Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2583468 | Environmental Toxicology and Pharmacology | 2012 | 7 Pages |
Recent studies in our laboratory indicated that arsenite at 20 μM 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™ 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.
► We treated Human Umbilical Vein Endothelial Cells with arsenite. ► We found great changes in microRNAs expression after arsenic treatment. ► The alteration of miRNAs by arsenic treatment was further confirmed by qRT-PCR. ► DNA Motifs were found being existed in the promoters of the disturbed miRNAs. ► Phosphoproteins and alternative splicing proteins are targets of the miRNAs.