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Bile acids alter male fertility through G-protein-coupled bile acid receptor 1 signaling pathways in mice

机译:胆汁酸通过G蛋白偶联的胆汁酸受体1信号通路改变小鼠的生育能力

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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. 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
机译:胆汁酸(BAs)是涉及许多生理功能(例如葡萄糖和能量代谢)的信号分子。这些作用通过核和膜受体,法呢类X受体(FXR-α)和TGR5(G蛋白偶联胆汁酸受体1; GPBAR1)的激活来介导。尽管两种受体均在睾丸内表达,但迄今为止,BAs对睾丸生理和男性生育力的潜在影响尚未得到探讨。在这里,我们证明了饲喂添加了胆酸的饮食的小鼠睾丸缺损后的生育力降低。最初,生殖细胞脱落和血液-睾丸屏障破裂发生,并与连接蛋白43(Cx43)和N-钙黏着蛋白的蛋白质积累减少有关,而在后期,观察到精子细胞的凋亡。这些异常通常与睾丸内BA水平升高有关,尤其与TGR5激动剂脱氧胆酸有关。我们在这里证明,Tgr5在生殖细胞谱系中表达,在那里它通过调节转录抑制因子T-box转录因子2基因来抑制Cx43表达。与此发现一致的是,Tgr5缺陷型小鼠受到BA暴露的有害睾丸保护。这些数据将睾丸确定为BA的新靶标,并强调TGR5是睾丸病理生理学中的关键要素。这项工作可能会为BAs在肝功能异常期间对睾丸生理的潜在影响开辟新的观点。

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