Cell survival responses to environmental stresses via the Keap1-Nrf2-ARE pathway

被引：2957

作者：

Kensler, Thomas W. ^{[1
]}

Wakabayash, Nobunao ^{[1
]}

Biswal, Shyam ^{[1
]}

机构：

[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Environm Hlth Sci, Baltimore, MD 21205 USA

来源：

ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY | 2007年 / 47卷

关键词：

antioxidant response element; oxidative stress; cytoprotection; gene expression; knockout mice;

D O I：

10.1146/annurev.pharmtox.46.120604.141046

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

Keap1-Nrf2-ARE signaling plays a significant role in protecting cells 1 from endogenous and exogenous stresses. The development of Nrf2 knockout mice has provided key insights into the toxicological importance of this pathway. These mice are more sensitive to the hepatic, pulmonary, ovarian, and neurotoxic consequences of acute exposures to environmental agents and drugs, inflammatory stresses, as well as chronic exposures to cigarette smoke and other carcinogens. Under quiescent conditions, the transcription factor Nrf2 interacts with the actin-anchored protein Keap1, largely localized in the cytoplasm. This quenching interaction maintains low basal expression of Nrf2-regulated genes. However, upon recognition of chemical signals imparted by oxidative and electrophilic molecules, Nrf2 is released from Keap1, escapes proteasomal degradation, translocates to the nucleus, and transactivates the expression of several dozen cytoprotective genes that enhance cell survival. This review highlights the key elements in this adaptive response to protection against acute and chronic cell injury provoked by environmental stresses.

引用

页码：89 / 116

页数：28

共 110 条

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