Effects of Disturbed Flow on Vascular Endothelium: Pathophysiological Basis and Clinical Perspectives

被引:1694
作者
Chiu, Jeng-Jiann [1 ]
Chien, Shu
机构
[1] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
关键词
FLUID SHEAR-STRESS; NITRIC-OXIDE SYNTHASE; NF-KAPPA-B; LOW-DENSITY-LIPOPROTEIN; CHRONIC VENOUS INSUFFICIENCY; BONE MORPHOGENIC PROTEIN-4; SMOOTH-MUSCLE-CELLS; IN-STENT RESTENOSIS; INTERCELLULAR-ADHESION MOLECULE-1; EARLY ATHEROSCLEROTIC LESIONS;
D O I
10.1152/physrev.00047.2009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Chiu J-J, Chien S. Effects of Disturbed Flow on Vascular Endothelium: Pathophysiological Basis and Clinical Perspectives. Physiol Rev 91: 327-387, 2011; doi: 10.1152/physrev.00047.2009.-Vascular endothelial cells (ECs) are exposed to hemodynamic forces, which modulate EC functions and vascular biology/pathobiology in health and disease. The flow patterns and hemodynamic forces are not uniform in the vascular system. In straight parts of the arterial tree, blood flow is generally laminar and wall shear stress is high and directed; in branches and curvatures, blood flow is disturbed with nonuniform and irregular distribution of low wall shear stress. Sustained laminar flow with high shear stress upregulates expressions of EC genes and proteins that are protective against atherosclerosis, whereas disturbed flow with associated reciprocating, low shear stress generally upregulates the EC genes and proteins that promote atherogenesis. These findings have led to the concept that the disturbed flow pattern in branch points and curvatures causes the preferential localization of atherosclerotic lesions. Disturbed flow also results in postsurgical neointimal hyperplasia and contributes to pathophysiology of clinical conditions such as in-stent restenosis, vein bypass graft failure, and transplant vasculopathy, as well as aortic valve calcification. In the venous system, disturbed flow resulting from reflux, outflow obstruction, and/or stasis leads to venous inflammation and thrombosis, and hence the development of chronic venous diseases. Understanding of the effects of disturbed flow on ECs can provide mechanistic insights into the role of complex flow patterns in pathogenesis of vascular diseases and can help to elucidate the phenotypic and functional differences between quiescent (nonatherogenic/nonthrombogenic) and activated (atherogenic/thrombogenic) ECs. This review summarizes the current knowledge on the role of disturbed flow in EC physiology and pathophysiology, as well as its clinical implications. Such information can contribute to our understanding of the etiology of lesion development in vascular niches with disturbed flow and help to generate new approaches for therapeutic interventions.
引用
收藏
页码:327 / 387
页数:61
相关论文
共 656 条
[1]   Gene expression changes evoked in a venous segment exposed to arterial flow [J].
Abeles, Deborah ;
Kwei, Stephanie ;
Stavrakis, George ;
Zhang, Yuzhi ;
Wang, Eric T. ;
Garcia-Cardena, Guillermo .
JOURNAL OF VASCULAR SURGERY, 2006, 44 (04) :863-870
[2]   Risk factors for progression of peripheral arterial disease in large and small vessels [J].
Aboyans, Victor ;
Criqui, Michael H. ;
Denenberg, Julie O. ;
Knoke, James D. ;
Ridker, Paul M. ;
Fronek, Arnost .
CIRCULATION, 2006, 113 (22) :2623-2629
[3]   CHELATING AND FREE-RADICAL SCAVENGING MECHANISMS OF INHIBITORY-ACTION OF RUTIN AND QUERCETIN IN LIPID-PEROXIDATION [J].
AFANASEV, IB ;
DOROZHKO, AI ;
BRODSKII, AV ;
KOSTYUK, VA ;
POTAPOVITCH, AI .
BIOCHEMICAL PHARMACOLOGY, 1989, 38 (11) :1763-1769
[4]   Vascular bed-specific thrombosis [J].
Aird, W. C. .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2007, 5 :283-291
[5]   Spatial and temporal dynamics of the endothelium [J].
Aird, WC .
JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2005, 3 (07) :1392-1406
[6]   Phenotypic heterogeneity of the endothelium I. Structure, function, and mechanisms [J].
Aird, William C. .
CIRCULATION RESEARCH, 2007, 100 (02) :158-173
[7]   Phenotypic heterogeneity of the endothelium II. Representative vascular beds [J].
Aird, William C. .
CIRCULATION RESEARCH, 2007, 100 (02) :174-190
[8]   Endothelium and allotransplantation [J].
Aird, William C. .
TRANSPLANTATION, 2006, 82 (01) :S6-S8
[9]   Laminar shear stress inhibits vascular endothelial cell proliferation by inducing cyclin-dependent kinase inhibitor p21Sdi1/Cip1/Waf1 [J].
Akimoto, S ;
Mitsumata, M ;
Sasaguri, T ;
Yoshida, Y .
CIRCULATION RESEARCH, 2000, 86 (02) :185-190
[10]  
Al Suwaidi J, 2000, J AM COLL CARDIOL, V35, p63A