Notch1 protects against myocardial ischaemia-reperfusion injury via regulating mitochondrial fusion and function

被引:31
|
作者
Dai, Shao-hua [1 ]
Wu, Qi-cai [1 ]
Zhu, Rong-rong [2 ]
Wan, Xue-mei [1 ]
Zhou, Xue-liang [1 ]
机构
[1] Nanchang Univ, Dept Cardiovasc Surg, Affiliated Hosp 1, Nanchang 330006, Jiangxi, Peoples R China
[2] Nanchang Univ, Dept Obstet & Gynecol, High Tech Hosp, Affiliated Hosp 1, Nanchang 330096, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
DRP1; MFN1; mitochondrial fusion; myocardial ischaemic reperfusion; Notch1; MOUSE HEARTS; FISSION;
D O I
10.1111/jcmm.14992
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitochondrial fusion and fission dynamic are critical to the myocardial protection against ischaemia-reperfusion injury. Notch1 signalling plays an important role in heart development, maturation and repair. However, the role of Notch1 in the myocardial mitochondrial fusion and fission dynamic remains elusive. Here, we isolated myocardial cells from rats and established myocardial ischaemia-reperfusion injury (IRI) model. We modulated Notch1, MFN1 and DRP1 expression levels in myocardial cells via infection with recombinant adenoviruses. The results showed that Notch1 improves the cell viability and mitochondrial fusion in myocardiocytes exposed to IRI. These improvements were dependent on the regulation of MFN1 and DRP1. On the mechanism, we found that MNF1 is transcriptionally activated by RBP-Jk in myocardiocytes. Notch1 also improves the mitochondrial membrane potential in myocardiocytes exposed to IRI. Moreover, we further confirmed the protection of the Notch1-MFN1/Drp1 axis on the post-ischaemic recovery of myocardial performance is associated with the preservation of the mitochondrial structure. In conclusion, this study presented a detailed mechanism by which Notch1 signalling improves mitochondrial fusion during myocardial protection.
引用
收藏
页码:3183 / 3191
页数:9
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