Programmed Necrosis, Not Apoptosis, in the Heart

被引:228
作者
Kung, Gloria
Konstantinidis, Klitos
Kitsis, Richard N. [1 ]
机构
[1] Albert Einstein Coll Med, Wilf Family Cardiovasc Res Inst, Bronx, NY 10461 USA
关键词
cell death; necrosis; apoptosis; myocardial infarction; heart failure; MITOCHONDRIAL PERMEABILITY TRANSITION; NECROTIC CELL-DEATH; ADENINE-NUCLEOTIDE TRANSLOCASE; LYSOSOMAL MEMBRANE PERMEABILIZATION; ISCHEMIA-REPERFUSION INJURY; ACUTE MYOCARDIAL-INFARCTION; ENDOPLASMIC-RETICULUM CA2+; ELECTRON-TRANSPORT CHAIN; C-EPSILON INTERACTS; FAILING HUMAN HEART;
D O I
10.1161/CIRCRESAHA.110.225730
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
It is well known that apoptosis is an actively mediated cell suicide process. In contrast, necrosis, a morphologically distinct form of cell death, has traditionally been regarded as passive and unregulated. Over the past decade, however, experiments in Caenorhabditis elegans and mammalian cells have revealed that a significant proportion of necrotic death is, in fact, actively mediated by the doomed cell. Although a comprehensive understanding of necrosis is still lacking, some key molecular events have come into focus. Cardiac myocyte apoptosis and necrosis are prominent features of the major cardiac syndromes. Accordingly, the recognition of necrosis as a regulated process mandates a reexamination of cell death in the heart. This review discusses pathways that mediate programmed necrosis, how they intersect with apoptotic pathways, roles of necrosis in heart disease, and new therapeutic opportunities that the regulated nature of necrosis presents. (Circ Res. 2011;108:1017-1036.)
引用
收藏
页码:1017 / 1036
页数:20
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