miR-125a-5p Modulates Phenotypic Switch of Vascular Smooth Muscle Cells by Targeting ETS-1

被引:48
|
作者
Gareri, C. [1 ,3 ]
Iaconetti, C. [1 ]
Sorrentino, S. [1 ]
Covello, C. [1 ]
De Rosa, S. [1 ]
Indolfi, C. [1 ,2 ]
机构
[1] Magna Graecia Univ Catanzaro, Div Cardiol, Dept Med & Surg Sci, Viale Europa, I-88100 Catanzaro, Italy
[2] CNR, IFC, URT, Dept Med, Catanzaro, Italy
[3] Duke Univ, Dept Med, Durham, NC 27710 USA
关键词
microRNAs; vascular smooth muscle cells; ETS-1; restenosis; CORONARY-STENT PLACEMENT; BARE-METAL STENTS; ANGIOGRAPHIC PATTERNS; MOLECULAR-MECHANISMS; ELUTING STENTS; BALLOON INJURY; LUNG-CANCER; IN-VIVO; MICRORNAS; RESTENOSIS;
D O I
10.1016/j.jmb.2017.05.008
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
MicroRNAs are key regulators of vascular smooth muscle cells (VSMCs) phenotypic switch, one of the main events responsible for bare metal in-stent restenosis after percutaneous coronary intervention. miR-125a-5p is an important modulator of differentiation, proliferation, and migration in different cell types; however, its role in VSMCs is still unknown. The aim of this study was to evaluate the role of miR-125a-5p in VSMCs phenotypic switch. Our results suggest that miR-125a-5p is highly expressed in VSMCs, but it is down regulated after vascular injury in vivo. Its overexpression is sufficient to reduce VSMCs proliferation and migration, and it is able to promote the expression of selective VSMCs markers such as alpha smooth muscle actin, myosin heavy chain 11, and smooth muscle 22 alpha. Interestingly, miR-125a-5p directly targets ETS-1, a transcription factor implicated in cell proliferation and migration and is crucial in PDGF-BB pathway in VSMCs. Thus, miR-125a-5p in this context inhibits PDGF-BB pathway and is therefore a potential regulator of VSMCs phenotypic switch. (C) 2017 Published by Elsevier Ltd.
引用
收藏
页码:1817 / 1828
页数:12
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