Adaptive response of vascular endothelial cells to an acute increase in shear stress frequency

被引:22
作者
Zhang, Ji [1 ]
Friedman, Morton H. [1 ,2 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27706 USA
[2] George Washington Univ, Dept Mech & Aerosp Engn, Washington, DC 20052 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2013年 / 305卷 / 06期
关键词
endothelial permeability; gene expression; adaptation; shear stress; frequency; PERMEABILITY; FLOW; PROLIFERATION; EXPRESSION; ID2; ANGIOGENESIS; GRADIENT; FORCES; NUSAP;
D O I
10.1152/ajpheart.00174.2013
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Local shear stress sensed by arterial endothelial cells is occasionally altered by changes in global hemodynamic parameters, e.g., heart rate and blood flow rate, as a result of normal physiological events, such as exercise. In a recently study (41), we demonstrated that during the adaptive response to increased shear magnitude, porcine endothelial cells exhibited an unique phenotype featuring a transient increase in permeability and the upregulation of a set of anti-inflammatory and antioxidative genes. In the present study, we characterize the adaptive response of these cells to an increase in shear frequency, another important hemodynamic parameter with implications in atherogenesis. Endothelial cells were preconditioned by a basal-level sinusoidal shear stress of 15 +/- 15 dyn/cm(2) at 1 Hz, and the frequency was then elevated to 2 Hz. Endothelial permeability increased slowly after the frequency step-up, but the increase was relatively small. Using microarrays, we identified 37 genes that are sensitive to the frequency step-up. The acute increase in shear frequency upregulates a set of cell-cycle regulation and angiogenesis-related genes. The overall adaptive response to the increased frequency is distinctly different from that to a magnitude step-up. However, consistent with the previous study, our data support the notion that endothelial function during an adaptive response is different than that of fully adapted endothelial cells. Our studies may also provide insights into the beneficial effects of exercise on vascular health: transient increases in frequency may facilitate endothelial repair, whereas similar increases in shear magnitude may keep excessive inflammation and oxidative stress at bay.
引用
收藏
页码:H894 / H902
页数:9
相关论文
共 41 条
[1]   Temporal gradient in shear but not steady shear stress induces PDGF-A and MCP-1 expression in endothelial cells -: Role of NO, NFκB, and egr-1 [J].
Bao, XP ;
Lu, CY ;
Frangos, JA .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (04) :996-1003
[2]   Role of Id proteins in embryonic and tumor angiogenesis [J].
Benezra, R .
TRENDS IN CARDIOVASCULAR MEDICINE, 2001, 11 (06) :237-241
[3]   Biological roles of fibroblast growth factor-2 [J].
Bikfalvi, A ;
Klein, S ;
Pintucci, G ;
Rifkin, DB .
ENDOCRINE REVIEWS, 1997, 18 (01) :26-45
[4]  
Chien S, 2006, BIORHEOLOGY, V43, P95
[5]   Effects of disturbed flow on endothelial cells [J].
Chien, Shu .
ANNALS OF BIOMEDICAL ENGINEERING, 2008, 36 (04) :554-562
[6]   Regulation of bovine brain microvascular endothelial tight junction assembly and barrier function by laminar shear stress [J].
Colgan, Olga C. ;
Ferguson, Gail ;
Collins, Nora T. ;
Murphy, Ronan P. ;
Meade, Gerardeane ;
Cahill, Paul A. ;
Cummins, Philip M. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2007, 292 (06) :H3190-H3197
[7]   Id2 Promotes Tumor Cell Migration and Invasion through Transcriptional Repression of Semaphorin 3F [J].
Coma, Silvia ;
Amin, Dhara N. ;
Shimizu, Akio ;
Lasorella, Anna ;
Iavarone, Antonio ;
Klagsbrun, Michael .
CANCER RESEARCH, 2010, 70 (09) :3823-3832
[8]   The G2 DNA damage checkpoint delays expression of genes encoding mitotic regulators [J].
Crawford, DF ;
Piwnica-Worms, H .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (40) :37166-37177
[9]   The role of shear stress in the pathogenesis of atherosclerosis [J].
Cunningham, KS ;
Gotlieb, AI .
LABORATORY INVESTIGATION, 2005, 85 (01) :9-23
[10]   MOLECULAR MECHANISMS OF ANGIOGENESIS - FIBROBLAST GROWTH-FACTOR SIGNAL-TRANSDUCTION [J].
FRIESEL, RE ;
MACIAG, T .
FASEB JOURNAL, 1995, 9 (10) :919-925