Abstract | OBJECTIVE: MATERIALS AND METHODS: The rat model of MI was successfully established in-vivo. MiR-548c-3p was upregulated via lentivirus transfection with miR-548c-3p mimics. Cardiac function of rats was detected via echocardiography. Meanwhile, Sirius red and Masson staining were used to detect the level of fibrosis index in MI model. Subsequently, myocardial fibroblasts were isolated and cultured in vitro. An oxygen- glucose deprivation (OGD) model was established to mimicking the ischemic condition. Furthermore, the relationship between miR-548c-3p and c-Myb was verified, and the levels of fibrosis-related factors (including α-SMA and COL1A1) were measured. RESULTS: In-vivo experiments showed that miR-548c-3p expression in rats was significantly down-regulated at 2 and 4 weeks after MI. Up-regulation of miR-548c-3p significantly improved cardiac function, reduced myocardial fibrosis and inhibited the protein expression of proto-oncogene c-Myb (c-Myb). In vitro experiments revealed that c-Myb was a target gene of miR-548c-3p. In addition, miR-548c-3p could inhibit the expressions of α-SMA and COL1A1 through targeting c-Myb. CONCLUSIONS: MiR-548c-3p could improve myocardial fibrosis by targeting c-Myb.
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Authors | L-X Zhang, S-H Zhang, C-Q Wang, Q Bing, Z Zhao, J Wang, L Zhang |
Journal | European review for medical and pharmacological sciences
(Eur Rev Med Pharmacol Sci)
Vol. 23
Issue 11
Pg. 4908-4916
(Jun 2019)
ISSN: 2284-0729 [Electronic] Italy |
PMID | 31210326
(Publication Type: Journal Article)
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Chemical References |
- Acta2 protein, rat
- Actins
- Collagen Type I
- Collagen Type I, alpha 1 Chain
- MAS1 protein, human
- MIRN548c microRNA, rat
- MicroRNAs
- Proto-Oncogene Mas
- Proto-Oncogene Proteins c-myb
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Topics |
- Actins
(metabolism)
- Animals
- Apoptosis
(genetics)
- Cells, Cultured
- Collagen Type I
(metabolism)
- Collagen Type I, alpha 1 Chain
- Disease Models, Animal
- Down-Regulation
- Fibroblasts
- Fibrosis
- Humans
- Male
- MicroRNAs
(metabolism)
- Myocardial Infarction
(genetics, pathology)
- Myocardium
(pathology)
- Primary Cell Culture
- Proto-Oncogene Mas
- Proto-Oncogene Proteins c-myb
(genetics)
- Rats
- Rats, Sprague-Dawley
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