TNFα induces the expression of genes associated with endothelial dysfunction through p38MAPK-mediated down-regulation of miR-149

被引:43
作者
Palmieri, Daniela [1 ]
Capponi, Simona [2 ]
Geroldi, Alessandro [2 ]
Mura, Marzia [1 ]
Mandich, Paola [2 ]
Palombo, Domenico [1 ]
机构
[1] Univ Genoa, IRCCS San Martino IST, Vasc & Endovasc Surg Unit, Res Lab Expt & Clin Vasc Biol,DISC, I-16132 Genoa, Italy
[2] Univ Genoa, IRCCS San Martino IST, Med Genet Sect, Dept Neurosci Rehabil Ophthalmol Genet & Maternal, I-16132 Genoa, Italy
关键词
MicroRNA; miR-149; TNF alpha; Endothelial dysfunction; MMP-9; iNOS; IL-6; MICRORNA; APOPTOSIS; DISEASES;
D O I
10.1016/j.bbrc.2013.11.092
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 have been proposed as novel regulators of vascular inflammation and dysfunction. This study aimed to evaluate the role of miR-149 in regulating the expression of key molecules associated with TNF alpha-induced endothelial activation. miR-149 was selected by in silico analysis and microRNA target prediction. Endothelial dysfunction was induced by TNF alpha treatment in Eahy926 endothelial cells and HUVEC. miR-149 level was evaluated by quantitative real time-polymerase chain reaction (RT-qPCR). Metalloproteinase-9 (MMP-9) was measured by zymography, Inducible Nitric Oxide Synthase (iNOS) by immunoblotting, Interleukin-6 (IL-6) and Interleukin-8 (IL-8) by ELISA. miR-149 regulatory effect was evaluated by gain-of-function technique upon miR-149 mimics transfection. TNF alpha down-modulated miR-149 level in Eahy926 and HUVEC. This effect was significantly abolished in Eahy926 by treatment with p38MAPK inhibitor. miR-149 mimic transfection counteracted the TNF alpha-induced expression of MMP-9, iNOS and IL-6. No effect was detected on IL-8 expression. Our results suggest that miR-149 represents an important new regulator of endothelial function through negative regulation of molecules associated with TNF alpha-induced endothelial dysfunction. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:246 / 251
页数:6
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