Partial carotid ligation is a model of acutely induced disturbed flow, leading to rapid endothelial dysfunction and atherosclerosis

被引:397
作者
Nam, Douglas [2 ]
Ni, Chih-Wen [3 ]
Rezvan, Amir [2 ]
Suo, Jin [3 ]
Budzyn, Klaudia [2 ]
Llanos, Alexander [2 ]
Harrison, David [2 ]
Giddens, Don [3 ]
Jo, Hanjoong [1 ,2 ,3 ,4 ]
机构
[1] Emory Univ, Coulter Dept Biomed Engn, Atlanta, GA 30322 USA
[2] Emory Univ, Dept Med, Div Cardiol, Atlanta, GA 30322 USA
[3] Georgia Tech, Coulter Dept Biomed Engn, Atlanta, GA 30322 USA
[4] Ewha Womans Univ, Dept Bioinspired Sci, Seoul, South Korea
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2009年 / 297卷 / 04期
关键词
shear stress; endothelial dysfunction; inflammation; atherosclerosis; endothelium; BONE MORPHOGENIC PROTEIN-4; NITRIC-OXIDE SYNTHASE; FLUID SHEAR-STRESS; E-DEFICIENT MICE; NADPH OXIDASES; MOUSE AORTAS; IN-VITRO; EXPRESSION; CELLS; INFLAMMATION;
D O I
10.1152/ajpheart.00510.2009
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Nam D, Ni CW, Rezvan A, Suo J, Budzyn K, Llanos A, Harrison D, Giddens D, Jo H. Partial carotid ligation is a model of acutely induced disturbed flow, leading to rapid endothelial dysfunction and atherosclerosis. Am J Physiol Heart Circ Physiol 297: H1535-H1543, 2009. First published August 14, 2009; doi: 10.1152/ajpheart.00510.2009.-Atherosclerosis is closely associated with disturbed flow characterized by low and oscillatory shear stress, but studies directly linking disturbed flow to atherogenesis is lacking. The major reason for this has been a lack of an animal model in which disturbed flow can be acutely induced and cause atherosclerosis. Here, we characterize partial carotid ligation as a model of disturbed flow with characteristics of low and oscillatory wall shear stress. We also describe a method of isolating intimal RNA in sufficient quantity from mouse carotid arteries. Using this model and method, we found that partial ligation causes upregulation of proatherogenic genes, downregulation of antiatherogenic genes, endothelial dysfunction, and rapid atherosclerosis in 2 wk in a p47(phox)-dependent manner and advanced lesions by 4 wk. We found that partial ligation results in endothelial dysfunction, rapid atherosclerosis, and advanced lesion development in a physiologically relevant model of disturbed flow. It also allows for easy and rapid intimal RNA isolation. This novel model and method could be used for genome-wide studies to determine molecular mechanisms underlying flow-dependent regulation of vascular biology and diseases.
引用
收藏
页码:H1535 / H1543
页数:9
相关论文
共 39 条
[1]  
Barry-Lane PA, 2001, J CLIN INVEST, V108, P1513, DOI 10.1172/JCI200111927
[2]   Atheroprotective signaling mechanisms activated by steady laminar flow in endothelial cells [J].
Berk, Bradford C. .
CIRCULATION, 2008, 117 (08) :1082-1089
[3]   Bone morphogenic protein antagonists are coexpressed with bone morphogenic protein 4 in endothelial cells exposed to unstable flow in vitro in mouse aortas and in human coronary arteries - Role of bone morphogenic protein antagonists in inflammation and atherosclerosis [J].
Chang, Kyunghwa ;
Weiss, Daiana ;
Suo, Jin ;
Vega, J. David ;
Giddens, Don ;
Taylor, W. Robert ;
Jo, Hanjoong .
CIRCULATION, 2007, 116 (11) :1258-1266
[4]   Oscillatory shear stress stimulates adhesion molecule expression in cultured human endothelium [J].
Chappell, DC ;
Varner, SE ;
Nerem, RM ;
Medford, RM ;
Alexander, RW .
CIRCULATION RESEARCH, 1998, 82 (05) :532-539
[5]   Role of endothelial shear stress in the natural history of coronary atherosclerosis and vascular remodeling - Molecular, cellular, and vascular behavior [J].
Chatzizisis, Yiannis S. ;
Coskun, Ahmet Umit ;
Jonas, Michael ;
Edelman, Elazer R. ;
Feldman, Charles L. ;
Stone, Peter H. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2007, 49 (25) :2379-2393
[6]  
CHENG C, 2005, BLOOD
[7]   Atherosclerotic lesion size and vulnerability are determined by patterns of fluid shear stress [J].
Cheng, Caroline ;
Tempel, Dennie ;
van Haperen, Rien ;
van der Baan, Arjen ;
Grosveld, Frank ;
Daemen, Mat J. A. P. ;
Krams, Rob ;
de Crom, Rini .
CIRCULATION, 2006, 113 (23) :2744-2753
[8]   Mechanism of endothelial dysfunction in apolipoprotein E-deficient mice [J].
d'Uscio, LV ;
Baker, TA ;
Mantilla, CB ;
Smith, L ;
Weiler, D ;
Sieck, GC ;
Katusic, ZS .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2001, 21 (06) :1017-1022
[9]   Distinct endothelial phenotypes evoked by arterial waveforms derived from atherosclerosis-susceptible and -resistant regions of human vasculature [J].
Dai, GH ;
Kaazempur-Mofrad, MR ;
Natarajan, S ;
Zhang, YZ ;
Vaughn, S ;
Blackman, BR ;
Kamm, RD ;
García-Cardeña, G ;
Gimbrone, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (41) :14871-14876
[10]   FLOW-MEDIATED ENDOTHELIAL MECHANOTRANSDUCTION [J].
DAVIES, PF .
PHYSIOLOGICAL REVIEWS, 1995, 75 (03) :519-560