Hypoxia-inducible factor-1 (HIF-1) pathway activation by quercetin in human lens epithelial cells

被引:18
作者
Radreau, Pauline [1 ]
Rhodes, Jeremy D. [2 ]
Mithen, Richard F. [3 ]
Kroon, Paul A. [3 ]
Sanderson, Julie [1 ]
机构
[1] Univ E Anglia, Sch Pharm, Norwich NR4 7TJ, Norfolk, England
[2] Univ E Anglia, Sch Biol Sci, Norwich NR4 7TJ, Norfolk, England
[3] Inst Food Res, Norwich NR4 7UA, Norfolk, England
基金
英国生物技术与生命科学研究理事会;
关键词
quercetin; flavonoid; antioxidant; diet; lens; HIF-1; alpha; hypoxia; VEGF; ENDOTHELIAL GROWTH-FACTOR; NUCLEAR CATARACT; FLAVONOID INTAKE; HIF-1-ALPHA; EXPRESSION; OXIDATION; RISK; REGULATOR; PROTECT;
D O I
10.1016/j.exer.2009.08.011
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Quercetin is a dietary bioflavonoid which has been shown to inhibit lens opacification in a number of models of cataract. The objectives of this study were to determine gene expression changes in human lens epithelial cells in response to quercetin and to investigate in detail the mechanisms underlying the responses. FHL-124 cells were treated with quercetin (10 mu M) and changes in gene expression were measured by microarray. It was found that 65% of the genes with increased expression were regulated by the hypoxia-inducible factor-1 (HIF-1) pathway. Quercetin (10 and 30 mu M) induced a time-dependent increase in HIF-1 alpha protein levels. Quercetin (30 mu M) was also responsible for a rapid and long-lasting translocation of HIF-1 alpha from the cytoplasm to the nucleus. Activation of HIF-1 signaling by quercetin was confirmed by qRT-PCR which showed upregulation of the HIF-1 regulated genes EPO, VEGF, PGK1 and BNIP3. Analysis of medium taken from FHL-124 cells showed a sustained dose-dependent increase in VEGF secretion following quercetin treatment. The quercetin-induced increase and nuclear translocation of HIF-1 alpha was reversed by addition of excess iron (100 mu M). These results demonstrate that quercetin activates the HIF-1 signaling pathway in human lens epithelial cells. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:995 / 1002
页数:8
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