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阳精胶囊通过促进类固醇生成急性调节蛋白(StAR)表达抑制睾丸间质细胞凋亡及促进睾酮合成的机制

Mechanisms of Yangjing Capsule in Leydig Cell Apoptosis and Testosterone Synthesis via Promoting StAR Expression.

作者信息

Sun Dalin, Dong Weihang, Jin Baofang, Chen Guanghui, Cai Bin, Deng Weimin, Cui Yugui, Jin Yihan

机构信息

Andrology Department of Integrative Medicine, Zhongda Hospital, School of Medicine, Southeast University.

Medical College of Qinghai University.

出版信息

Biol Pharm Bull. 2018 Sep 1;41(9):1401-1405. doi: 10.1248/bpb.b18-00205. Epub 2018 Jul 6.

DOI:10.1248/bpb.b18-00205
PMID:29984732
Abstract

The present study aims to investigate the roles of steroidogenic acute regulatory protein (StAR) in Yangjing Capsule (YC) induced anti-apoptotic effects on Leydig cells and the related mechanism. Leydig tumor cells (MLTC-1) were cultured and treated with YC, and immunofluorescence assay was performed to examine the expression of StAR; furthermore, luciferase reporter assay was conducted to evaluate the impact of YC on StAR promoter; next, MLTC-1 cells were treated with StAR small interfering RNA (siRNA), and flow cytometry was carried out to examine the effect of StAR siRNA on the apoptosis of the cells; furthermore, quantitative (q)RT-PCR and Western blot methods was used to determine the expression of StAR and apoptosis related molecules Bcl-2, Bax and Caspase-3 on both mRNA and protein levels in different groups; finally the secretion of testosterone in different groups was examined by radioimmunoassay. We observed that the YC can increase the expression of StAR in a dose-dependent manner, and YC can activate the promoter of StAR; moreover, transfection of StAR siRNA can block YC induced anti-apoptotic effects and increased production of testosterone. In conclusion, our results suggested that YC might suppress the apoptosis of MLTC-1 cells and enhance the production of testosterone through regulating the expression of StAR.

摘要

本研究旨在探讨类固醇生成急性调节蛋白(StAR)在阳精胶囊(YC)诱导的对睾丸间质细胞抗凋亡作用中的作用及相关机制。培养睾丸间质瘤细胞(MLTC-1)并用YC处理,进行免疫荧光分析以检测StAR的表达;此外,进行荧光素酶报告基因分析以评估YC对StAR启动子的影响;接下来,用StAR小干扰RNA(siRNA)处理MLTC-1细胞,进行流式细胞术检测StAR siRNA对细胞凋亡的影响;此外,采用定量(q)RT-PCR和蛋白质印迹法在mRNA和蛋白质水平上测定不同组中StAR以及凋亡相关分子Bcl-2、Bax和Caspase-3的表达;最后通过放射免疫分析法检测不同组中睾酮的分泌。我们观察到YC能以剂量依赖的方式增加StAR的表达,且YC能激活StAR的启动子;此外,转染StAR siRNA可阻断YC诱导的抗凋亡作用并增加睾酮的产生。总之,我们的结果表明YC可能通过调节StAR的表达来抑制MLTC-1细胞的凋亡并增强睾酮的产生。

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