1,2,3,4,6-penta-O-galloyl-β-D-glucose up-regulates heme oxygenase-1 expression by stimulating Nrf2 nuclear translocation in an extracellular signal-regulated kinase-dependent manner in HepG2 cells

被引:34
作者
Pae, Hyun-Ock [1 ]
Oh, Gi-Su [1 ]
Leong, Sun-Oh [1 ]
Jeong, Gil-Saeng [1 ]
Lee, Bok-Soo [1 ]
Choi, Byung-Min [1 ]
Lee, Ho-Sub [1 ]
Chung, Hun-Taeg [1 ]
机构
[1] Wonkwang Univ, Sch Med, Med Resources Res Inst, Dept Microbiol & Immunol, Iksan 570749, Chonbug, South Korea
关键词
1,2,3,4,6-penta-O-galloyl-beta-D-glucose; heme oxygenase-1; oxidative stress; hepatoprotection;
D O I
10.3748/wjg.v12.i2.214
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
AIM: To examine the potency of 1,2,3,4,6-penta-O-galloyl-beta-D-glucose (PGG) as a hepatic heme oxygenase-1 (HO-1) inducer and its regulation in HepG2 cells. METHODS: Expression of HO-1 and NF-E2-related factor 2 (Nrf2) and activation of mitogen-activated protein (MAP) kinases were analyzed by Western blot, immunofluorescence assay, and flow cytometry. Transfections of HO-1 gene, small interfering RNAs for HO-1 and Nrf2, and dominant-negative gene for MAP/extracellular signal-regulated kinase (ERK) were carried out to dissect the signaling pathways leading to HO-1 expression in HepG 2 cells. RESULTS: PGG up-regulated HO-1 expression and this expression conferred cytoprotection against oxidative injury induced by t-butyl hydroperoxide. Moreover, PGG induced Nrf2 nuclear translocation, which was found to be an upstream step of PGG-induced HO-1 expression, and ERK activation, of which pathway was involved in PGG-induced Nrf2 nuclear translocation, HO-1 expression and cytoprotection. CONCLUSION: PGG up-regulates HO-1 expression by stimulating Nrf2 nuclear translocation in an ERK-dependent manner, and HO-1 expression by PGG may serve as one of the important mechanisms for its hepatoprotective effects. (c) 2006 The WJG Press. All rights reserved.
引用
收藏
页码:214 / 221
页数:8
相关论文
共 33 条
[1]
Alam J, 2000, J BIOL CHEM, V275, P27694
[2]
Nrf2, a Cap'n'Collar transcription factor, regulates induction of the heme oxygenase-1 gene [J].
Alam, J ;
Stewart, D ;
Touchard, C ;
Boinapally, S ;
Choi, AMK ;
Cook, JL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (37) :26071-26078
[3]
Transcriptional regulation of the heme oxygenase-1 gene via the stress response element pathway [J].
Alam, J ;
Cook, JL .
CURRENT PHARMACEUTICAL DESIGN, 2003, 9 (30) :2499-2511
[4]
Curcurnin activates the haem oxygenase-1 gene via regulation of Nrf2 and the antioxidant-responsive element [J].
Balogun, E ;
Hoque, M ;
Gong, PF ;
Killeen, E ;
Green, CJ ;
Foresti, R ;
Alam, J ;
Motterlini, R .
BIOCHEMICAL JOURNAL, 2003, 371 :887-895
[5]
Nitric oxide stimulates Nrf2 nuclear translocation in vascular endothelium [J].
Buckley, BJ ;
Marshall, ZM ;
Whorton, AR .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 307 (04) :973-979
[6]
Induction of detoxifying enzymes by garlic organosulfur compounds through transcription factor Nrf2: Effect of chemical structure and stress signals [J].
Chen, C ;
Pung, D ;
Leong, V ;
Hebbar, V ;
Shen, GX ;
Nair, S ;
Li, W ;
Kong, ANT .
FREE RADICAL BIOLOGY AND MEDICINE, 2004, 37 (10) :1578-1590
[7]
Induction of G1 arrest and apoptosis in human Jurkat T cells by pentagalloylglucose through inhibiting proteasome activity and elevating p27Kip1, p21Cip1/WAF1, and Bax proteins [J].
Chen, WJ ;
Lin, JK .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (14) :13496-13505
[8]
Induction of cytoprotective genes through Nrf2/antioxidant response element pathway: A new therapeutic approach for the treatment of inflammatory diseases [J].
Chen, XL ;
Kunsch, C .
CURRENT PHARMACEUTICAL DESIGN, 2004, 10 (08) :879-891
[9]
Nitric oxide-mediated cytoprotection of hepatocytes from glucose deprivation-induced cytotoxicity: Involvement of heme oxygenase-1 [J].
Choi, BM ;
Pae, HO ;
Kim, YM ;
Chung, HT .
HEPATOLOGY, 2003, 37 (04) :810-823
[10]
1,2,3,4,6-Penta-O-galloyl-beta-D-glucose protects rat neuronal cells (Neuro 2A) from hydrogen peroxide-mediated cell death via the induction of heme oxygenase-1 [J].
Choi, BM ;
Kim, HJ ;
Oh, GS ;
Pae, HO ;
Oh, H ;
Jeong, S ;
Kwon, TO ;
Kim, YM ;
Chung, HT .
NEUROSCIENCE LETTERS, 2002, 328 (02) :185-189