4.7 Article

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

Journal

CIRCULATION RESEARCH
Volume 107, Issue 6, Pages 689-699

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/CIRCRESAHA.110.225714

Keywords

mitochondrial fusion; endoplasmic reticulum; calcium; apoptosis; mitochondrial permeability transition

Funding

  1. National Heart, Lung, and Blood Institute, NIH
  2. Swiss National Science Foundation
  3. Telethon Italy
  4. Oncosuisse

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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.)

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