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Role of transcription factors Ad4bp/SF-1 and DAX-1 in steroidogenesis and spermatogenesis in human testicular development and idiopathic azoospermia

Background:  Ad4bp/SF‐1 and DAX‐1 are orphan members of the nuclear hormone receptor superfamily of transcription factors. In order to obtain better understandings of human testicular steroidogenesis and spermatogenesis, we examined the expression levels of both factors in human normal and idiopathi...

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Published in:International journal of urology 2006-06, Vol.13 (6), p.785-793
Main Authors: KOJIMA, YOSHIYUKI, SASAKI, SHOICHI, HAYASHI, YUTARO, UMEMOTO, YUKIHIRO, MOROHASHI, KEN-ICHIRO, KOHRI, KENJIRO
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Language:English
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Summary:Background:  Ad4bp/SF‐1 and DAX‐1 are orphan members of the nuclear hormone receptor superfamily of transcription factors. In order to obtain better understandings of human testicular steroidogenesis and spermatogenesis, we examined the expression levels of both factors in human normal and idiopathic azoospermic testes and investigated their physical meaning. Methods:  First, we examined the expression level of Ad4bp/SF‐1 and DAX‐1 by quantitative reverse transcription–polymerase chain reaction (RT–PCR), immunohistochemistry and western blotting analysis using eight normal human testicular tissues from infants to adults. Second, we performed quantitative RT–PCR using testicular biopsy samples obtained from 22 idiopathic azoospermic patients to examine the expression of Ad4bp/SF‐1 and DAX‐1, and analysed the correlation between the expression levels of both factors and the serum hormone levels or histological evaluation to study their potential correlation with steroidogenesis and spermatogenesis on idiopathic azoospermia. Results:  The expression levels of both factors in the normal testes increased with testicular development. Ad4bp/SF‐1 was abundantly expressed in Leydig cell, whereas DAX‐1 was expressed in Sertoli cells. The expression level of Ad4bp/SF‐1 in idiopathic azoospermic patients testes positively correlated with serum testosterone (P 
ISSN:0919-8172
1442-2042
DOI:10.1111/j.1442-2042.2006.01403.x