TY - JOUR
T1 - Nrf2-Keap1 defines a physiologically important stress response mechanism
AU - Motohashi, Hozumi
AU - Yamamoto, Masayuki
N1 - Funding Information:
We thank Paul Talalay, Tom Kensler, John Hayes, Doug Engel and our laboratory members for generous advice. We also thank Ken Itoh and Akira Kobayashi for discussion and advice, and Kit I. Tong for help. We apologize for not citing many important publications in this emerging field owing to the space limitation. This work has been supported in part by grants from ERATO-JST, MEXT, MHLW and JSPS.
PY - 2004/11
Y1 - 2004/11
N2 - 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.
AB - 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.
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U2 - 10.1016/j.molmed.2004.09.003
DO - 10.1016/j.molmed.2004.09.003
M3 - Review article
C2 - 15519281
AN - SCOPUS:7244253081
SN - 1471-4914
VL - 10
SP - 549
EP - 557
JO - Trends in Molecular Medicine
JF - Trends in Molecular Medicine
IS - 11
ER -