Two Close, Too Close Sarcoplasmic Reticulum-Mitochondrial Crosstalk and Cardiomyocyte Fate

被引:58
作者
Dorn, Gerald W., II [1 ]
Scorrano, Luca [2 ,3 ]
机构
[1] Washington Univ, Ctr Pharmacogenom, Dept Internal Med, Sch Med, St Louis, MO 63110 USA
[2] Univ Geneva, Sch Med, Dept Cell Physiol & Metab, CH-1206 Geneva, Switzerland
[3] Venetian Inst Mol Med, Dulbecco Telethon Inst, Padua, Italy
基金
瑞士国家科学基金会;
关键词
mitochondrial fusion; endoplasmic reticulum; calcium; apoptosis; mitochondrial permeability transition; PERMEABILITY TRANSITION PORE; ADENINE-NUCLEOTIDE TRANSLOCATOR; DEPENDENT PROTEIN-KINASE; APOPTOTIC CELL-DEATH; ENDOPLASMIC-RETICULUM; CYCLOPHILIN-D; CYTOCHROME-C; CARDIAC-HYPERTROPHY; HEART-FAILURE; DILATED CARDIOMYOPATHY;
D O I
10.1161/CIRCRESAHA.110.225714
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Mitochondria are key organelles in cell life whose dysfunction is associated with a variety of diseases. Their crucial role in intermediary metabolism and energy conversion makes them a preferred target in tissues, such as the heart, where the energetic demands are very high. In the cardiomyocyte, the spatial organization of mitochondria favors their interaction with the sarcoplasmic reticulum, thereby offering a mechanism for Ca2+-mediated crosstalk between these 2 organelles. Recently, the molecular basis for this interaction has begun to be unraveled, and we are learning how endoplasmic reticulum-mitochondrial interactions are often exploited by death signals, such as proapoptotic Bcl-2 family members, to amplify the cell death cascade. Here, we review our present understanding of the structural basis and the functional consequences of the close interaction between sarcoplasmic reticulum and mitochondria on cardiomyocyte function and death. (Circ Res. 2010;107:689-699.)
引用
收藏
页码:689 / 699
页数:11
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