VDAC regulation of mitochondrial calcium flux: From channel biophysics to disease.
Autor: | Rosencrans WM; Section on Molecular Transport, Eunice Kennedy Shriver. National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, 20892, United States., Rajendran M; Section on Molecular Transport, Eunice Kennedy Shriver. National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, 20892, United States., Bezrukov SM; Section on Molecular Transport, Eunice Kennedy Shriver. National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, 20892, United States., Rostovtseva TK; Section on Molecular Transport, Eunice Kennedy Shriver. National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, 20892, United States. Electronic address: rostovtt@mail.nih.gov. |
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Jazyk: | angličtina |
Zdroj: | Cell calcium [Cell Calcium] 2021 Mar; Vol. 94, pp. 102356. Date of Electronic Publication: 2021 Jan 23. |
DOI: | 10.1016/j.ceca.2021.102356 |
Abstrakt: | 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. (Copyright © 2021 Elsevier Ltd. All rights reserved.) |
Databáze: | MEDLINE |
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