G蛋白偶联胆汁酸受体
生物
法尼甾体X受体
胆汁酸
胆酸
肝受体同系物-1
核受体
脱氧胆酸
受体
内分泌学
内科学
小异二聚体伴侣
信号转导
骨化三醇受体
细胞生物学
转录因子
生物化学
维生素D与神经学
基因
医学
作者
Marine Baptissart,Aurélie Vega,Emmanuelle Martinot,Aurélien Pommier,Sander M. Houten,Geoffroy Marceau,Angélique De Haze,Silvère Baron,Kristina Schoonjans,Jean‐Marc A. Lobaccaro,David H. Volle
出处
期刊:Hepatology
[Lippincott Williams & Wilkins]
日期:2014-05-03
卷期号:60 (3): 1054-1065
被引量:51
摘要
Bile acids (BAs) are signaling molecules that are involved in many physiological functions, such as glucose and energy metabolism. These effects are mediated through activation of the nuclear and membrane receptors, farnesoid X receptor (FXR-α) and TGR5 (G-protein-coupled bile acid receptor 1; GPBAR1). Although both receptors are expressed within the testes, the potential effect of BAs on testis physiology and male fertility has not been explored thus far. Here, we demonstrate that mice fed a diet supplemented with cholic acid have reduced fertility subsequent to testicular defects. Initially, germ cell sloughing and rupture of the blood-testis barrier occur and are correlated with decreased protein accumulation of connexin-43 (Cx43) and N-cadherin, whereas at later stages, apoptosis of spermatids is observed. These abnormalities are associated with increased intratesticular BA levels in general and deoxycholic acid, a TGR5 agonist, in particular. We demonstrate here that Tgr5 is expressed within the germ cell lineage, where it represses Cx43 expression through regulation of the transcriptional repressor, T-box transcription factor 2 gene. Consistent with this finding, mice deficient for Tgr5 are protected against the deleterious testicular effects of BA exposure. Conclusions : These data identify the testis as a new target of BAs and emphasize TGR5 as a critical element in testicular pathophysiology. This work may open new perspectives on the potential effect of BAs on testis physiology during liver dysfunction. (Hepatology 2014;60:1054-1065)
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