Vais Horia, Mallilankaraman Karthik, Mak Don-On Daniel, Hoff Henry, Payne Riley, Tanis Jessica E, Foskett J Kevin
Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Department of Physiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA; Department of Cell and Developmental Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Cell Rep. 2016 Jan 26;14(3):403-410. doi: 10.1016/j.celrep.2015.12.054. Epub 2016 Jan 7.
The mitochondrial uniporter (MCU) is an ion channel that mediates Ca(2+) uptake into the matrix to regulate metabolism, cell death, and cytoplasmic Ca(2+) signaling. Matrix Ca(2+) concentration is similar to that in cytoplasm, despite an enormous driving force for entry, but the mechanisms that prevent mitochondrial Ca(2+) overload are unclear. Here, we show that MCU channel activity is governed by matrix Ca(2+) concentration through EMRE. Deletion or charge neutralization of its matrix-localized acidic C terminus abolishes matrix Ca(2+) inhibition of MCU Ca(2+) currents, resulting in MCU channel activation, enhanced mitochondrial Ca(2+) uptake, and constitutively elevated matrix Ca(2+) concentration. EMRE-dependent regulation of MCU channel activity requires intermembrane space-localized MICU1, MICU2, and cytoplasmic Ca(2+). Thus, mitochondria are protected from Ca(2+) depletion and Ca(2+) overload by a unique molecular complex that involves Ca(2+) sensors on both sides of the inner mitochondrial membrane, coupled through EMRE.
线粒体单向转运体(MCU)是一种离子通道,介导钙离子摄取进入线粒体基质,以调节新陈代谢、细胞死亡和细胞质钙离子信号传导。尽管存在巨大的进入驱动力,但线粒体基质中的钙离子浓度与细胞质中的相似,而防止线粒体钙离子过载的机制尚不清楚。在这里,我们表明MCU通道活性通过EMRE受基质钙离子浓度的调控。其基质定位的酸性C末端的缺失或电荷中和消除了基质钙离子对MCU钙离子电流的抑制作用,导致MCU通道激活、线粒体钙离子摄取增强以及基质钙离子浓度持续升高。MCU通道活性的EMRE依赖性调控需要膜间隙定位的MICU1、MICU2和细胞质钙离子。因此,线粒体通过一种独特的分子复合物免受钙离子耗竭和过载的影响,该复合物涉及线粒体内膜两侧的钙离子传感器,并通过EMRE相互耦合。