Mechanosensitive microRNAs-role in endothelial responses to shear stress and redox state

被引:100
作者
Marin, Traci [1 ]
Gongol, Brendan [1 ]
Chen, Zhen [1 ,2 ]
Woo, Brian [1 ]
Subramaniam, Shankar [3 ]
Chien, Shu [3 ]
Shyy, John Y. -J. [1 ,2 ]
机构
[1] Univ Calif Riverside, Sch Med, Riverside, CA 92521 USA
[2] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
基金
美国国家卫生研究院;
关键词
Endothelium; Shear stress; MiR; KLF2; Oxidative stress; Inflammation; Free radicals; NF-KAPPA-B; SMOOTH-MUSCLE-CELLS; THIOREDOXIN-INTERACTING PROTEIN; MANGANESE SUPEROXIDE-DISMUTASE; KRUPPEL-LIKE FACTOR-2; GENE-EXPRESSION; IN-VIVO; FLOW; INFLAMMATION; ACTIVATION;
D O I
10.1016/j.freeradbiomed.2013.05.034
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
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 Kruppel-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. (c) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:61 / 68
页数:8
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