Abstract | AIM: This study was conducted to investigate the role of the miR-210/Caspase8ap2 pathway in apoptosis and autophagy in hypoxic myocardial cells. METHODS: The miR-control, miR-210 mimic, and miR-210 inhibitor were transfected into rat myocardial H9C2 cells. The transfection efficiency of exogenous miR-210 was determined by quantitative reverse-transcription polymerase chain reaction (qRT-PCR). H9C2 cells were then treated with CoCl2 for 24, 48, and 72 h to generate a myocardial injury model. The apoptosis of H9C2 cells was assessed by flow cytometry. Additionally, a western blot assay was used to determine the expression of the autophagy-associated proteins light chain 3 (LC3), p62 and Beclin-1, and apoptosis-associated proteins Caspase8ap2, cleaved caspase 8, and cleaved caspase 3. RESULTS: We determined that a 48 h hypoxia treatment duration in H9C2 cardiomyocytes induced myocardial injury. Additionally, the overexpression of miR-210 significantly inhibited cell apoptosis. MiR-210 suppressed autophagy by upregulating p62 and downregulating LC3II/I in hypoxic H9C2 cells. Caspase8ap2 was a putative target of miR-210, miR-210 mediated apoptosis, and autophagy of H9C2 cells via suppressing Caspase8ap2. Furthermore, the expression of caspase 8, caspase 3, and Beclin-1 were decreased in response to miR-210. CONCLUSION: miR-210 exhibits anti-apoptosis and anti-autophagy effects, which alleviate myocardial injury in response to hypoxia.
|
Authors | Kunsheng Li, Jun Pan, Qiuchang Li, Shiliang Li, Kai Li, Yongqing Cheng, Lin Chai, Chao Li, Junling Li, Zhikun Fu, Dongjin Wang, Yang Bai |
Journal | The heart surgery forum
(Heart Surg Forum)
Vol. 23
Issue 6
Pg. E797-E802
(Oct 21 2020)
ISSN: 1522-6662 [Electronic] United States |
PMID | 33234216
(Publication Type: Journal Article)
|
Chemical References |
- Apoptosis Regulatory Proteins
- CASP8AP2 protein, rat
- MIRN210 microRNA, rat
- MicroRNAs
|
Topics |
- Animals
- Apoptosis
- Apoptosis Regulatory Proteins
(biosynthesis, genetics)
- Autophagy
- Blotting, Western
- Cell Line
- Disease Models, Animal
- Gene Expression Regulation
- MicroRNAs
(biosynthesis, genetics)
- Myocardial Reperfusion Injury
(genetics, metabolism, pathology)
- Myocytes, Cardiac
(metabolism, pathology)
- Rats
- Signal Transduction
|