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In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human

In the mammalian ovaries, dormant primordial follicles represent the reproductive reserve of individual females. Recently, stimulating the activation of primordial follicles in vitro has been practiced, making the utilization of those dormant follicles to treat female infertility possible. However,...

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Autores principales: Zhang, Jiawei, Yan, Lei, Wang, Yibo, Zhang, Shuo, Xu, Xueqiang, Dai, Yanli, Zhao, Shidou, Li, Zhen, Zhang, Yan, Xia, Guoliang, Qin, Yingying, Zhang, Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520080/
https://www.ncbi.nlm.nih.gov/pubmed/32997412
http://dx.doi.org/10.1002/ctm2.182
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author Zhang, Jiawei
Yan, Lei
Wang, Yibo
Zhang, Shuo
Xu, Xueqiang
Dai, Yanli
Zhao, Shidou
Li, Zhen
Zhang, Yan
Xia, Guoliang
Qin, Yingying
Zhang, Hua
author_facet Zhang, Jiawei
Yan, Lei
Wang, Yibo
Zhang, Shuo
Xu, Xueqiang
Dai, Yanli
Zhao, Shidou
Li, Zhen
Zhang, Yan
Xia, Guoliang
Qin, Yingying
Zhang, Hua
author_sort Zhang, Jiawei
collection PubMed
description In the mammalian ovaries, dormant primordial follicles represent the reproductive reserve of individual females. Recently, stimulating the activation of primordial follicles in vitro has been practiced, making the utilization of those dormant follicles to treat female infertility possible. However, there are still lacks of effective upstream molecule and strategy to elevate follicle activation in vivo. In the current study, we revealed that growth factor EGF improved a transiently primordial follicle activation in mice by elevating the CDC42‐PI3K signaling activity, and EGF treatment also improved the activation and development of human follicles in ovarian cortical pieces. Using a liquid‐solid phase transition bio‐gel as a carrier, an efficient in vivo activation system was established by ovarian topical EGF administration to living mice. We found that EGF treatment led to an increase of primordial follicle activation in short time but had no effect on long‐term fertility in females. By establishing an inducible premature ovarian insufficiency (POI) mouse model through selectively ablating growing follicles in Zp3‐Cre;iDTR mice, we further revealed that our in vivo EGF treatment system improved primordial follicle activation and ovulation of POI ovaries significantly. Taken together, our results revealed that in situ ovarian EGF administration could improve the activation of primordial follicles in living animals, and manipulating activation and development of primordial follicles in vivo might be an efficient approach to improve reproductive health in women.
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spelling pubmed-75200802020-09-30 In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human Zhang, Jiawei Yan, Lei Wang, Yibo Zhang, Shuo Xu, Xueqiang Dai, Yanli Zhao, Shidou Li, Zhen Zhang, Yan Xia, Guoliang Qin, Yingying Zhang, Hua Clin Transl Med Research Articles In the mammalian ovaries, dormant primordial follicles represent the reproductive reserve of individual females. Recently, stimulating the activation of primordial follicles in vitro has been practiced, making the utilization of those dormant follicles to treat female infertility possible. However, there are still lacks of effective upstream molecule and strategy to elevate follicle activation in vivo. In the current study, we revealed that growth factor EGF improved a transiently primordial follicle activation in mice by elevating the CDC42‐PI3K signaling activity, and EGF treatment also improved the activation and development of human follicles in ovarian cortical pieces. Using a liquid‐solid phase transition bio‐gel as a carrier, an efficient in vivo activation system was established by ovarian topical EGF administration to living mice. We found that EGF treatment led to an increase of primordial follicle activation in short time but had no effect on long‐term fertility in females. By establishing an inducible premature ovarian insufficiency (POI) mouse model through selectively ablating growing follicles in Zp3‐Cre;iDTR mice, we further revealed that our in vivo EGF treatment system improved primordial follicle activation and ovulation of POI ovaries significantly. Taken together, our results revealed that in situ ovarian EGF administration could improve the activation of primordial follicles in living animals, and manipulating activation and development of primordial follicles in vivo might be an efficient approach to improve reproductive health in women. John Wiley and Sons Inc. 2020-09-27 /pmc/articles/PMC7520080/ /pubmed/32997412 http://dx.doi.org/10.1002/ctm2.182 Text en © 2020 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhang, Jiawei
Yan, Lei
Wang, Yibo
Zhang, Shuo
Xu, Xueqiang
Dai, Yanli
Zhao, Shidou
Li, Zhen
Zhang, Yan
Xia, Guoliang
Qin, Yingying
Zhang, Hua
In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human
title In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human
title_full In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human
title_fullStr In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human
title_full_unstemmed In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human
title_short In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human
title_sort in vivo and in vitro activation of dormant primordial follicles by egf treatment in mouse and human
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7520080/
https://www.ncbi.nlm.nih.gov/pubmed/32997412
http://dx.doi.org/10.1002/ctm2.182
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