed/36695089 http://dx.doi.org/10.1098/rsob.220211 |
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author | Wang, Jiapeng Fang, Junxian Feng, Mingqian Li, Liping Ma, Lixin Zhao, Xiaorong Dai, Yanfeng |
author_facet | Wang, Jiapeng Fang, Junxian Feng, Mingqian Li, Liping Ma, Lixin Zhao, Xiaorong Dai, Yanfeng |
author_sort | Wang, Jiapeng |
collection | PubMed |
description | Ovarian organoids, based on female germline stem cells (FGSCs), are nowadays widely applied for reproductive medicine screening and exploring the potential mechanisms during mammalian oogenesis. However, there are still key issues that urgently need to be resolved in ovarian organoid technology, one of which is to establish a culture system that effectively expands FGSCs in vitro, as well as maintaining the unipotentcy of FGSCs to differentiate into oocytes. Here, FGSCs were EED226 treated and processed for examination of proliferation and differentiation in vitro. According to the results, EED226 specifically increased FGSC survival by decreasing the enrichment of H3K27me3 on Oct4 promoter and exon, as well as enhancing OCT4 expression and inhibiting P53 and P63 expression. Notably, we also found that FGSCs with EED226 treatment differentiated into more oocytes during oogenesis in vitro, and the resultant oocytes maintained a low level of P63 versus control at early stage development. These results demonstrated that inhibition of EED activity appeared to promote the survival of FGSCs and markedly inhibited their apoptosis during in vitro differentiation. As a result of our study, we propose an effective culture strategy to culture FGSCs and obtain oocytes in vitro, which provides a new vision for oogenesis in vitro. |
format | Online Article Text |
id | pubmed-9874982 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-98749822023-01-25 Inhibition of EED activity enhances cell survival of female germline stem cell and improves the oocytes production during oogenesis in vitro Wang, Jiapeng Fang, Junxian Feng, Mingqian Li, Liping Ma, Lixin Zhao, Xiaorong Dai, Yanfeng Open Biol Research Ovarian organoids, based on female germline stem cells (FGSCs), are nowadays widely applied for reproductive medicine screening and exploring the potential mechanisms during mammalian oogenesis. However, there are still key issues that urgently need to be resolved in ovarian organoid technology, one of which is to establish a culture system that effectively expands FGSCs in vitro, as well as maintaining the unipotentcy of FGSCs to differentiate into oocytes. Here, FGSCs were EED226 treated and processed for examination of proliferation and differentiation in vitro. According to the results, EED226 specifically increased FGSC survival by decreasing the enrichment of H3K27me3 on Oct4 promoter and exon, as well as enhancing OCT4 expression and inhibiting P53 and P63 expression. Notably, we also found that FGSCs with EED226 treatment differentiated into more oocytes during oogenesis in vitro, and the resultant oocytes maintained a low level of P63 versus control at early stage development. These results demonstrated that inhibition of EED activity appeared to promote the survival of FGSCs and markedly inhibited their apoptosis during in vitro differentiation. As a result of our study, we propose an effective culture strategy to culture FGSCs and obtain oocytes in vitro, which provides a new vision for oogenesis in vitro. The Royal Society 2023-01-25 /pmc/articles/PMC9874982/ /pubmed/36695089 http://dx.doi.org/10.1098/rsob.220211 Text en © 2023 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Wang, Jiapeng Fang, Junxian Feng, Mingqian Li, Liping Ma, Lixin Zhao, Xiaorong Dai, Yanfeng Inhibition of EED activity enhances cell survival of female germline stem cell and improves the oocytes production during oogenesis in vitro |
title | Inhibition of EED activity enhances cell survival of female germline stem cell and improves the oocytes production during oogenesis in vitro |
title_full | Inhibition of EED activity enhances cell survival of female germline stem cell and improves the oocytes production during oogenesis in vitro |
title_fullStr | Inhibition of EED activity enhances cell survival of female germline stem cell and improves the oocytes production during oogenesis in vitro |
title_full_unstemmed | Inhibition of EED activity enhances cell survival of female germline stem cell and improves the oocytes production during oogenesis in vitro |
title_short | Inhibition of EED activity enhances cell survival of female germline stem cell and improves the oocytes production during oogenesis in vitro |
title_sort | inhibition of eed activity enhances cell survival of female germline stem cell and improves the oocytes production during oogenesis in vitro |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9874982/ https://www.ncbi.nlm.nih.gov/pubmed/36695089 http://dx.doi.org/10.1098/rsob.220211 |
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