Mitochondrial calcium uniporter regulator 1 (MCUR1) regulates the calcium threshold for the mitochondrial permeability transition
Author(s) -
Dipayan Chaudhuri,
Daniel J. Artiga,
Sunday A. Abiria,
David E. Clapham
Publication year - 2016
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.1602264113
Subject(s) - mitochondrial permeability transition pore , microbiology and biotechnology , mitochondrion , uniporter , biology , mitochondrial apoptosis induced channel , regulator , calcium , calcium signaling , inner mitochondrial membrane , mitochondrial membrane transport protein , membrane potential , programmed cell death , permeability (electromagnetism) , chemistry , biophysics , biochemistry , signal transduction , apoptosis , cytosol , gene , membrane , enzyme , organic chemistry
During the mitochondrial permeability transition, a large channel in the inner mitochondrial membrane opens, leading to the loss of multiple mitochondrial solutes and cell death. Key triggers include excessive reactive oxygen species and mitochondrial calcium overload, factors implicated in neuronal and cardiac pathophysiology. Examining the differential behavior of mitochondrial Ca(2+) overload in Drosophila versus human cells allowed us to identify a gene, MCUR1, which, when expressed in Drosophila cells, conferred permeability transition sensitive to electrophoretic Ca(2+) uptake. Conversely, inhibiting MCUR1 in mammalian cells increased the Ca(2+) threshold for inducing permeability transition. The effect was specific to the permeability transition induced by Ca(2+), and such resistance to overload translated into improved cell survival. Thus, MCUR1 expression regulates the Ca(2+) threshold required for permeability transition.
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