ROS generation by nonphagocytic NADPH oxidase: Potential relevance in diabetic nephropathy

被引:244
作者
Li, JM [1 ]
Shah, AM [1 ]
机构
[1] Kings Coll London, GKT Sch Med, Dept Cardiol, London SE5 9PJ, England
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2003年 / 14卷
关键词
D O I
10.1097/01.ASN.0000077406.67663.E7
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Oxidative stress has emerged as an important pathogenic factor in the development of long-term complications, such as atherosclerosis and nephropathy, in patients with diabetes. Whereas multiple enzymes and processes can contribute to oxidative stress, recent studies indicate that a multicomponent phagocyte-type NADPH oxidase is a major source of reactive oxygen species (ROS) production in many nonphagocytic cells, including fibroblasts, vascular smooth muscle cells, endothelial cells, renal mesangial cells, and tubular cells. Under physiologic conditions, nonphagocytic NADPH oxidases have very low-level constitutive activity. However, enzyme activity can be upregulated both acutely and chronically in response to stimuli such as growth factors, cytokines, high glucose, and hyperlipidemia. ROS production by the oxidase may serve a signaling role or may lead to oxidative damage. This article reviews current knowledge of the nonphagocyte-NADPH oxidases at both structural and biochemical levels and discusses the possible role of these enzymes in the pathophysiology of diabetic nephropathy.
引用
收藏
页码:S221 / S226
页数:6
相关论文
共 58 条
[1]   Vascular endothelial growth factor induces manganese-superoxide dismutase expression in endothelial cells by a Rac1-regulated NADPH oxidase-dependent mechanism [J].
Abid, MR ;
Tsai, JC ;
Spokes, KC ;
Deshpande, SS ;
Irani, K ;
Aird, WC .
FASEB JOURNAL, 2001, 15 (11) :2548-+
[2]   Free radicals mediate endothelial dysfunction of coronary arterioles in diabetes [J].
Ammar, RF ;
Gutterman, DD ;
Brooks, LA ;
Dellsperger, KC .
CARDIOVASCULAR RESEARCH, 2000, 47 (03) :595-601
[3]   NADPH oxidase: An update [J].
Babior, BM .
BLOOD, 1999, 93 (05) :1464-1476
[4]   The neutrophil NADPH oxidase [J].
Babior, BM ;
Lambeth, JD ;
Nauseef, W .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2002, 397 (02) :342-344
[5]   p47phox is required for atherosclerotic lesion progression in ApoE-/- mice [J].
Barry-Lane, PA ;
Patterson, C ;
van der Merwe, M ;
Hu, ZY ;
Holland, SM ;
Yeh, ETH ;
Runge, MS .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (10) :1513-1522
[6]   Molecular characterization and localization of the NAD(P)H oxidase components gp91-phox and p22-phox in endothelial cells [J].
Bayraktutan, U ;
Blayney, L ;
Shah, AM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (08) :1903-1911
[7]   Pivotal role of a gp91phox-containing NADPH oxidase in angiotensin II-induced cardiac hypertrophy in mice [J].
Bendall, JK ;
Cave, AC ;
Heymes, C ;
Gall, N ;
Shah, AM .
CIRCULATION, 2002, 105 (03) :293-296
[8]   Investigation into the sources of superoxide in human blood vessels - Angiotensin II increases superoxide production in human internal mammary arteries [J].
Berry, C ;
Hamilton, CA ;
Brosnan, J ;
Magill, FG ;
Berg, GA ;
McMurray, JJV ;
Dominiczak, AF .
CIRCULATION, 2000, 101 (18) :2206-2212
[9]   The vascular NADPH oxidase subunit p47phox is involved in redox-mediated gene expression [J].
Brandes, RP ;
Miller, FJ ;
Beer, S ;
Haendeler, J ;
Hoffmann, J ;
Ha, T ;
Holland, SM ;
Görlach, A ;
Busse, R .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (11) :1116-1122
[10]   Expression and cellular localization of classic NADPH oxidase subunits in the spontaneously hypertensive rat kidney [J].
Chabrashvili, T ;
Tojo, A ;
Onozato, ML ;
Kitiyakara, C ;
Quinn, MT ;
Fujita, T ;
Welch, WJ ;
Wilcox, CS .
HYPERTENSION, 2002, 39 (02) :269-274