Triphlorethol-A induces heme oxygenase-1 via activation of ERK and NF-E2 related factor 2 transcription factor

被引:65
作者
Kang, Kyoung Ah
Lee, Kyoung Hwa
Park, Jae Woo
Lee, Nam Ho
Na, Hye Kyung
Surh, Young Joon
You, Ho Jin
Chung, Myung Hee
Hyun, Jin Won [1 ]
机构
[1] Jeju Natl Univ, Dept Biochem, Coll Med, Cheju 690756, South Korea
[2] Jeju Natl Univ, Appl Radiol Sci Res Inst, Cheju 690756, South Korea
[3] Jeju Natl Univ, Dept Nucl & Energy Engn, Cheju 690756, South Korea
[4] Jeju Natl Univ, Dept Chem, Coll Nat Sci, Cheju 690756, South Korea
[5] Seoul Natl Univ, Coll Pharm, Lab Biochem & Mol Toxicol, Seoul 151742, South Korea
[6] Chosun Univ, Coll Med, Dept Pharmacol, Kwangju 501759, South Korea
[7] Seoul Natl Univ, Coll Med, Dept Pharmacol, Seoul 110799, South Korea
关键词
triphlorethol-A; heme oxygenase-1; NF-E2 related factor 2; antioxidant response element;
D O I
10.1016/j.febslet.2007.04.022
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
Triphlorethol-A, phlorotannin found in Ecklonia cava, induced heine oxygenase-1 (HO-1) expression at mRNA and protein levels, leading to increased HO-I activity. Transcription factor NF-E2 related factor 2 (Nrf2) regulates antioxidant response element (ARE) of phase 2 detoxifying and antioxidant enzymes. Triphlorethol-A increased nuclear translocation, ARE binding, and transcriptional activity of Nrf2. Triphlorethol-A exhibited activation of ERK and U0126, inhibitor of ERK kinase, suppressed triphlorethol-A induced activation of Nrf2, finally decreased HO-1 protein level. Taken together, these data suggest that triphlorethol-A augments cellular antioxidant defense capacity through induction of HO-I via ERK-Nrf2-ARE signaling pathway, thereby protecting cells from oxidative stress. (C) 2007 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:2000 / 2008
页数:9
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