Mitochondrial shape changes: orchestrating cell pathophysiology

被引:240
作者
Campello, Silvia [1 ]
Scorrano, Luca [1 ,2 ]
机构
[1] Univ Geneva, Dept Cell Physiol & Metab, CH-1206 Geneva, Switzerland
[2] Venetian Inst Mol Med, Dulbecco Telethon Inst, I-35129 Padua, Italy
关键词
mitochondria; fusion/fission; T cell; migration; adaptive/innate immunity; ENDOPLASMIC-RETICULUM; CYTOCHROME-C; CALCIUM SIGNALS; FISSION; PROTEIN; CRISTAE; FUSION; OPA1; APOPTOSIS; DYNAMICS;
D O I
10.1038/embor.2010.115
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mitochondria are highly dynamic organelles, the location, size and distribution of which are controlled by a family of proteins that modulate mitochondrial fusion and fission. Recent evidence indicates that mitochondrial morphology is crucial for cell physiology, as changes in mitochondrial shape have been linked to neuro-degeneration, calcium signalling, lifespan and cell death. Because immune cells contain few mitochondria, these organelles have been considered to have only a marginal role in this physiological context-which is conversely well characterized from the point of view of signalling. Nevertheless, accumulating evidence shows that mitochondrial dynamics have an impact on the migration and activation of immune cells and on the innate immune response. Here, we discuss the roles of mitochondrial dynamics in cell pathophysiology and consider how studying dynamics in the context of the immune system could increase our knowledge about the role of dynamics in key signalling cascades.
引用
收藏
页码:678 / 684
页数:7
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