The role of miRNA-29b1 on the hypoxia-induced apoptosis in mammalian cardiomyocytes

被引:0
|
作者
Dai, Bo [1 ,2 ]
Liu, Hailin [1 ]
Juan, Dingmin [1 ]
Wu, Kaize [1 ]
Cao, Ruhao [1 ]
机构
[1] South China Univ Technol, Affiliated Hosp 6, Sch Med, Dept Cardiol, Foshan, Peoples R China
[2] South China Univ Technol, Affiliated Hosp 6, Sch Med, Dept Cardiol, 120 Guidan Rd, Foshan 528200, Guangdong, Peoples R China
来源
EUROPEAN JOURNAL OF HISTOCHEMISTRY | 2024年 / 68卷 / 03期
基金
中国国家自然科学基金;
关键词
hypoxia; cardiomyocyte; apoptosis; miR-29b1; Cx43; CELL-DEATH; GAP-JUNCTION; CYTOCHROME-C; ISCHEMIC-STROKE; MITOCHONDRIA; INHIBITION; ACTIVATION; MICRORNAS; MYOCYTES; THERAPY;
D O I
10.4081/ejh.2024.4021
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cardiomyocyte apoptosis is a complex biological process involving the interaction of many factors and signaling pathways. In hypoxic environment, cardiomyocytes may trigger apoptosis due to insufficient energy supply, increased production of oxygen free radicals, and disturbance of intracellular calcium ion balance. The present research aimed to investigate the role of microRNA-29b1 (miR-29b1) in hypoxia-treated cardiomyocytes and its potential mechanism involved. We established an in vitro ischemia model using AC16 and H9C2 cardiomyocytes through hypoxia treatment (1% O2, 48 h). Cell apoptosis was evaluated by flow cytometry using Annexin V-FITC-PI staining assay. Moreover, we used Western blot and immunofluorescence analysis to determine the expression of Bcl-2, Bax, caspase-3 and Cx43 proteins. We found that miR-29b1 protected AC16 and H9C2 cells from hypoxia-induced injury as evidence that miR-29b1 attenuated the effects of hypoxia treatment on AC16 and H9C2 cell apoptosis after hypoxia treatment. In conclusion, our findings suggest that miR-29b1 may have potential cardiovascular protective effects during ischemia-related myocardial injury.
引用
收藏
页数:9
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