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Tamoxifen Activates Dormant Primordial Follicles in Mouse Ovaries

Our previous study found that 17β-estradiol (E(2)) suppresses primordial follicle activation and growth in cultured mouse ovaries. In this study, we administered tamoxifen, an estrogen receptor antagonist, into the abdominal cavity of mice to clarify the relationship between primordial follicle acti...

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Autores principales: Wei, Wei, Komatsu, Kouji, Osuka, Satoko, Murase, Tomohiko, Bayasula, Bayasula, Nakanishi, Natsuki, Nakamura, Tomoko, Goto, Maki, Iwase, Akira, Masubuchi, Satoru, Kajiyama, Hiroaki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734234/
https://www.ncbi.nlm.nih.gov/pubmed/35212933
http://dx.doi.org/10.1007/s43032-022-00896-0
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author Wei, Wei
Komatsu, Kouji
Osuka, Satoko
Murase, Tomohiko
Bayasula, Bayasula
Nakanishi, Natsuki
Nakamura, Tomoko
Goto, Maki
Iwase, Akira
Masubuchi, Satoru
Kajiyama, Hiroaki
author_facet Wei, Wei
Komatsu, Kouji
Osuka, Satoko
Murase, Tomohiko
Bayasula, Bayasula
Nakanishi, Natsuki
Nakamura, Tomoko
Goto, Maki
Iwase, Akira
Masubuchi, Satoru
Kajiyama, Hiroaki
author_sort Wei, Wei
collection PubMed
description Our previous study found that 17β-estradiol (E(2)) suppresses primordial follicle activation and growth in cultured mouse ovaries. In this study, we administered tamoxifen, an estrogen receptor antagonist, into the abdominal cavity of mice to clarify the relationship between primordial follicle activation and the physiological concentration of E(2) in mouse ovaries. The results showed that tamoxifen promoted primordial follicle activation. Administration of tamoxifen promoted degradation of the extracellular matrix surrounding primordial follicles in the ovaries. Furthermore, tamoxifen decreased the expression of stefin A, an inhibitor of cathepsins that digest some proteins and extracellular matrix, in the ovaries. Mechanical stress produced by the extracellular matrix reportedly suppresses the activation of primordial follicles. The collective results show that tamoxifen can promote primordial follicle activation through the degradation of the extracellular matrix surrounding primordial follicles. Our results indicate that E(2) suppresses primordial follicle activation in vivo and that tamoxifen may be useful as a therapeutic agent against infertility. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43032-022-00896-0.
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spelling pubmed-97342342022-12-11 Tamoxifen Activates Dormant Primordial Follicles in Mouse Ovaries Wei, Wei Komatsu, Kouji Osuka, Satoko Murase, Tomohiko Bayasula, Bayasula Nakanishi, Natsuki Nakamura, Tomoko Goto, Maki Iwase, Akira Masubuchi, Satoru Kajiyama, Hiroaki Reprod Sci Reproductive Biology: Original Article Our previous study found that 17β-estradiol (E(2)) suppresses primordial follicle activation and growth in cultured mouse ovaries. In this study, we administered tamoxifen, an estrogen receptor antagonist, into the abdominal cavity of mice to clarify the relationship between primordial follicle activation and the physiological concentration of E(2) in mouse ovaries. The results showed that tamoxifen promoted primordial follicle activation. Administration of tamoxifen promoted degradation of the extracellular matrix surrounding primordial follicles in the ovaries. Furthermore, tamoxifen decreased the expression of stefin A, an inhibitor of cathepsins that digest some proteins and extracellular matrix, in the ovaries. Mechanical stress produced by the extracellular matrix reportedly suppresses the activation of primordial follicles. The collective results show that tamoxifen can promote primordial follicle activation through the degradation of the extracellular matrix surrounding primordial follicles. Our results indicate that E(2) suppresses primordial follicle activation in vivo and that tamoxifen may be useful as a therapeutic agent against infertility. GRAPHICAL ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43032-022-00896-0. Springer International Publishing 2022-02-25 /pmc/articles/PMC9734234/ /pubmed/35212933 http://dx.doi.org/10.1007/s43032-022-00896-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Reproductive Biology: Original Article
Wei, Wei
Komatsu, Kouji
Osuka, Satoko
Murase, Tomohiko
Bayasula, Bayasula
Nakanishi, Natsuki
Nakamura, Tomoko
Goto, Maki
Iwase, Akira
Masubuchi, Satoru
Kajiyama, Hiroaki
Tamoxifen Activates Dormant Primordial Follicles in Mouse Ovaries
title Tamoxifen Activates Dormant Primordial Follicles in Mouse Ovaries
title_full Tamoxifen Activates Dormant Primordial Follicles in Mouse Ovaries
title_fullStr Tamoxifen Activates Dormant Primordial Follicles in Mouse Ovaries
title_full_unstemmed Tamoxifen Activates Dormant Primordial Follicles in Mouse Ovaries
title_short Tamoxifen Activates Dormant Primordial Follicles in Mouse Ovaries
title_sort tamoxifen activates dormant primordial follicles in mouse ovaries
topic Reproductive Biology: Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734234/
https://www.ncbi.nlm.nih.gov/pubmed/35212933
http://dx.doi.org/10.1007/s43032-022-00896-0
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