Programmed cardiomyocyte death in myocardial infarction

被引:4
作者
Wu, Hao [1 ]
Lan, Qi [1 ]
He, Yi-Xiang [1 ]
Xue, Jin-Yi [1 ]
Liu, Hao [2 ]
Zou, Yuan [1 ]
Liu, Ping [1 ]
Luo, Gang [1 ]
Chen, Ming-Tai [3 ]
Liu, Meng-Nan [1 ]
机构
[1] Southwest Med Univ, Affiliated Tradit Chinese Med Hosp, Natl Tradit Chinese Med Clin Res Base, Luzhou 646000, Sichuan, Peoples R China
[2] Southwest Med Univ, Affiliated Hosp, Dept Pediat, Luzhou 646000, Sichuan, Peoples R China
[3] Guangzhou Univ Chinese Med, Shenzhen Tradit Chinese Med Hosp, Shenzhen 518033, Peoples R China
关键词
Cardiovascular disease; Myocardial infarction; Cardiomyocytes; Cardiac repair; Programmed cell death; CELL-DEATH; EXTRACELLULAR VESICLES; NLRP3; INFLAMMASOME; CARDIAC-FUNCTION; GROWTH-FACTOR; APOPTOSIS; AUTOPHAGY; HEART; KINASE; FERROPTOSIS;
D O I
10.1007/s10495-025-02075-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cardiovascular disease (CVD) is a leading cause of human mortality worldwide, with patients often at high risk of heart failure (HF) in myocardial infarction (MI), a common form of CVD that results in cardiomyocyte death and myocardial necrosis due to inadequate myocardial perfusion. As terminally differentiated cells, cardiomyocytes possess a severely limited capacity for regeneration, and an excess of dead cardiomyocytes will further stress surviving cells, potentially exacerbating to more extensive heart disease. The article focuses on the relationship between programmed cell death (PCD) of cardiomyocytes, including different forms of apoptosis, necrosis, and autophagy, and MI, as well as the potential application of these mechanisms in the treatment of MI. By gaining a deeper understanding of the mechanisms of cardiomyocyte death, it aims to provide new insights into the prevention and treatment of MI.
引用
收藏
页码:597 / 615
页数:19
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