Genetic Demonstration That the Plasma Membrane Maxianion Channel and Voltage-dependent Anion Channels Are Unrelated Proteins

Ravshan Z. Sabirov, Tatiana Sheiko, Hongtao Liu, Defeng Deng, Yasunobu Okada, William J. Craigen
2005 Journal of Biological Chemistry  
The maxianion channel is widely expressed in many cell types, where it fulfills a general physiological function as an ATP-conductive gate for cell-to-cell purinergic signaling. Establishing the molecular identity of this channel is crucial to understanding the mechanisms of regulated ATP release. A mitochondrial porin (voltage-dependent anion channel (VDAC)) located in the plasma membrane has long been considered as the molecule underlying the maxianion channel activity, based upon
more » ... ed upon similarities in the biophysical properties of these two channels and the purported presence of VDAC protein in the plasma membrane. We have deleted each of the three genes encoding the VDAC isoforms individually and collectively and demonstrate that maxianion channel (ϳ400 picosiemens) activity in VDAC-deficient mouse fibroblasts is unaltered. The channel activity is similar in VDAC1/VDAC3-double-deficient cells and in double-deficient cells with the VDAC2 protein depleted by RNA interference. VDAC deletion slightly down-regulated, but never abolished, the swelling-induced ATP release. The lack of correlation between VDAC protein expression and maxianion channel activity strongly argues against the long held hypothesis of plasmalemmal VDAC being the maxianion channel. . 2 The abbreviations used are: VDAC, voltage-dependent anion channel; pl-VDAC, plas-malemmal VDAC; MEF, mouse embryonic fibroblast(s); MAF, mouse adult fibroblast(s); dKO, double knockout; WT, wild type; RNAi, RNA interference; pS, picosiemens.
doi:10.1074/jbc.m509482200 pmid:16291750 fatcat:mxw556qvgfftrbkmgiaoct4yqu