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组蛋白去乙酰化酶7调节肿瘤坏死因子-α介导的对睾丸间质细胞类固醇生成的抑制作用。

HDAC7 modulates TNF-α-mediated suppression of Leydig cell steroidogenesis.

作者信息

Sadasivam Mohanraj, Ramatchandirin Balamurugan, Balakrishnan Sivasangari, Prahalathan Chidambaram

机构信息

Department of Biochemistry, Bharathidasan University, Tiruchirappalli, 620 024, India.

出版信息

Mol Cell Biochem. 2015 Aug;406(1-2):83-90. doi: 10.1007/s11010-015-2426-y. Epub 2015 Apr 28.

Abstract

The pro-inflammatory cytokine tumor necrosis factor-alpha (TNF-α) has an inhibitory role in gonadal functions particularly in the steroidogenesis of Leydig cells. In the present study, we demonstrate that TNF-α activates histone deacetylases 7 (HDAC7), which regulates the expression of steroidogenic enzyme genes in Leydig cells. LC-540 Leydig cells were treated with TNF-α (10 ng/ml) for different time intervals. TNF-α treatment significantly suppressed histone H3 acetylation and methylation and, concomitantly, increased the total histone deacetylases activity in LC-540 Leydig cells. RT-PCR and western blot analysis revealed that HDAC7 was up-regulated in TNF-α-treated cells. Our results also demonstrated that an siRNA-mediated knockdown of HDAC7 restores the expression of steroidogenic proteins in TNF-α-treated Leydig cells. These findings provide valuable information that TNF-α-mediated suppression of steroidogenesis involves HDAC7 in Leydig cells.

摘要

促炎细胞因子肿瘤坏死因子-α(TNF-α)对性腺功能具有抑制作用,尤其是对睾丸间质细胞的类固醇生成。在本研究中,我们证明TNF-α可激活组蛋白去乙酰化酶7(HDAC7),该酶可调节睾丸间质细胞中类固醇生成酶基因的表达。用TNF-α(10 ng/ml)处理LC-540睾丸间质细胞不同时间间隔。TNF-α处理显著抑制了组蛋白H3的乙酰化和甲基化,并同时增加了LC-540睾丸间质细胞中总的组蛋白去乙酰化酶活性。逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹分析显示,在TNF-α处理的细胞中HDAC7上调。我们的结果还表明,小干扰RNA(siRNA)介导的HDAC7敲低可恢复TNF-α处理的睾丸间质细胞中类固醇生成蛋白的表达。这些发现提供了有价值的信息,即TNF-α介导的类固醇生成抑制涉及睾丸间质细胞中的HDAC7。

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