Cell death signalling mechanisms in heart failure

被引:0
作者
Mughal, Wajihah [1 ]
Kirshenbaum, Lorrie A. [1 ]
机构
[1] Univ Manitoba, Inst Cardiovasc Sci, St Boniface Gen Hosp Res Ctr, Dept Physiol,Fac Med, Winnipeg, MB R2H 2A6, Canada
基金
加拿大健康研究院;
关键词
Apoptosis; Cell Death; Heart failure; Mitochondria; Programmed necrosis; ENDOPLASMIC-RETICULUM STRESS; UNFOLDED PROTEIN RESPONSE; MITOCHONDRIAL PERMEABILITY TRANSITION; GLYCOGEN-STORAGE-DISEASE; CYTOCHROME-C; CASPASE ACTIVATION; OXIDATIVE STRESS; BECLIN; MEDIATED APOPTOSIS; BH3-ONLY PROTEIN;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac disease is a global epidemic that is on the rise, despite the recent advances in cardiovascular research. Once the myocardium is injured, it has a limited capacity to activate reparative mechanisms to restore proper cardiac function, leading to the development of systemic heart failure. Autophagy, under certain conditions, may result in cell death, further emphasizing the controversial issues regarding the autophagic process as an adaptive or maladaptive biological response. Although significant progress in understanding the signalling mechanisms of cell death in myocytes has been made, the role of apoptotic cell death and programmed necrosis during heart failure is not completely understood. Insight to how myocytes determine whether to activate apoptotic or programmed necrosis signalling machinery remains under current investigation because it is a major problem for both scientists and clinicians in treating heart failure patients. Herein, the different modes of cell death implicated in heart failure are highlighted, as well as the role of B-cell lymphoma-2 family members and how mitochondria act as central organelles in directing such cell death mechanisms.
引用
收藏
页码:102 / 108
页数:7
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