Effect of peroxisome proliferators on Leydig cell peripheral-type benzodiazepine receptor gene expression, hormone-stimulated cholesterol transport, and steroidogenesis: Role of the peroxisome proliferator-activator receptor alpha

Gazouli, M; Yao, ZX; Boujrad, N; Corton, JC; Culty, M; Papadopoulos, V

HERO ID

674161

Reference Type

Journal Article

Year

2002

Language

English

PMID

12072389

HERO ID 674161
In Press No
Year 2002
Title Effect of peroxisome proliferators on Leydig cell peripheral-type benzodiazepine receptor gene expression, hormone-stimulated cholesterol transport, and steroidogenesis: Role of the peroxisome proliferator-activator receptor alpha
Authors Gazouli, M; Yao, ZX; Boujrad, N; Corton, JC; Culty, M; Papadopoulos, V
Journal Endocrinology
Volume 143
Issue 7
Page Numbers 2571-2583
Abstract In this study, we hypothesized that many of the reported effects of phthalate esters and other peroxisome proliferators (PPs) in the testis are mediated by members of the PP- activated receptor (PPAR) family of transcription factors through alterations in proteins involved in steroidogenesis. Exposure of Leydig cells to PPs prevented cholesterol transport into the mitochondria after hormonal stimulation and inhibited steroid synthesis, without altering total cell protein synthesis or mitochondrial and DNA integrity. PPs also reduced the levels of the cholesterol-binding protein peripheral-type benzodiazepine receptor (PBR) because of a direct transcriptional inhibition of PBR gene expression in MA-10 Leydig cells. MA-10 cells contain mRNAs for PPARalpha and PPARbeta/delta, but not for PPARgamma. In vivo treatment of mice with PPs resulted in the reduction of both testis PBR mRNA and circulating testosterone levels, in agreement with the proposed role of PBR in steroidogenesis. By contrast, liver PBR mRNA levels were increased, in agreement with the proposed role of PBR in cell growth/tumor formation in nonsteroidogenic tissues. However, PPs did not inhibit testosterone production and testis PBR expression in PPARalpha-null mice. These results suggest that the antiandrogenic effect of PPs is mediated by a PPARalpha-dependent inhibition of Leydig cell PBR gene expression.
Doi 10.1210/endo.143.7.8895
Pmid 12072389
Wosid WOS:000176550400016
Is Certified Translation No
Dupe Override No
Comments Source: Web of Science WOS:000176550400016
Is Public Yes
Language Text English
Keyword *Androgen Antagonists; Animals; Biological Transport, Active/drug effects; Blotting, Northern; Carrier Proteins/biosynthesis/genetics; Catalase/metabolism; Cell Survival/drug effects; Cells, Cultured; Cholesterol/*metabolism; Chorionic Gonadotropin/antagonists & inhibitors; DNA Damage/drug effects; Electrophoresis, Polyacrylamide Gel; Gene Expression Regulation/drug effects; Humans; Leydig Cells/drug effects/*metabolism; Male; Mice; Mitochondria/drug effects/metabolism; Peroxisome Proliferators/*pharmacology; RNA, Messenger/biosynthesis; Radioimmunoassay; Radioligand Assay; Rats; Receptors, Cytoplasmic and Nuclear/drug effects/*metabolism; Receptors, GABA-A/*biosynthesis/drug effects/genetics; Reverse Transcriptase Polymerase Chain Reaction; Steroids/*biosynthesis; Transcription Factors/drug effects/*metabolism; Transfection; 0 (Androgen Antagonists); 0 (Carrier Proteins); 0 (Chorionic Gonadotropin); 0 (Peroxisome Proliferators); 0 (RNA, Messenger); 0 (Receptors, Cytoplasmic and Nuclear); 0 (Receptors, GABA-A); 0 (Steroids); 0 (Transcription Factors); 0 (cholesterol-binding protein); 57-88-5 (Cholesterol); EC 1.11.1.6 (Catalase)
Is Qa No