Endothelial MicroRNAs and Atherosclerosis

被引:119
作者
Sun, Xinghui [1 ]
Belkin, Nathan [1 ]
Feinberg, Mark W. [1 ]
机构
[1] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Cardiovasc,Dept Med, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
MicroRNA; MiR-181b; Vascular inflammation; Atherosclerosis; Endothelial activation; Nuclear factor kappa B; NF-KAPPA-B; TYPE-1 RECEPTOR EXPRESSION; EMBRYONIC STEM-CELLS; APOE-DEFICIENT MICE; SHEAR-STRESS; IN-VITRO; VASCULAR INFLAMMATION; HUMAN FIBROBLASTS; DISTURBED FLOW; CYCLIN D1;
D O I
10.1007/s11883-013-0372-2
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
The vascular endothelium, a thin layer of endothelial cells (ECs) that line the inner surface of blood vessels, is a critical interface between blood and all tissues. EC activation, dysfunction, and vascular inflammation occur when the endothelium is exposed to various insults such as proinflammatory cytokines, oxidative stress, hypertension, hyperglycemia, aging, and shear stress. These insults lead to the pathogenesis of a range of disease states, including atherosclerosis. Several signaling pathways, especially nuclear factor kappa B mediated signaling, play crucial roles in these pathophysiological processes. Recently, microRNAs (miRNAs) have emerged as important regulators of EC function by fine-tuning gene expression. In this review, we discuss how miRNAs regulate EC function and vascular inflammation in response to a variety of pathophysiologic stimuli. An understanding of the role of miRNAs in EC activation and dysfunction may provide novel targets and therapeutic opportunities for controlling atherosclerosis and other chronic inflammatory disease states.
引用
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页数:13
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