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The role of pituitary gonadotropins and intraovarian regulators in follicle development: A mini‐review

BACKGROUND: The process of follicle development is tightly regulated by pituitary gonadotropins (follicle‐stimulating hormone [FSH] and luteinizing hormone [LH]) and intraovarian regulators (eg, steroids, growth factors, and cytokines). METHODS: This review outlines recent findings on the mechanisms...

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Autores principales: Orisaka, Makoto, Miyazaki, Yumiko, Shirafuji, Aya, Tamamura, Chiyo, Tsuyoshi, Hideaki, Tsang, Benjamin K., Yoshida, Yoshio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022101/
https://www.ncbi.nlm.nih.gov/pubmed/33850449
http://dx.doi.org/10.1002/rmb2.12371
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author Orisaka, Makoto
Miyazaki, Yumiko
Shirafuji, Aya
Tamamura, Chiyo
Tsuyoshi, Hideaki
Tsang, Benjamin K.
Yoshida, Yoshio
author_facet Orisaka, Makoto
Miyazaki, Yumiko
Shirafuji, Aya
Tamamura, Chiyo
Tsuyoshi, Hideaki
Tsang, Benjamin K.
Yoshida, Yoshio
author_sort Orisaka, Makoto
collection PubMed
description BACKGROUND: The process of follicle development is tightly regulated by pituitary gonadotropins (follicle‐stimulating hormone [FSH] and luteinizing hormone [LH]) and intraovarian regulators (eg, steroids, growth factors, and cytokines). METHODS: This review outlines recent findings on the mechanisms of human follicle development, based on the research on animal models such as mice, rats, cows, and sheep. MAIN FINDINGS: Phosphatidylinositol 3‐kinase/protein kinase B signaling pathway and anti‐Müllerian hormone are involved in primordial follicle activation during the gonadotropin‐independent phase. The intraovarian regulators, such as androgen, insulin‐like growth factor system, activin, oocyte‐derived factors (growth differentiation factor‐9 and bone morphogenetic protein 15), and gap junction membrane channel protein (connexin), play a central role in the acquisition of FSH dependence in preantral follicles during the gonadotropin‐responsive phase. Antral follicle development can be divided into FSH‐dependent growth and LH‐dependent maturation. The indispensable tetralogy for follicle selection and final maturation of antral follicles involves (a) acquisition of LH dependence, (b) greater capacity for E2 production, (c) activation of the IGF system, and (d) an antiapoptotic follicular microenvironment. CONCLUSION: We reproductive endocrinologists should accumulate further knowledge from animal model studies to develop methods that promote early folliculogenesis and connect to subsequent gonadotropin therapy in infertile women.
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spelling pubmed-80221012021-04-12 The role of pituitary gonadotropins and intraovarian regulators in follicle development: A mini‐review Orisaka, Makoto Miyazaki, Yumiko Shirafuji, Aya Tamamura, Chiyo Tsuyoshi, Hideaki Tsang, Benjamin K. Yoshida, Yoshio Reprod Med Biol Mini Reviews BACKGROUND: The process of follicle development is tightly regulated by pituitary gonadotropins (follicle‐stimulating hormone [FSH] and luteinizing hormone [LH]) and intraovarian regulators (eg, steroids, growth factors, and cytokines). METHODS: This review outlines recent findings on the mechanisms of human follicle development, based on the research on animal models such as mice, rats, cows, and sheep. MAIN FINDINGS: Phosphatidylinositol 3‐kinase/protein kinase B signaling pathway and anti‐Müllerian hormone are involved in primordial follicle activation during the gonadotropin‐independent phase. The intraovarian regulators, such as androgen, insulin‐like growth factor system, activin, oocyte‐derived factors (growth differentiation factor‐9 and bone morphogenetic protein 15), and gap junction membrane channel protein (connexin), play a central role in the acquisition of FSH dependence in preantral follicles during the gonadotropin‐responsive phase. Antral follicle development can be divided into FSH‐dependent growth and LH‐dependent maturation. The indispensable tetralogy for follicle selection and final maturation of antral follicles involves (a) acquisition of LH dependence, (b) greater capacity for E2 production, (c) activation of the IGF system, and (d) an antiapoptotic follicular microenvironment. CONCLUSION: We reproductive endocrinologists should accumulate further knowledge from animal model studies to develop methods that promote early folliculogenesis and connect to subsequent gonadotropin therapy in infertile women. John Wiley and Sons Inc. 2021-02-13 /pmc/articles/PMC8022101/ /pubmed/33850449 http://dx.doi.org/10.1002/rmb2.12371 Text en © 2021 The Authors. Reproductive Medicine and Biology published by John Wiley & Sons Australia, Ltd on behalf of Japan Society for Reproductive Medicine. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Mini Reviews
Orisaka, Makoto
Miyazaki, Yumiko
Shirafuji, Aya
Tamamura, Chiyo
Tsuyoshi, Hideaki
Tsang, Benjamin K.
Yoshida, Yoshio
The role of pituitary gonadotropins and intraovarian regulators in follicle development: A mini‐review
title The role of pituitary gonadotropins and intraovarian regulators in follicle development: A mini‐review
title_full The role of pituitary gonadotropins and intraovarian regulators in follicle development: A mini‐review
title_fullStr The role of pituitary gonadotropins and intraovarian regulators in follicle development: A mini‐review
title_full_unstemmed The role of pituitary gonadotropins and intraovarian regulators in follicle development: A mini‐review
title_short The role of pituitary gonadotropins and intraovarian regulators in follicle development: A mini‐review
title_sort role of pituitary gonadotropins and intraovarian regulators in follicle development: a mini‐review
topic Mini Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8022101/
https://www.ncbi.nlm.nih.gov/pubmed/33850449
http://dx.doi.org/10.1002/rmb2.12371
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