1. Academic Validation
  2. VDAC2-specific cellular functions and the underlying structure

VDAC2-specific cellular functions and the underlying structure

  • Biochim Biophys Acta. 2016 Oct;1863(10):2503-14. doi: 10.1016/j.bbamcr.2016.04.020.
Shamim Naghdi 1 György Hajnóczky 2
Affiliations

Affiliations

  • 1 MitoCare Center for Mitochondrial Imaging Research and Diagnostics, Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA, USA. Electronic address: [email protected].
  • 2 MitoCare Center for Mitochondrial Imaging Research and Diagnostics, Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, Philadelphia, PA, USA. Electronic address: [email protected].
Abstract

Voltage Dependent Anion-selective Channel 2 (VDAC2) contributes to oxidative metabolism by sharing a role in solute transport across the outer mitochondrial membrane (OMM) with Other isoforms of the VDAC family, VDAC1 and VDAC3. Recent studies revealed that VDAC2 also has a distinctive role in mediating sarcoplasmic reticulum to mitochondria local CA(2+) transport at least in cardiomyocytes, which is unlikely to be explained simply by the expression level of VDAC2. Furthermore, a strictly isoform-dependent VDAC2 function was revealed in the mitochondrial import and OMM-permeabilizing function of pro-apoptotic Bcl-2 Family proteins, primarily Bak in many cell types. In addition, emerging evidence indicates a variety of Other isoform-specific engagements for VDAC2. Since VDAC isoforms display 75% sequence similarity, the distinctive structure underlying VDAC2-specific functions is an intriguing problem. In this paper we summarize studies of VDAC2 structure and functions, which suggest a fundamental and exclusive role for VDAC2 in health and disease. This article is part of a Special Issue entitled: Mitochondrial Channels edited by Pierre Sonveaux, Pierre Maechler and Jean-Claude Martinou.

Keywords

Apoptosis; Bak; Bax; Bid; Calcium; Mitochondria; Sarcoplasmic reticulum; VDAC2.

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