Cited by 101Sexual Differentiation and DisordersSperm and Testicular FunctionHormonal and reproductive studies

Prostate formation in a marsupial is mediated by the testicular androgen 5α-androstane-3α,17β-diol

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Shaw, Geoffrey, Renfree, Marilyn B., Leihy, Michael W., Shackleton, Cedric H. L., Roitman, Esther, Wilson, Jean D.·2000·Proceedings of the National Academy of Sciences

Abstract

Development of the male urogenital tract in mammals is mediated by testicular androgens. It has been tacitly assumed that testosterone acts through its intracellular metabolite dihydrotestosterone (DHT) to mediate this process, but levels of these androgens are not sexually dimorphic in plasma at the time of prostate development. Here we show that the 3 alpha-reduced derivative of DHT, 5 alpha-androstane-3 alpha,17 beta-diol (5 alpha-adiol), is formed in testes of tammar wallaby pouch young and is higher in male than in female plasma in this species during early sexual differentiation. Administration of 5 alpha-adiol caused formation of prostatic buds in female wallaby pouch young, and in tissue minces of urogenital sinus and urogenital tubercle radioactive 5 alpha-adiol was converted to DHT, suggesting that circulating 5 alpha-adiol acts through DHT in target tissues. We conclude that circulating 5 alpha-adiol is a key hormone in male development.

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  • Normal masculinization of the fetus is dependent upon androgen secretion by the testis, and androgens act initially during a critical masculinization programming window.

    “Normal masculinization of the fetus is dependent upon androgen secretion by the testis, and androgens act initially during a critical masculinization programming window to ensure normal male reproductive development [3–5].”

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References 32 · Cited by 101

Research works printed but not linked: 1

  1. [8]Ryhorchuk A R, Shaw G, Butler C M, Renfree M B. J Androl. 1997;181:123–130. [PubMed] [Google Scholar]

Authors
Shaw, G., Renfree, M. B., Leihy, M. W., Shackleton, C. H. L., Roitman, E., & Wilson, J. D.
Affiliations
  • Department of Zoology, University of Melbourne, Victoria 3010, Australia; Children's Hospital Oakland Research Institute, 5700 Martin Luther King, Jr. Way, Oakland, CA 94609-1673; and Department of Internal Medicine, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390-8857
  • The University of Melbourne (AU)
Venue
Proceedings of the National Academy of Sciences
Published
2000-10-17
Volume
97
Issue
22
Pages
12256-12259
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2040536456
Cited by
101
References
32
Citations by year
2025: 1 · 2024: 1 · 2023: 3 · 2021: 2 · 2020: 2 · 2019: 6 · 2018: 3 · 2017: 1 · 2016: 4 · 2015: 3 · 2014: 6 · 2013: 3 · 2012: 3
FWCI
2.41
Type
journal article
Language
en
Open access
Locations
  • Proceedings of the National Academy of Sciences (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
  • Health Sciences › Medicine › Reproductive Medicine › Sperm and Testicular Function
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
Keywords
prostate development, 5α-androstane-3α,17β-diol, dihydrotestosterone, testicular androgens, marsupials, tammar wallaby, pouch young, urogenital development, sexual differentiation, urogenital sinus, androgen metabolism
MeSH terms
Animals, Female, Macropodidae, Male, Gas Chromatography-Mass Spectrometry, Pregnancy, Prostate, Testis, Androstane-3,17-diol

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