Aging decreases expression and activity of glutathione peroxidase-1 in human endothelial progenitor cells

被引:56
作者
He, Tongrong [1 ]
Joyner, Michael J. [1 ]
Katusic, Zvonimir S. [1 ]
机构
[1] Mayo Clin, Coll Med, Dept Anesthesiol & Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
基金
美国国家卫生研究院;
关键词
Aging; Endothelial progenitor cells; GPX1; Oxidative stress; Human subjects; AGE-RELATED-CHANGES; SUPEROXIDE-DISMUTASE; OXIDATIVE STRESS; LIFE-SPAN; CATALASE; MICE; TRANSPLANTATION; OVEREXPRESSION; OUTGROWTH; GPX1;
D O I
10.1016/j.mvr.2009.08.009
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The mechanisms underlying effects of aging on functions of pro-angiogenic endothelial progenitor cells (EPCs) are poorly understood. Previous studies demonstrated that human EPCs express high levels of antioxidant enzymes as compared to mature endothelial cells. Here, we hypothesized that aging impairs antioxidant capacity of EPCs. So called "early EPCs" derived from cultured blood mononuclear cells were obtained from healthy young (average = 24 years old) and old (average = 72 years old) subjects. In EPCs of old subjects, the levels of glutathione peroxidase-1 (GPX1) protein and enzymatic activity were significantly reduced. The serum selenium levels in young and old subjects were not significantly different. Increasing selenium concentration in the cell culture also did not affect the protein levels of GPX1, suggesting the reduced GPX1 in old subject's EPCs is selenium independent. Expressions of catalase, Mn-superoxide dismutase (MnSOD). and CuZnSOD were not affected by aging. EPCs of old subjects were more sensitive to oxidative stress induced by H2O2 as compared with EPCs of young subjects, suggesting that impairment of GPX1 during aging may contribute to low survival ability of EPCs in response to oxidative stress. The results indicate that GPX1 may represent a potential therapeutic target for enhancement of regenerative capacity of EPCs in old subjects. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:447 / 452
页数:6
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