Pharmacological modulation of mitochondrial calcium homeostasis

被引:40
作者
Arduino, Daniela M. [1 ,2 ,3 ]
Perocchi, Fabiana [1 ,2 ,3 ]
机构
[1] Ludwig Maximilians Univ Munchen, Gene Ctr, Dept Biochem, D-81377 Munich, Germany
[2] Helmholtz Zentrum Munchen, HDC, Inst Diabet & Obes, D-85764 Neuherberg, Germany
[3] German Natl Diabet Ctr DZD, D-85764 Neuherberg, Germany
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2018年 / 596卷 / 14期
关键词
mitochondria; calcium; drug screening; calcium signaling; mitochondrial calcium uniporter; drug discovery; RAT-LIVER MITOCHONDRIA; WOLF-HIRSCHHORN-SYNDROME; LOCAL-ANESTHETIC DRUGS; CA2+ UPTAKE; RUTHENIUM RED; ESSENTIAL COMPONENT; HEART-MITOCHONDRIA; ION TRANSPORT; CELL-DEATH; IN-VIVO;
D O I
10.1113/JP274959
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Mitochondria are pivotal organelles in calcium (Ca2+) handling and signalling, constituting intracellular checkpoints for numerous processes that are vital for cell life. Alterations in mitochondrial Ca2+ homeostasis have been linked to a variety of pathological conditions and are critical in the aetiology of several human diseases. Efforts have been taken to harness mitochondrial Ca2+ transport mechanisms for therapeutic intervention, but pharmacological compounds that direct and selectively modulate mitochondrial Ca2+ homeostasis are currently lacking. New avenues have, however, emerged with the breakthrough discoveries on the genetic identification of the main players involved in mitochondrial Ca2+ influx and efflux pathways and with recent hints towards a deep understanding of the function of these molecular systems. Here, we review the current advances in the understanding of the mechanisms and regulation of mitochondrial Ca2+ homeostasis and its contribution to physiology and human disease. We also introduce and comment on the recent progress towards a systems-level pharmacological targeting of mitochondrial Ca2+ homeostasis.
引用
收藏
页码:2717 / 2733
页数:17
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