Calcium-Dependent NOX5 Nicotinamide Adenine Dinucleotide Phosphate Oxidase Contributes to Vascular Oxidative Stress in Human Coronary Artery Disease

被引:248
作者
Guzik, Tomasz J. [1 ,2 ]
Chen, Wei [1 ]
Gongora, Maria C. [1 ]
Guzik, Bartlomiej [2 ]
Lob, Heinrich E. [1 ]
Mangalat, Deepa [1 ]
Hoch, Nyssa [1 ]
Dikalov, Sergey [1 ]
Rudzinski, Pawel [2 ]
Kapelak, Boguslaw [2 ]
Sadowski, Jerzy [3 ]
Harrison, David G. [1 ]
机构
[1] Emory Univ, Div Cardiol, Dept Med, Sch Med, Atlanta, GA 30322 USA
[2] Jagiellonian Univ, Sch Med, Dept Pharmacol & Internal Med, Krakow, Poland
[3] Jagiellonian Univ, Sch Med, Dept Cardiovasc Surg & Transplantat, Krakow, Poland
关键词
reactive oxygen species; NOX5; NADPH oxidase; atherosclerosis; coronary artery disease;
D O I
10.1016/j.jacc.2008.07.063
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Objectives This study sought to examine the expression and activity of the calcium-dependent nicotinamide adenine dinucleotide phosphate ( NADPH) oxidase ( NOX) in human atherosclerotic coronary arteries. Background The NOX-based NADPH oxidases are major sources of reactive oxygen species (ROS) in human vessels. Several NOX homologues have been identified, but their relative contribution to vascular ROS production in coronary artery disease (CAD) is unclear; NOX5 is a unique homolog in that it is calcium dependent and thus could be activated by vasoconstrictor hormones. Its presence has not yet been studied in human vessels. Methods Coronary arteries from patients undergoing cardiac transplantation with CAD or without CAD were studied; NOX5 was quantified and visualized using Western blotting, immunofluorescence, and quantitative real-time polymerase chain reaction. Calcium-dependent NADPH oxidase activity, corresponding greatly to NOX5 activity, was measured by electron paramagnetic resonance. Results Both Western blotting and quantitative real-time polymerase chain reaction indicated a marked increase in NOX5 protein and messenger ribonucleic acid ( mRNA) in CAD versus non-CAD vessels. Calcium-dependent NADPH-driven production of ROS in vascular membranes, reflecting NOX5 activity, was increased 7-fold in CAD and correlated significantly with NOX5 mRNA levels among subjects. Immunofluorescence showed that NOX5 was expressed in the endothelium in the early lesions and in vascular smooth muscle cells in the advanced coronary lesions. Conclusions These studies identify NOX5 as a novel, calcium-dependent source of ROS in atherosclerosis. (J Am Coll Cardiol 2008; 52: 1803-9) (c) 2008 by the American College of Cardiology Foundation.
引用
收藏
页码:1803 / 1809
页数:7
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