Expression of NADH/NADPH oxidase p22phox in human coronary arteries

被引:238
作者
Azumi, H
Inoue, N
Takeshita, S
Rikitake, Y
Kawashima, S
Hayashi, Y
Itoh, H
Yokoyama, M
机构
[1] Kobe Univ, Sch Med, Dept Internal Med 1, Kobe, Hyogo 650, Japan
[2] Kobe Univ, Sch Med, Dept Pathol 1, Kobe, Hyogo 650, Japan
关键词
atherosclerosis; free radicals; coronary disease;
D O I
10.1161/01.CIR.100.14.1494
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 ana 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.
引用
收藏
页码:1494 / 1498
页数:5
相关论文
共 9 条
  • [1] HUMAN SMOOTH-MUSCLE MYOSIN HEAVY-CHAIN ISOFORMS AS MOLECULAR MARKERS FOR VASCULAR DEVELOPMENT AND ATHEROSCLEROSIS
    AIKAWA, M
    SIVAM, PN
    KUROO, M
    KIMURA, K
    NAKAHARA, K
    TAKEWAKI, S
    UEDA, M
    YAMAGUCHI, H
    YAZAKI, Y
    PERIASAMY, M
    NAGAI, R
    [J]. CIRCULATION RESEARCH, 1993, 73 (06) : 1000 - 1012
  • [2] Expression of a functional neutrophil-type NADPH oxidase in cultured rat coronary microvascular endothelial cells
    Bayraktutan, U
    Draper, N
    Lang, D
    Shah, AM
    [J]. CARDIOVASCULAR RESEARCH, 1998, 38 (01) : 256 - 262
  • [3] CYTOCHROME B-558 ALPHA-SUBUNIT CLONING AND EXPRESSION IN RAT AORTIC SMOOTH-MUSCLE CELLS
    FUKUI, T
    LASSEGUE, B
    KAI, H
    ALEXANDER, RW
    GRIENDLING, KK
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1995, 1231 (03): : 215 - 219
  • [4] Redox control of vascular smooth muscle proliferation
    Griendling, KK
    Ushio-Fukai, M
    [J]. JOURNAL OF LABORATORY AND CLINICAL MEDICINE, 1998, 132 (01): : 9 - 15
  • [5] IMAJOHOHMI S, 1992, J BIOL CHEM, V267, P180
  • [6] Polymorphism of the NADH/NADPH oxidase p22 phox gene in patients with coronary artery disease
    Inoue, N
    Kawashima, S
    Kanazawa, K
    Yamada, S
    Akita, H
    Yokoyama, M
    [J]. CIRCULATION, 1998, 97 (02) : 135 - 137
  • [7] Kanazawa K, 1996, AM J PATHOL, V148, P1949
  • [8] Circumferential stress and matrix metalloproteinase 1 in human coronary atherosclerosis - Implications for plaque rupture
    Lee, RT
    Schoen, FJ
    Loree, HM
    Lark, MW
    Libby, P
    [J]. ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1996, 16 (08) : 1070 - 1073
  • [9] p22(phox) is a critical component of the superoxide-generating NADH/NADPH oxidase system and regulates angiotensin II-induced hypertrophy in vascular smooth muscle cells
    UshioFukai, M
    Zafari, AM
    Fukui, T
    Ishizaka, N
    Griendling, KK
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (38) : 23317 - 23321