Anti-Müllerian Hormone Signal Transduction involved in Müllerian Duct Regression

Over seventy years ago it was proposed that the fetal testis produces a hormone distinct from testosterone that is required for complete male sexual development. At the time the hormone had not yet been identified but was invoked by Alfred Jost to explain why the Müllerian duct, which develops into...

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Published in:Frontiers in endocrinology (Lausanne) Vol. 13; p. 905324
Main Author: Cate, Richard L.
Format: Journal Article
Language:English
Published: Frontiers Media S.A 02-06-2022
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Summary:Over seventy years ago it was proposed that the fetal testis produces a hormone distinct from testosterone that is required for complete male sexual development. At the time the hormone had not yet been identified but was invoked by Alfred Jost to explain why the Müllerian duct, which develops into the female reproductive tract, regresses in the male fetus. That hormone, anti-Müllerian hormone (AMH), and its specific receptor, AMHR2, have now been extensively characterized and belong to the transforming growth factor-β families of protein ligands and receptors involved in growth and differentiation. Much is now known about the downstream events set in motion after AMH engages AMHR2 at the surface of specific Müllerian duct cells and initiates a cascade of molecular interactions that ultimately terminate in the nucleus as activated transcription factors. The signals generated by the AMH signaling pathway are then integrated with signals coming from other pathways and culminate in a complex gene regulatory program that redirects cellular functions and fates and leads to Müllerian duct regression.
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Edited by: Nathalie Josso, Institut National de la Santé et de la Recherche Médicale (INSERM), France
This article was submitted to Reproduction, a section of the journal Frontiers in Endocrinology
Reviewed by: Rachel Mullen, University of Texas MD Anderson Cancer Center, United States; Tom Thompson, University of Cincinnati, United States
ISSN:1664-2392
1664-2392
DOI:10.3389/fendo.2022.905324