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The Ras GTPase-activating-like Protein IQGAP1 Mediates Nrf2 Protein Activation via the Mitogen-activated Protein Kinase/Extracellular Signal-regulated Kinase (ERK) Kinase (MEK)-ERK Pathway
被引:46
|作者:
Cheung, Ka Lung
[1
,2
]
Lee, Jong Hun
[2
]
Shu, Limin
[2
]
Kim, Jung-Hwan
[2
]
Sacks, David B.
[3
]
Kong, Ah-Ng Tony
[2
]
机构:
[1] Rutgers State Univ, Ernest Mario Sch Pharm, Grad Program Pharmaceut Sci, Piscataway, NJ 08854 USA
[2] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Pharmaceut, Piscataway, NJ 08854 USA
[3] NIH, Dept Lab Med, Bethesda, MD 20892 USA
关键词:
ANTIOXIDANT RESPONSE ELEMENT;
BINDING PROTEIN;
NUCLEAR TRANSLOCATION;
OXIDATIVE STRESS;
HEME OXYGENASE-1;
GENE-EXPRESSION;
HEPG2;
CELLS;
CALMODULIN;
INDUCTION;
IDENTIFICATION;
D O I:
10.1074/jbc.M112.444182
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:
Nrf2 plays a critical role in the regulation of cellular oxidative stress. MEK-ERK activation has been shown to be one of the major pathways resulting in the activation of Nrf2 and induction of Nrf2 downstream targets, including phase II detoxifying/antioxidant genes in response to oxidative stress and xenobiotics. In this study, IQGAP1 (IQ motif-containing GTPase-activating protein 1), a new Nrf2 interaction partner that we have published previously, was found to modulate MEK-ERK-mediated Nrf2 activation and induction of phase II detoxifying/antioxidant genes. Nrf2 binds directly to the IQ domain (amino acids 699-905) of IQGAP1. Knockdown of IQGAP1 significantly attenuated phenethyl isothiocyanate-or MEK-mediated activation of the MEK-ERK-Nrf2 pathway. Knockdown of IQGAP1 also attenuated MEK-mediated increased stability of Nrf2, which in turn was associated with a decrease in the nuclear translocation of Nrf2 and a decrease in the expression of phase II detoxifying/antioxidant genes. In the aggregate, these results suggest that IQGAP1 may play an important role in the MEK-ERK-Nrf2 signaling pathway.
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页码:22378 / 22386
页数:9
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