Chaudhuri Dipayan, Artiga Daniel J, Abiria Sunday A, Clapham David E
Howard Hughes Medical Institute, Department of Cardiology, Boston Children's Hospital, Boston, MA 02115;
Harvard University, Cambridge, MA 02138;
Proc Natl Acad Sci U S A. 2016 Mar 29;113(13):E1872-80. doi: 10.1073/pnas.1602264113. Epub 2016 Mar 14.
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.
在线粒体通透性转换过程中,线粒体内膜上的一个大通道打开,导致多种线粒体溶质流失并引发细胞死亡。关键触发因素包括过量的活性氧和线粒体钙超载,这些因素与神经元和心脏病理生理学有关。研究果蝇细胞与人类细胞中线粒体Ca(2+)超载的差异行为,使我们鉴定出一个基因MCUR1,当它在果蝇细胞中表达时,赋予对电泳性Ca(2+)摄取敏感的通透性转换。相反,在哺乳动物细胞中抑制MCUR1会提高诱导通透性转换的Ca(2+)阈值。这种效应对于由Ca(2+)诱导的通透性转换具有特异性,并且这种对超载的抗性转化为细胞存活率的提高。因此,MCUR1的表达调节通透性转换所需的Ca(2+)阈值。