MicroRNA-221/222 regulate ox-LDL-induced endothelial apoptosis via Ets-1/p21 inhibition

被引:44
作者
Qin, Bing [1 ]
Cao, Yuze [2 ]
Yang, Huan [2 ]
Xiao, Bo [2 ]
Lu, Zhengqi [1 ]
机构
[1] Sun Yat Sen Univ, Dept Neurol, Affiliated Hosp 3, Guangzhou 510630, Guangdong, Peoples R China
[2] Cent S Univ, Xiangya Hosp, Dept Neurol, Changsha 410008, Hunan, Peoples R China
关键词
microRNA-221/222; HUVECs; Apoptosis; Ets-1; Atherosclerosis; TRANSCRIPTION FACTORS; COLORECTAL-CANCER; CELL APOPTOSIS; EXPRESSION; MICRORNAS; P53; ETS; ATHEROSCLEROSIS; ANGIOGENESIS; INDUCTION;
D O I
10.1007/s11010-015-2403-5
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Endothelial cells (ECs) apoptosis induced by oxidized low-density lipoprotein (ox-LDL) is thought to play an essential role in atherosclerosis. MicroRNAs (miRNAs) are a class of short non-coding RNAs, acting as posttranscriptional regulators of protein-coding genes involved in vascular cell biology. MiRNA-221 and miRNA-222 (miR-221/222) are known to be involved in the regulation of endothelial inflammation and angiogenesis. However, the function of miR-221/222 in ox-LDL-induced ECs apoptosis and atherosclerosis is still unknown. Here, we showed that miR-221/222 expression was markedly down-regulated in ox-LDL-induced apoptotic human umbilical cord vein endothelial cells. MiR-221/222 inhibition enhanced apoptosis in ECs, whereas over-expression of miR-221/222 could partly alleviate apoptotic cell death mediated by ox-LDL through suppression of Ets-1 and its downstream target p21. These findings suggest that manipulation of the miR-221/222-Ets-1-p21 pathway may offer a novel strategy for treatment of endothelial apoptosis and atherosclerosis.
引用
收藏
页码:115 / 124
页数:10
相关论文
共 35 条
[21]   Role of microRNAs in endothelial inflammation and senescence [J].
Qin, Bing ;
Yang, Huan ;
Xiao, Bo .
MOLECULAR BIOLOGY REPORTS, 2012, 39 (04) :4509-4518
[22]   MicroRNAs expression in ox-LDL treated HUVECs: MiR-365 modulates apoptosis and Bcl-2 expression [J].
Qin, Bing ;
Xiao, Bo ;
Liang, Desheng ;
Xia, Jian ;
Li, Ye ;
Yang, Huan .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 410 (01) :127-133
[23]   THE PATHOGENESIS OF ATHEROSCLEROSIS - A PERSPECTIVE FOR THE 1990S [J].
ROSS, R .
NATURE, 1993, 362 (6423) :801-809
[24]   Role of ETS family transcription factors in vascular development and angiogenesis [J].
Sato, Y .
CELL STRUCTURE AND FUNCTION, 2001, 26 (01) :19-24
[25]   ETS transcription factors and prostate cancer: The role of the family prototype ETS-1 [J].
Shaikhibrahim, Zaki ;
Wernert, Nicolas .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2012, 40 (06) :1748-1754
[26]   Dicer dependent microRNAs regulate gene expression and functions in human endothelial cells [J].
Suarez, Yajaira ;
Fernandez-Hernando, Carlos ;
Pober, Jordan S. ;
Sessa, William C. .
CIRCULATION RESEARCH, 2007, 100 (08) :1164-1173
[27]   Role of transcription factor Ets-1 in the apoptosis of human vascular endothelial cells [J].
Teruyama, K ;
Abe, M ;
Nakano, T ;
Iwasaka-Yagi, C ;
Takahashi, S ;
Yamada, S ;
Sato, Y .
JOURNAL OF CELLULAR PHYSIOLOGY, 2001, 188 (02) :243-252
[28]  
Tokarz P, 2012, ACTA BIOCHIM POL, V59, P467
[29]   MiRNA-155 targets myosin light chain kinase and modulates actin cytoskeleton organization in endothelial cells [J].
Weber, Martina ;
Kim, Sinae ;
Patterson, Nicole ;
Rooney, Kimberly ;
Searles, Charles D. .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2014, 306 (08) :H1192-H1203
[30]   Pathogenic arterial remodeling: the good and bad of microRNAs [J].
Wei, Yuanyuan ;
Schober, Andreas ;
Weber, Christian .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2013, 304 (08) :H1050-H1059