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.
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Univ Mississippi, Dept Pharmacognosy, University, MS 38677 USAUniv Mississippi, Dept Pharmacognosy, University, MS 38677 USA
Liu, Yang
Veena, Coothan K.
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Univ Mississippi, Dept Pharmacognosy, University, MS 38677 USAUniv Mississippi, Dept Pharmacognosy, University, MS 38677 USA
Veena, Coothan K.
Morgan, J. Brian
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Univ Mississippi, Dept Pharmacognosy, University, MS 38677 USAUniv Mississippi, Dept Pharmacognosy, University, MS 38677 USA
Morgan, J. Brian
Mohammed, Kaleem A.
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Univ Mississippi, Dept Pharmacognosy, University, MS 38677 USAUniv Mississippi, Dept Pharmacognosy, University, MS 38677 USA
Mohammed, Kaleem A.
Jekabsons, Mika B.
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Univ Mississippi, Dept Biol, University, MS 38677 USAUniv Mississippi, Dept Pharmacognosy, University, MS 38677 USA
Jekabsons, Mika B.
Nagle, Dale G.
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Univ Mississippi, Dept Pharmacognosy, University, MS 38677 USA
Univ Mississippi, Res Inst Pharmaceut Sci, Sch Pharm, University, MS 38677 USAUniv Mississippi, Dept Pharmacognosy, University, MS 38677 USA
Nagle, Dale G.
Zhou, Yu-Dong
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Univ Mississippi, Dept Pharmacognosy, University, MS 38677 USAUniv Mississippi, Dept Pharmacognosy, University, MS 38677 USA
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Univ Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Hlth Sci Ctr, Aurora, CO USAUniv Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Belibi, Franck
Zafar, Iram
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Univ Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Hlth Sci Ctr, Aurora, CO USAUniv Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Zafar, Iram
Ravichandran, Kameswaran
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Univ Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Hlth Sci Ctr, Aurora, CO USAUniv Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Ravichandran, Kameswaran
Segvic, Anamarija Bauer
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Zagreb Dubrava Univ Hosp, Sch Med, Zagreb, CroatiaUniv Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Segvic, Anamarija Bauer
Jani, Alkesh
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Univ Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Hlth Sci Ctr, Aurora, CO USAUniv Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Jani, Alkesh
Ljubanovic, Danica Galesic
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Zagreb Dubrava Univ Hosp, Sch Med, Zagreb, CroatiaUniv Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Ljubanovic, Danica Galesic
Edelstein, Charles L.
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Univ Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA
Hlth Sci Ctr, Aurora, CO USAUniv Colorado Denver, Div Renal Dis & Hypertens, Aurora, CO 80262 USA