Role of NADPH oxidases in disturbed flow- and BMP4-induced inflammation and atherosclerosis

被引:88
作者
Jo, Hanjoong
Song, Hannah
Mowbray, Amy
机构
[1] Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30332 USA
[2] Emory Univ, Div Cardiol, Atlanta, GA 30322 USA
关键词
D O I
10.1089/ars.2006.8.1609
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Atherosclerosis is an inflammatory disease, occurring preferentially in branched or curved arterial regions exposed to disturbed flow conditions including oscillatory shear stress (OS). In contrast, straight portions exposed to undisturbed laminar shear stress (LS) are relatively lesion free. The opposite effects of atheroprotective LS and proatherogenic OS are likely to be determined by differential expression of genes and proteins, including redox regulating factors. OS induces inflammation via mechanisms involving increased reactive oxygen species (ROS) production from the NADPH oxidases. Through a transcript profiling study and subsequent verification and functional studies, the authors discovered that OS induces inflammation by producing bone morphogenic protein 4 (BMP4) in endothelial cells. BMP4 stimulates expression and activity of NADPH oxidase requiring p47phox and Nox-1 in an autocrine-like manner. The NADPH oxidase activation by BMP4 then leads to ROS production, NF-kappa B activation, intercellular adhesion molecule I (ICAM-1) expression, and subsequent increased monocyte adhesivity of endothelial cells. It is proposed that endothelial NADPH oxidases play a critical role in disturbed flow- and BMP4-dependent inflammation, which is the critical early atherogenic response occurring in atheroprone areas. This emerging field of shear stress, BMP4, NADPH oxidases, inflammation, and atherosclerosis is reviewed.
引用
收藏
页码:1609 / 1619
页数:11
相关论文
共 103 条
[1]   BONE MORPHOGENETIC PROTEIN EXPRESSION IN HUMAN ATHEROSCLEROTIC LESIONS [J].
BOSTROM, K ;
WATSON, KE ;
HORN, S ;
WORTHAM, C ;
HERMAN, IM ;
DEMER, LL .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (04) :1800-1809
[2]   Gene expression profiling of human aortic endothelial cells exposed to disturbed flow and steady laminar flow [J].
Brooks, AR ;
Lelkes, PI ;
Rubanyi, GM .
PHYSIOLOGICAL GENOMICS, 2002, 9 (01) :27-41
[3]   Ductility enhancement of RC beams confined by steel cover plates [J].
Chen, CC ;
Tseng, CL .
JOURNAL OF THE CHINESE INSTITUTE OF ENGINEERS, 2001, 24 (01) :55-64
[4]  
Chen XL, 1998, CIRC RES, V83, P952
[5]   Homologs of gp91phox:: cloning and tissue expression of Nox3, Nox4, and Nox5 [J].
Cheng, GJ ;
Cao, ZH ;
Xu, XX ;
Van Meir, EG ;
Lambeth, JD .
GENE, 2001, 269 (1-2) :131-140
[6]  
CHIN JJ, 1997, ARTERIOSCLER THROMB, V17, P3570
[7]   Shear stress inhibits adhesion molecule expression in vascular endothelial cells induced by coculture with smooth muscle cells [J].
Chiu, JJ ;
Chen, LJ ;
Lee, PL ;
Lee, CI ;
Lo, LW ;
Usami, S ;
Chien, S .
BLOOD, 2003, 101 (07) :2667-2674
[8]   P-selectin or intercellular adhesion molecule (ICAM)-1 deficiency substantially protects against atherosclerosis in apolipoprotein E-deficient mice [J].
Collins, RG ;
Velji, R ;
Guevara, NV ;
Hicks, MJ ;
Chan, L ;
Beaudet, AL .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 191 (01) :189-194
[9]   Regulation of bone morphogenetic protein activity by pro domains and proprotein convertases [J].
Constam, DB ;
Robertson, EJ .
JOURNAL OF CELL BIOLOGY, 1999, 144 (01) :139-149
[10]   MINIMALLY MODIFIED LOW-DENSITY-LIPOPROTEIN INDUCES MONOCYTE CHEMOTACTIC PROTEIN-1 IN HUMAN ENDOTHELIAL-CELLS AND SMOOTH-MUSCLE CELLS [J].
CUSHING, SD ;
BERLINER, JA ;
VALENTE, AJ ;
TERRITO, MC ;
NAVAB, M ;
PARHAMI, F ;
GERRITY, R ;
SCHWARTZ, CJ ;
FOGELMAN, AM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (13) :5134-5138