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A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty

In cyclic females, FSH stimulates ovarian estradiol (E2) production and follicular growth up to the terminal stage. A transient elevation in circulating FSH and E2 levels occurs shortly after birth. But what could be the action of FSH on the ovary during this period, and in particular how it stimula...

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Autores principales: François, Charlotte M., Petit, Florence, Giton, Frank, Gougeon, Alain, Ravel, Célia, Magre, Solange, Cohen-Tannoudji, Joëlle, Guigon, Céline J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387682/
https://www.ncbi.nlm.nih.gov/pubmed/28397811
http://dx.doi.org/10.1038/srep46222
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author François, Charlotte M.
Petit, Florence
Giton, Frank
Gougeon, Alain
Ravel, Célia
Magre, Solange
Cohen-Tannoudji, Joëlle
Guigon, Céline J.
author_facet François, Charlotte M.
Petit, Florence
Giton, Frank
Gougeon, Alain
Ravel, Célia
Magre, Solange
Cohen-Tannoudji, Joëlle
Guigon, Céline J.
author_sort François, Charlotte M.
collection PubMed
description In cyclic females, FSH stimulates ovarian estradiol (E2) production and follicular growth up to the terminal stage. A transient elevation in circulating FSH and E2 levels occurs shortly after birth. But what could be the action of FSH on the ovary during this period, and in particular how it stimulates ovarian steroidogenesis without supporting terminal follicular maturation is intriguing. By experimentally manipulating FSH levels, we demonstrate in mice that the mid-infantile elevation in FSH is mandatory for E2 production by the immature ovary, but that it does not stimulate follicle growth. Importantly, FSH increases aromatase expression to stimulate E2 synthesis, however it becomes unable to induce cyclin D2, a major driver of granulosa cell proliferation. Besides, although FSH prematurely induces luteinizing hormone (LH) receptor expression in granulosa cells, LH pathway is not functional in these cells to induce their terminal differentiation. In line with these results, supplying infantile mice with a superovulation regimen exacerbates E2 production, but it does not stimulate the growth of follicles and it does not induce ovulation. Overall, our findings unveil a regulation whereby high postnatal FSH concentrations ensure the supply of E2 required for programming adult reproductive function without inducing follicular maturation before puberty.
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spelling pubmed-53876822017-04-12 A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty François, Charlotte M. Petit, Florence Giton, Frank Gougeon, Alain Ravel, Célia Magre, Solange Cohen-Tannoudji, Joëlle Guigon, Céline J. Sci Rep Article In cyclic females, FSH stimulates ovarian estradiol (E2) production and follicular growth up to the terminal stage. A transient elevation in circulating FSH and E2 levels occurs shortly after birth. But what could be the action of FSH on the ovary during this period, and in particular how it stimulates ovarian steroidogenesis without supporting terminal follicular maturation is intriguing. By experimentally manipulating FSH levels, we demonstrate in mice that the mid-infantile elevation in FSH is mandatory for E2 production by the immature ovary, but that it does not stimulate follicle growth. Importantly, FSH increases aromatase expression to stimulate E2 synthesis, however it becomes unable to induce cyclin D2, a major driver of granulosa cell proliferation. Besides, although FSH prematurely induces luteinizing hormone (LH) receptor expression in granulosa cells, LH pathway is not functional in these cells to induce their terminal differentiation. In line with these results, supplying infantile mice with a superovulation regimen exacerbates E2 production, but it does not stimulate the growth of follicles and it does not induce ovulation. Overall, our findings unveil a regulation whereby high postnatal FSH concentrations ensure the supply of E2 required for programming adult reproductive function without inducing follicular maturation before puberty. Nature Publishing Group 2017-04-11 /pmc/articles/PMC5387682/ /pubmed/28397811 http://dx.doi.org/10.1038/srep46222 Text en Copyright © 2017, The Author(s) 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
François, Charlotte M.
Petit, Florence
Giton, Frank
Gougeon, Alain
Ravel, Célia
Magre, Solange
Cohen-Tannoudji, Joëlle
Guigon, Céline J.
A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty
title A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty
title_full A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty
title_fullStr A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty
title_full_unstemmed A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty
title_short A novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty
title_sort novel action of follicle-stimulating hormone in the ovary promotes estradiol production without inducing excessive follicular growth before puberty
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5387682/
https://www.ncbi.nlm.nih.gov/pubmed/28397811
http://dx.doi.org/10.1038/srep46222
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