Affiliation:
1. From the First Department of Internal Medicine (N.I., S.T., Y.R., S.K., M.Y.) and the First Department of Pathology (H.A., Y.H., H.I.), Kobe University School of Medicine, Kobe, Japan.
Abstract
Background
—NADH/NADPH oxidase is an important source of superoxide in the vasculature. Recently, we found that polymorphism of the gene p22
phox
, a critical component of this oxidase, is associated with a risk of coronary artery disease. The aim of this study was to investigate the localization of p22
phox
in human coronary arteries and to examine its difference in expression between nonatherosclerotic and atherosclerotic coronary arteries.
Methods and Results
—Using coronary artery sections from autopsied cases (n=11), the expression of p22
phox
was examined by immunohistochemistry and Western blotting. In nonatherosclerotic coronary arteries, p22
phox
was weakly expressed, mainly in the adventitia. In atherosclerotic coronary arteries, intensive immunoreactivity was detected in neointimal and medial smooth muscle cells and infiltrating macrophages in hypercellular regions and at the shoulder region. Semiquantitative analysis and Western blotting showed that the expression of p22
phox
in atherosclerotic coronary arteries was more pronounced than that in nonatherosclerotic arteries. Double staining revealed p22
phox
expression in adventitial fibroblasts, smooth muscle cells, macrophages in the neointima and media, and endothelial cells.
Conclusions
—As atherosclerosis progressed, the expression of p22
phox
increased through the vessel wall. p22
phox
might participate in the pathogenesis and pathophysiology of atherosclerotic coronary disease.
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Cited by
240 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献