Abstract |
Viral myocarditis (VMC) is a common cardiovascular disease, and microRNAs ( miRNAs) have been postulated to be involved in its pathology. Using microarrays, we observed that miRNA-21 and -146b were upregulated in a murine model of VMC. We also found that miRNA-451 was downregulated. In vivo silencing of miRNA-21 and -146b resulted in less-severe VMC. Overexpression of miRNA-451 did not ameliorate the severity of VMC. Further work revealed that inhibition of miRNA-21 and -146b decreased the expression levels of Th17 and RORγt . Overexpression of miRNA-451 had no effect on IL-17 and RORγt expression. Inhibition of miRNA-21 and -146b might ameliorate myocardium inflammation by mediating downregulation of RORγt expression, indicating that these miRNAs are involved in the pathogenesis of murine VMC.
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Authors | Yan Li Liu, Weifeng Wu, Yimin Xue, Mengsha Gao, Yuluan Yan, Qing Kong, Yu Pang, Fan Yang |
Journal | Archives of virology
(Arch Virol)
Vol. 158
Issue 9
Pg. 1953-63
(Sep 2013)
ISSN: 1432-8798 [Electronic] Austria |
PMID | 23588407
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- MIRN146 microRNA, human
- MIRN21 microRNA, human
- MicroRNAs
- Nuclear Receptor Subfamily 1, Group F, Member 3
- Rorc protein, mouse
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Topics |
- Animals
- Cell Differentiation
(drug effects)
- Cell Line
- Coxsackievirus Infections
(genetics, physiopathology, virology)
- Disease Models, Animal
- Enterovirus B, Human
(pathogenicity)
- Gene Expression Profiling
- Humans
- Male
- Mice
- Mice, Inbred BALB C
- MicroRNAs
(genetics, metabolism, pharmacology)
- Myocarditis
(genetics, physiopathology, virology)
- Myocardium
(metabolism, pathology)
- Nuclear Receptor Subfamily 1, Group F, Member 3
- Oligonucleotide Array Sequence Analysis
- Th17 Cells
(cytology)
- Up-Regulation
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