Hydrogen peroxide enhances TRAIL-induced cell death through up-regulation of DR5 in human astrocytic cells

被引:29
作者
Kwon, Daeho [1 ]
Choi, Kyungsun [2 ]
Choi, Chulhee [2 ]
Benveniste, Etty N. [3 ]
机构
[1] Korea Univ, Med Res Ctr Environm Toxicogenom & Proteom, Coll Med, Seoul 136705, South Korea
[2] Korea Adv Inst Sci & Technol, Dept Bio & Brain Engn, Taejon 305701, South Korea
[3] Univ Alabama Birmingham, Dept Cell Biol, Birmingham, AL 35294 USA
基金
美国国家卫生研究院;
关键词
TRAIL; ROS; DR5; cell death; neuroimmunology; astrocytes;
D O I
10.1016/j.bbrc.2008.05.148
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The central nervous system (CNS) is particularly vulnerable to reactive oxygen species (ROS), which have been implicated in the pathogenesis of various neurological disorders. The TNF superfamily of cytokines, especially tumor necrosis factor-related apoptosis-inducing ligand (TRAIL), induces caspase-dependent cell death and is also implicated in various neurodegenerative diseases. In this study, we investigated the relationship between ROS and TRAIL-induced cell death. Exposure to hydrogen peroxide (H2O2) (100 mu M) sensitized human astrocytic cells to TRAIL-induced cell death (up to 7-fold induction). To delineate the molecular mechanisms responsible for H2O2-induced sensitization, we examined expression of various genes (Caspase-8, Fas, FasL, DR4, DR5, DcR1, DcR2, TRAIL, TNFRp55) related to TRAIL-induced cell death. Treatment with H2O2 significantly increased DR5 mRNA and protein expression in a time- and dose-dependent manner. H2O2-mediated cell death was blocked upon treatment with DR5:Fc protein, a TRAIL-specific antagonistic protein. These findings collectively suggest that oxidative stress sensitizes human astroglial cells to TRAIL-induced cell death through up-regulation of DR5 expression, (c) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:870 / 874
页数:5
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