Carbon monoxide mediates heme oxygenase 1 induction via Nrf2 activation in hepatoma cells

被引:85
作者
Lee, BS
Heo, J
Kim, YM
Shim, SM
Pae, HO
Kim, YM
Chung, HT [1 ]
机构
[1] Wonkwang Univ, Sch Med, Dept Microbiol & Immunol, Med Resources Res Inst, Chonbuk 570749, South Korea
[2] FCB Pharmicell Co Ltd, Stem Cell Therapy Inst, Sungnam 462120, Kyungki Do, South Korea
[3] Kangwon Natl Univ, Coll Med, Dept Mol & Cellular Biochem, Chunchon, Kangwon Do, South Korea
[4] Kangwon Natl Univ, Vasc Syst Res Ctr, Chunchon, Kangwon Do, South Korea
关键词
carbon monoxide; tricarbonyl dichlororuthenium (II) dimmer (RuCO); heme oxygenase 1; nitric oxide/inducible NO synthase; mitogenactivated protein kinases; NF-E2-related factor; anti-oxidant response element;
D O I
10.1016/j.bbrc.2006.03.058
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
Carbon monoxide (CO) and nitric oxide (NO) are two gas molecules which have cytoprotective functions against oxidative stress and inflammatory responses in many cell types. Currently, it is known that NO produced by nitric oxide synthase (NOS) induces heme oxygenase 1 (HO1) expression and CO produced by the HO1 inhibits inducible NOS expression. Here.. we first show CO-mediated HO1 induction and its possible mechanism in human hepatocytes. Exposure of HepG2 cells or primary hepatocytes to CO resulted in dramatic induction of HO1 in dose- and time-dependent manner. The CO-mediated HO1 induction was abolished by MAP kinase inhibitors (MAPKs) but not affected by inhibitors of PI3 kinase or NF-kappa B. In addition, CO induced the nuclear translocation and accumulation of Nrf2, which suppressed by MAPKs inhibitors. Taken together, we suggest that CO induces Nrf2 activation via MAPKs signaling pathways, thereby resulting in HO1 expression in HepG2 cells. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:965 / 972
页数:8
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