Role of xanthine oxidoreductase and NAD(P)H oxidase in endothelial superoxide production in response to oscillatory shear stress

被引:373
作者
McNally, JS
Davis, ME
Giddens, DP
Saha, A
Hwang, JN
Dikalov, S
Jo, H
Harrison, DG
机构
[1] Emory Univ, Div Cardiol, Atlanta, GA 30322 USA
[2] Emory Univ, Mol & Syst Pharmacol Program, Atlanta, GA 30322 USA
[3] Georgia Tech, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30322 USA
[4] Atlanta Vet Hosp Med Ctr, Decatur, GA 30033 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2003年 / 285卷 / 06期
关键词
blood flow; electron spin resonance; hydrogen peroxide; reactive oxygen species;
D O I
10.1152/ajpheart.00515.2003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Oscillatory shear stress occurs at sites of the circulation that are vulnerable to atherosclerosis. Because oxidative stress contributes to atherosclerosis, we sought to determine whether oscillatory shear stress increases endothelial production of reactive oxygen species and to define the enzymes responsible for this phenomenon. Bovine aortic endothelial cells were exposed to static, laminar (15 dyn/cm(2)), and oscillatory shear stress (+/-15 dyn/cm(2)). Oscillatory shear increased superoxide (O2(circle-)) production by more than threefold over static and laminar conditions as detected using electron spin resonance (ESR). This increase in O-2(circle-) was inhibited by oxypurinol and culture of endothelial cells with tungsten but not by inhibitors of other enzymatic sources. Oxypurinol also prevented H2O2 production in response to oscillatory shear stress as measured by dichlorofluorescin diacetate and Amplex Red fluorescence. Xanthine-dependent O-2(circle-) production was increased in homogenates of endothelial cells exposed to oscillatory shear stress. This was associated with decreased xanthine dehydrogenase (XDH) protein levels and enzymatic activity resulting in an elevated ratio of xanthine oxidase (XO) to XDH. We also studied endothelial cells lacking the p47(phox) subunit of the NAD(P) H oxidase. These cells exhibited dramatically depressed O-2(circle-) production and had minimal XO protein and activity. Transfection of these cells with p47(phox) restored XO protein levels. Finally, in bovine aortic endothelial cells, prolonged inhibition of the NAD(P) H oxidase with apocynin decreased XO protein levels and prevented endothelial cell stimulation of O-2(circle-) production in response to oscillatory shear stress. These data suggest that the NAD(P) H oxidase maintains endothelial cell XO levels and that XO is responsible for increased reactive oxygen species production in response to oscillatory shear stress.
引用
收藏
页码:H2290 / H2297
页数:8
相关论文
共 29 条
[1]  
BECKMAN JS, 1988, J BIOL CHEM, V263, P6884
[2]  
Davies PF, 2002, BIORHEOLOGY, V39, P299
[3]   Mechanisms involved in endothelial responses to hemodynamic forces [J].
Davies, PF .
ATHEROSCLEROSIS, 1997, 131 :S15-S17
[4]   Oscillatory and steady laminar shear stress differentially affect human endothelial redox state - Role of a superoxide-producing NADH oxidase [J].
De Keulenaer, GW ;
Chappell, DC ;
Ishizaka, N ;
Nerem, RM ;
Alexander, RW ;
Griendling, KK .
CIRCULATION RESEARCH, 1998, 82 (10) :1094-1101
[5]  
Della Corte E, 1968, FEBS Lett, V2, P83, DOI 10.1016/0014-5793(68)80107-3
[7]   THE DYNAMIC-RESPONSE OF VASCULAR ENDOTHELIAL-CELLS TO FLUID SHEAR-STRESS [J].
DEWEY, CF ;
BUSSOLARI, SR ;
GIMBRONE, MA ;
DAVIES, PF .
JOURNAL OF BIOMECHANICAL ENGINEERING-TRANSACTIONS OF THE ASME, 1981, 103 (03) :177-185
[8]   Spin trapping of superoxide radicals and peroxynitrite by 1-hydroxy-3-carboxy-pyrrolidine and 1-hydroxy-2,2,6,6-tetramethyl-4-oxo-piperidine and the stability of corresponding nitroxyl radicals towards biological reductants [J].
Dikalov, S ;
Skatchkov, M ;
Bassenge, E .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 231 (03) :701-704
[9]   Transcriptional and posttranscriptional regulation of endothelial nitric oxide synthase expression by hydrogen peroxide [J].
Drummond, GR ;
Cai, H ;
Davis, ME ;
Ramasamy, S ;
Harrison, DG .
CIRCULATION RESEARCH, 2000, 86 (03) :347-354
[10]   CONVERSION OF XANTHINE DEHYDROGENASE TO OXIDASE IN ISCHEMIC RAT-TISSUES [J].
ENGERSON, TD ;
MCKELVEY, TG ;
RHYNE, DB ;
BOGGIO, EB ;
SNYDER, SJ ;
JONES, HP .
JOURNAL OF CLINICAL INVESTIGATION, 1987, 79 (06) :1564-1570