Influence of TNF-α and biomechanical stress on endothelial anti- and prothrombotic genes

被引:38
作者
Bergh, N. [1 ]
Ulfhammer, E. [1 ]
Glise, K. [1 ]
Jern, S. [1 ]
Karlsson, L. [1 ]
机构
[1] Univ Gothenburg, Inst Med, Sahlgrenska Univ Hosp Ostra, Clin Expt Res Lab, SE-41685 Gothenburg, Sweden
关键词
Shear stress; Tensile stress; TNF-alpha; HUVEC; Hemostatic genes; LAMINAR SHEAR-STRESS; NECROSIS-FACTOR-ALPHA; NF-KAPPA-B; HEMODYNAMIC FORCES; IMPAIRED CAPACITY; EX-VIVO; CELLS; EXPRESSION; RESPONSES; SYSTEM;
D O I
10.1016/j.bbrc.2009.05.046
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
Biomechanical stress modulates vascular tone, vascular remodelling and the spatial localisation of atherosclerotic plaques. Inflammatory cytokines, such as TNF-alpha, regulate expression of genes that impair the function of endothelial cells. This study investigates the combinatory effect of different biomechanical stresses and TNF-alpha on the expression of endothelial anti- and prothrombotic genes. Human umbilical vein endothelial cells were exposed to TNF-alpha and different levels of static/pulsatile tensile stress or shear stress. The response in endothelial cells to TNF-a was not modulated by tensile stress. However, shear stress was a more potent stimulus. Shear stress counteracted the cytokine-induced expression of VCAM-1, and the cytokine-suppressed expression of thrombomodulin and eNOS. Shear stress and TNF-alpha additively induced PAI-1, whereas shear stress blocked the cytokine effect on t-PA and u-PA. A flow profile characterized by high laminar shear stress seems to tender the endothelial cell more resistant to inflammatory stress. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:314 / 318
页数:5
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