| Literature DB >> 24863965 |
Cheng-Shyuan Rau1, Johnson Chia-Shen Yang2, Yi-Chun Chen2, Chia-Jung Wu2, Tsu-Hsiang Lu2, Siou-Ling Tzeng2, Yi-Chan Wu2, Ching-Hua Hsieh3.
Abstract
This aim of this study was to explore the role of miRNA-146a (miR-146a) and its target genes in endothelial cells. We demonstrated that lipopolysaccharide (LPS) induced the upregulation of miR-146a in human umbilical vein endothelial cells (HUVECs), and that the induction was blocked by silencing toll-like receptors, the adaptor molecule MyD88, and the nonspecific NF-κB inhibitor BAY 11-7082. In addition, knockdown of miR-146a by transfection of the locked nucleic acid antimiR-146a significantly inhibited LPS-induced cell migration and tube formation. A combined analysis of bioinformatics miRanda algorithms and a whole genome expression microarray of immunoprecipitated Ago2 ribonucleoprotein complexes identified 14 potential target genes. Subsequent transfection with the miR-146a precursor pre-miR-146a into HUVECs validated that CARD10 was the target gene of the miR-146a, both at the mRNA and protein levels. Silencing CARD10 inhibited p65 nuclear translocation in the cells receiving LPS stimulation and increased angiogenesis. Therefore, miR-146a may play a role in regulating the angiogenesis in HUVECs by downregulating CARD10, which acts in a negative feedback regulation loop to inhibit the activation of NF-κB that normally impairs angiogenesis.Entities:
Keywords: Ago2; CARD10; lipopolysaccharide (LPS); miR-146a; nuclear factor-κB (NF-κB); whole genome microarray
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Year: 2014 PMID: 24863965 DOI: 10.1093/toxsci/kfu097
Source DB: PubMed Journal: Toxicol Sci ISSN: 1096-0929 Impact factor: 4.849