Department of Cellular and Molecular Medicine, University of Ottawa Heart Institute, University of Ottawa, Ontario K1H 8M5, Canada.
J Biol Chem. 2011 Feb 11;286(6):4772-82. doi: 10.1074/jbc.M110.167155. Epub 2010 Nov 1.
Mitochondrial dynamics have been extensively studied in the context of classical cell death models involving Bax-mediated cytochrome c release. Excitotoxic neuronal loss is a non-classical death signaling pathway that occurs following overactivation of glutamate receptors independent of Bax activation. Presently, the role of mitochondrial dynamics in the regulation of excitotoxicity remains largely unknown. Here, we report that NMDA-induced excitotoxicity results in defects in mitochondrial morphology as evident by the presence of excessive fragmented mitochondria, cessation of mitochondrial fusion, and cristae dilation. Up-regulation of the mitochondrial inner membrane GTPase, Opa1, is able to restore mitochondrial morphology and protect neurons against excitotoxic injury. Opa1 functions downstream of the calcium-dependent protease, calpain. Inhibition of calpain activity by calpastatin, an endogenous calpain inhibitor, significantly rescued mitochondrial defects and maintained neuronal survival. Opa1 was required for calpastatin-mediated neuroprotection because the enhanced survival found following NMDA-induced toxicity was significantly reduced upon loss of Opa1. Our results define a mechanism whereby breakdown of the mitochondrial network mediated through loss of Opa1 function contributes to neuronal death following excitotoxic neuronal injury. These studies suggest Opa1 as a potential therapeutic target to promote neuronal survival following acute brain damage and neurodegenerative diseases.
线粒体动力学在涉及 Bax 介导的细胞色素 c 释放的经典细胞死亡模型的背景下得到了广泛研究。兴奋性神经元丢失是一种非经典的死亡信号通路,它发生在谷氨酸受体过度激活而不依赖于 Bax 激活的情况下。目前,线粒体动力学在调节兴奋性毒性中的作用在很大程度上仍然未知。在这里,我们报告 NMDA 诱导的兴奋性毒性导致线粒体形态缺陷,表现为过多的碎片化线粒体、线粒体融合停止和嵴扩张。线粒体内膜 GTP 酶 Opa1 的上调能够恢复线粒体形态并保护神经元免受兴奋性毒性损伤。Opa1 是钙依赖性蛋白酶 calpain 的下游分子。内源性 calpain 抑制剂 calpastatin 通过抑制 calpain 活性,显著挽救了线粒体缺陷并维持神经元存活。Opa1 是 calpastatin 介导的神经保护所必需的,因为 NMDA 诱导的毒性后发现的增强的存活在 Opa1 缺失时显著降低。我们的结果定义了一种机制,即通过 Opa1 功能丧失介导的线粒体网络的破坏导致兴奋性神经元损伤后神经元死亡。这些研究表明 Opa1 是促进急性脑损伤和神经退行性疾病后神经元存活的潜在治疗靶点。