The integrin-mediated cyclic strain-induced signaling pathway in vascular endothelial cells.

S. Frangos, R. Knox, Y. Yano, E. Chen, G. Di Luozzo, A. H. Chen, B. Sumpio
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引用次数: 30

Abstract

The irregular distribution of plaque in the vasculature results from the interaction of local hemodynamic forces with the vessel wall. One well-characterized force is cyclic circumferential strain, the repetitive pulsatile pressure distention on the arterial wall. This review summarizes current research, which has aimed to elicit the signal transduction pathway by which cyclic strain elicits functional and structural responses in endothelial cells; specifically, it summarizes the signaling pathway that begins with the reorganization of integrins. One method by which these extracellular matrix receptors affect signal transduction is through their ability to initiate the process of phosphorylation on tyrosine residues of cytoplasmic protein kinases, including focal adhesion kinase. The strain-induced pathway appears to also involve ras and the mitogen-activated protein kinase family of enzymes, and preliminary data suggests a role for src as well. Ultimately, it is the regulation of gene expression through the modulation of transcription factors that allows endothelial cells to respond to changes in local hemodynamics.
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血管内皮细胞中整合素介导的循环菌株诱导的信号通路。
斑块在血管中的不规则分布是局部血流动力学力与血管壁相互作用的结果。一种很好表征的力是循环周向应变,即动脉壁上的重复脉动压力扩张。本文综述了目前的研究,旨在引出循环应变引起内皮细胞功能和结构反应的信号转导途径;具体来说,它总结了从整合素重组开始的信号通路。这些细胞外基质受体影响信号转导的一种方法是通过它们启动细胞质蛋白激酶酪氨酸残基磷酸化过程的能力,包括局灶黏附激酶。菌株诱导的途径似乎也涉及ras和丝裂原激活蛋白激酶家族的酶,初步数据表明src也起作用。最终,正是通过转录因子的调节来调节基因表达,使得内皮细胞能够对局部血流动力学的变化做出反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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