VDAC regulation of mitochondrial calcium flux: From channel biophysics to disease

被引:74
|
作者
Rosencrans, William M. [1 ]
Rajendran, Megha [1 ]
Bezrukov, Sergey M. [1 ]
Rostovtseva, Tatiana K. [1 ]
机构
[1] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Sect Mol Transport, NIH, 9000 Rockville Pike,Bldg 29B,Room 1G09, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
Voltage-dependent anion channel; Mitochondrial outer membrane; Mitochondrial associated membrane; -synuclein; Calcium signaling; Voltage gating; Ion selectivity; Protein-protein interaction; DEPENDENT ANION CHANNEL; CHOLESTEROL BINDING-SITES; ALPHA-SYNUCLEIN; MEMBRANE-PROTEIN; OUTER-MEMBRANE; ENDOPLASMIC-RETICULUM; MECHANISM; DYNAMICS; TRANSLOCATION; PERMEABILITY;
D O I
10.1016/j.ceca.2021.102356
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Voltage-dependent anion channel (VDAC), the most abundant mitochondrial outer membrane protein, is important for a variety of mitochondrial functions including metabolite exchange, calcium transport, and apoptosis. While VDAC?s role in shuttling metabolites between the cytosol and mitochondria is well established, there is a growing interest in understanding the mechanisms of its regulation of mitochondrial calcium transport. Here we review the current literature on VDAC?s role in calcium signaling, its biophysical properties, physiological function, and pathology focusing on its importance in cardiac diseases. We discuss the specific biophysical properties of the three VDAC isoforms in mammalian cells?VDAC 1, 2, and 3?in relationship to calcium transport and their distinct roles in cell physiology and disease. Highlighting the emerging evidence that cytosolic proteins interact with VDAC and regulate its calcium permeability, we advocate for continued investigation into the VDAC interactome at the contact sites between mitochondria and organelles and its role in mitochondrial calcium transport.
引用
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页数:10
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