KLF2
机械敏感通道
细胞生物学
氧化应激
机械转化
小RNA
转录因子
内皮
炎症
平衡
机械生物学
剪应力
生物
化学
免疫学
生物化学
基因
遗传学
材料科学
受体
离子通道
复合材料
作者
Traci Marin,Brendan Gongol,Zhen Chen,Brian J. Woo,Shankar Subramaniam,Shu Chien,John Y.-J. Shyy
标识
DOI:10.1016/j.freeradbiomed.2013.05.034
摘要
Endothelial functions are highly regulated by imposed shear stress in vivo. The characteristics of shear stress determine mechanotransduction events that regulate phenotypic outcomes including redox and inflammatory states. Recent data indicate that microRNAs (miRs) in vascular endothelial cells play an essential role in shear stress-regulated endothelial responses. More specifically, atheroprotective pulsatile flow (PS) induces miRs that inhibit mediators of oxidative stress and inflammation while promoting those involved in maintaining vascular homeostasis. Conversely, oscillatory flow (OS) elicits the opposing networks. This is exemplified by the PS-responsive transcription factor Krüppel-like factor 2 (KLF2), which regulates miR expression but is also regulated by OS-sensitive miRs to ultimately regulate the oxidative and inflammatory state of the endothelium. In this review, we outline important findings demonstrating the multifaceted roles of shear stress-regulated miRs in endothelial redox and inflammatory balance. Furthermore, we discuss the use of algorithms in deciphering signaling networks differentially regulated by PS and OS.
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