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Up-regulation of Nrf2-mediated heme oxygenase-1 expression by eckol, a phlorotannin compound, through activation of Erk and PI3K/Akt

Cited 110 time in Web of Science Cited 116 time in Scopus
Authors
Kim, Ki Cheon; Kang, Kyoung Ah; Zhang, Rui; Piao, Mei Jing; Kim, Gi Young; Kang, Mi Young; Lee, Su Jae; Lee, Nam Ho; Surh, Young-Joon; Hyun, Jin Won
Issue Date
2010-02
Citation
International Journal of Biochemistry and Cell Biology, Vol.42 No.2, pp.297-305
Keywords
EckolHeme oxygenase-1NF-E2-related factor 2Oxidative stressCytoprotectionExtracellular regulated kinasePhosphatidylinositol 3-kinase
Abstract
The aim of the present study was to examine the cytoprotective effect of eckol, a phlorotannin found in Ecklonia cava and to elucidate underlying mechanisms. Heme oxygenase-1 (HO-1) is an important antioxidant enzyme that plays a role in cytoprotection against oxidative stress. Eckol-induced HO-1 expression both at the level of mRNA and protein in Chinese hamster lung fibroblast (V79-4) cells, resulting in increased HO-1 activity. The transcription factor NF-E2-related factor 2 (Nrf2) is a critical regulator of HO-1, achieved by binding to the antioxidant response element (ARE). Eckol treatment resulted in the enhanced level of phosphorylated form, nuclear translocation, ARE-binding, and transcriptional activity of Nrf2. Extracellular regulated kinase (Erk) and phosphaticylinositol 3-kinase (PI3K)/protein kinase B (PKB, Akt) contributed to ARE-driven HO-1 expression. Eckol activated both Erk and Akt, and treatments with U0126 (an Erk kinase inhibitor), LY294002 (a PI3K inhibitor), specific Erk1 siRNA, and Akt siRNA suppressed the eckol-induced activation of Nrf2, resulting in a decrease in HO-1 expression. ZnPP (a HO-1 inhibitor), HO-1 siRNA, and Nrf2 siRNA markedly abolished the cytoprotective effect of eckol against hydrogen peroxide-induced cell damage. Likewise, U0126 and LY294002 inhibited the eckol-induced cytoprotective effect against oxidative cell damage. These studies demonstrate that eckol attenuates oxidative stress by activating Nrf2-mediated HO-1 induction via Erk and PI3K/Akt signaling. (C) 2009 Elsevier Ltd. All rights reserved.
ISSN
1357-2725
URI
https://hdl.handle.net/10371/172647
DOI
https://doi.org/10.1016/j.biocel.2009.11.009
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Graduate School of Convergence Science and Technology (융합과학기술대학원)Dept. of Molecular and Biopharmaceutical Sciences (분자의학 및 바이오제약학과)Journal Papers (저널논문_분자의학 및 바이오제약학과)
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