Altered expression profiles of microRNAs upon arsenic exposure of human umbilical vein endothelial cells

被引:22
|
作者
Li, Xinna [1 ]
Shi, Yanfen [1 ]
Wei, Yudan [2 ]
Ma, Xiaotu [3 ]
Li, Yulin [1 ]
Li, Ronggui [1 ]
机构
[1] Jilin Univ, Key Lab Pathobiol, Minist Educ, Norman Bethune Coll Med, Changchun 130021, Peoples R China
[2] Mercer Univ, Sch Med, Dept Community Med, Macon, GA 31207 USA
[3] Univ Texas Dallas, Dept Mol & Cell Biol, Ctr Syst Biol, Richardson, TX 75083 USA
基金
中国国家自然科学基金;
关键词
Arsenic; microRNAs; HUVECs; DNA motifs; TRIOXIDE TREATMENT; BLACKFOOT DISEASE; POLYMERASE-II; TAIWAN; CANCER; GROUNDWATER; P53;
D O I
10.1016/j.etap.2012.05.003
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Recent studies in our laboratory indicated that arsenite at 20 mu M significantly induces the apoptosis of HUVECs. In this study we analyzed miRNAs expression profiles upon arsenic exposure of these cells to explore the molecular mechanisms of arsenic-induced vascular toxicity. The expression of miRNAs was examined by Exiqon miRCURY (TM) LNA microRNA chips. We found that 85 miRNAs were up-regulated and 52 were down-regulated by arsenic treatment as compared to the control group. The expression of altered miRNAs was validated by quantitative reverse-transcription PCR (qRT-PCR). A number of DNA motifs were identified in the promoters of the perturbed miRNAs by promoter analysis using MEME software. Analysis of cellular functions by using DAVID Bioinformatics Resources revealed that phosphoproteins and genes involved in alternative splicing are among the top categories targeted by both up- and down-regulated miRNAs. In conclusion, the results show that the alteration of miRNAs expression might play crucial roles in arsenic-induced vascular injury. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:381 / 387
页数:7
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