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凋亡敏感基因蛋白对一氧化氮诱导的细胞凋亡的调控

Regulation of nitric oxide-induced apoptosis by sensitive to apoptosis gene protein.

作者信息

Yang Eun Sun, Park Jeen-Woo

机构信息

School of Life Sciences and Biotechnology, College of Natural Sciences, Kyungpook National University, Taegu 702701, Korea.

出版信息

Free Radic Res. 2006 Mar;40(3):279-84. doi: 10.1080/10715760500511500.

Abstract

Sensitive to apoptosis gene (SAG) protein, a novel zinc RING finger protein that protects mammalian cells from apoptosis by redox reagents, is a metal chelator and a potential reactive oxygen species (ROS) scavenger, but its antioxidant properties have not been completely defined. Nitric oxide (NO), a radical species produced by many types of cells, is known to play a critical role in many regulatory processes, yet it may also participate in collateral reactions at higher concentrations, leading to cellular oxidative stress. In this report, we demonstrate that modulation of SAG expression in U937 cells regulates NO-induced apoptosis. When we examined the protective role of SAG against NO-induced apoptosis with U937 cells transfected with the cDNA for SAG, a clear inverse relationship was observed between the amount of SAG expressed in target cells and their susceptibility to apoptosis. We also observed the significant decrease in the endogenous production of ROS and oxidative DNA damage in SAG-overexpressed cells compared to control cells upon exposure to NO. These results suggest that SAG plays an important protective role in NO-induced apoptosis, presumably, through regulating the cellular redox status.

摘要

对凋亡敏感基因(SAG)蛋白是一种新型锌指环蛋白,可通过氧化还原试剂保护哺乳动物细胞免于凋亡,它是一种金属螯合剂和潜在的活性氧(ROS)清除剂,但其抗氧化特性尚未完全明确。一氧化氮(NO)是多种细胞产生的自由基,已知在许多调节过程中起关键作用,但在较高浓度下它也可能参与附带反应,导致细胞氧化应激。在本报告中,我们证明U937细胞中SAG表达的调节可调控NO诱导的凋亡。当我们用SAG的cDNA转染U937细胞来检测SAG对NO诱导凋亡的保护作用时,在靶细胞中表达的SAG量与其对凋亡的敏感性之间观察到明显的负相关关系。与对照细胞相比,我们还观察到在暴露于NO时,SAG过表达细胞中ROS的内源性产生和氧化性DNA损伤显著降低。这些结果表明,SAG在NO诱导的凋亡中起重要的保护作用,大概是通过调节细胞氧化还原状态来实现的。

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