Of marsupials and men: "Backdoor" dihydrotestosterone synthesis in male sexual differentiation
Publisher DOI
PubMed ID
23376007
Abstract
Following development of the fetal bipotential gonad into a testis, male genital differentiation requires testicular androgens. Fetal Leydig cells produce testosterone that is converted to dihydrotestosterone in genital skin, resulting in labio-scrotal fusion. An alternative 'backdoor' pathway of dihydrotestosterone synthesis that bypasses testosterone has been described in marsupials, but its relevance to human biology has been uncertain. The classic and backdoor pathways share many enzymes, but a 3α-reductase, AKR1C2, is unique to the backdoor pathway. Human AKR1C2 mutations cause disordered sexual differentiation, lending weight to the idea that both pathways are required for normal human male genital development. These observations indicate that fetal dihydrotestosterone acts both as a hormone and as a paracrine factor, substantially revising the classic paradigm for fetal male sexual development.
Date Issued
2013
Publication Type
Article
Language(s)
en
Author(s)
Biason-Lauber, Anna | |
Miller, Walter L | |
Pandey, Amit V |
Additional Credits
Journal
Molecular and cellular endocrinology
Publisher
Elsevier Ireland
ISSN
0303-7207
Access(Rights)
metadata.only