Nrf2-Keap1 defines a physiologically important stress response mechanism

被引:1458
作者
Motohashi, H
Yamamoto, M [1 ]
机构
[1] Univ Tsukuba, Japan Sci & Technol Corp, Ctr Tsukuba Adv Res Alliance Exploratory Res Adv, Tsukuba, Ibaraki 3058577, Japan
[2] Univ Tsukuba, Japan Sci & Technol Corp, Environm Response Project, Tsukuba, Ibaraki 3058577, Japan
基金
日本学术振兴会;
关键词
D O I
10.1016/j.molmed.2004.09.003
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 transcription factor Nrf2 regulates the basal and inducible expression of numerous detoxifying and antioxidant genes. The cytoplasmic protein Keap1 interacts with Nrf2 and represses its function. Analysis of keap1-knockout mice provides solid evidence that Keap1 acts as a negative regulator of Nrf2 and as a sensor of xenobiotic and oxidative stresses. The simultaneous ablation of the keap1 and nrf2 genes reversed all apparent phenotypes of the Keap1-deficient mice, suggesting that NrF2 is a primary target of Keap1. The Nrf2-Keap1 system is now recognized as one of the major cellular defence mechanisms against oxidative and xenobiotic stresses. Furthermore, extensive studies have suggested that the Nrf2-Keap1 system contributes to protection against various pathologies, including carcinogenesis, liver toxicity, respiratory distress and inflammation.
引用
收藏
页码:549 / 557
页数:9
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