Controlling metabolism and cell death: At the heart of mitochondrial calcium signalling

被引:89
作者
Murgia, Marta [1 ]
Giorg, Carlotta [2 ,3 ]
Pinton, Paolo [2 ,3 ]
Rizzuto, Rosario [1 ]
机构
[1] Univ Padua, Dept Biomed Sci, I-35121 Padua, Italy
[2] Univ Ferrara, Dept Expt & Diagnost Med, Sect Gen Pathol, Interdisciplinary Ctr Study Inflammat, I-44100 Ferrara, Italy
[3] Univ Ferrara, Emilia Romagna Lab BioPharmaNet, I-44100 Ferrara, Italy
关键词
Calcium; Mitochondria; Metabolism; Cell death; Apoptosis; ENDOPLASMIC-RETICULUM CA2+; APOPTOSIS-INDUCING FACTOR; TO-BEAT OSCILLATIONS; PROTEIN-KINASE-C; PERMEABILITY TRANSITION; INTRACELLULAR CA2+; PRESSURE-OVERLOAD; DOWN-REGULATION; CYCLOPHILIN-D; BCL-2;
D O I
10.1016/j.yjmcc.2009.03.003
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Transient increases in intracellular calcium concentration activate and coordinate a wide variety of cellular processes in virtually every cell type. This review describes the main homeostatic mechanisms that control Ca2+ transients, focusing on the mitochondrial checkpoint. We subsequently extend this paradigm to the cardiomyocyte and to the interplay between cytosol, endoplasmic reticulum and mitochondria that occurs beat-to-beat in excitation-contraction coupling. The mechanisms whereby mitochondria decode fast cytosolic calcium spikes are discussed in the light of the results obtained with recombinant photoproteins targeted to the mitochondrial matrix of contracting cardiomyocytes. Mitochondrial calcium homeostasis is then highlighted as a crucial point of convergence of the environmental signals that mediate cardiac cell death, both by necrosis and by apoptosis. Altogether we point to a role of the mitochondrion as an integrator of calcium signalling and a fundamental decision maker in cardiomyocyte metabolism and survival. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:781 / 788
页数:8
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