Loucks F Alexandra, Schroeder Emily K, Zommer Amelia E, Hilger Shea, Kelsey Natalie A, Bouchard Ron J, Blackstone Craig, Brewster Jay L, Linseman Daniel A
Research Service, Veterans Affairs Medical Center, Denver, Colorado, USA.
Brain Res. 2009 Jan 23;1250:63-74. doi: 10.1016/j.brainres.2008.10.081. Epub 2008 Nov 18.
The critical processes of mitochondrial fission and fusion are regulated by members of the dynamin family of GTPases. Imbalances in mitochondrial fission and fusion contribute to neuronal cell death. For example, increased fission mediated by the dynamin-related GTPase, Drp1, or decreased fusion resulting from inactivating mutations in the OPA1 GTPase, causes neuronal apoptosis and/or neurodegeneration. Recent studies indicate that post-translational processing regulates OPA1 function in non-neuronal cells and moreover, aberrant processing of OPA1 is induced during apoptosis. To date, the post-translational processing of OPA1 during neuronal apoptosis has not been examined. Here, we show that cerebellar granule neurons (CGNs) or neuroblastoma cells exposed to pro-apoptotic stressors display a novel N-terminal cleavage of OPA1 which is blocked by either pan-caspase or caspase-8 selective inhibitors. OPA1 cleavage occurs concurrently with mitochondrial fragmentation and cytochrome c release in CGNs deprived of depolarizing potassium (5K condition). Although a caspase-8 selective inhibitor prevents both 5K-induced OPA1 cleavage and mitochondrial fragmentation, recombinant caspase-8 fails to cleave OPA1 in vitro. In marked contrast, either caspase-8 or caspase-3 stimulates OPA1 cleavage in digitonin-permeabilized rat brain mitochondria, suggesting that OPA1 is cleaved by an intermembrane space protease which is regulated by active caspases. Finally, the N-terminal truncation of OPA1 induced during neuronal apoptosis removes an essential residue (K301) within the GTPase domain. These data are the first to demonstrate OPA1 cleavage during neuronal apoptosis and they implicate caspases as indirect regulators of OPA1 processing in degenerating neurons.
线粒体分裂和融合的关键过程由GTP酶的发动蛋白家族成员调控。线粒体分裂和融合的失衡会导致神经元细胞死亡。例如,由发动蛋白相关GTP酶Drp1介导的分裂增加,或OPA1 GTP酶失活突变导致的融合减少,都会引起神经元凋亡和/或神经退行性变。最近的研究表明,翻译后加工在非神经元细胞中调节OPA1功能,此外,在细胞凋亡过程中会诱导OPA1的异常加工。迄今为止,尚未研究神经元凋亡过程中OPA1的翻译后加工。在此,我们表明,暴露于促凋亡应激源的小脑颗粒神经元(CGN)或神经母细胞瘤细胞显示出OPA1的一种新的N端切割,这种切割被泛半胱天冬酶或半胱天冬酶-8选择性抑制剂阻断。在缺乏去极化钾的CGN(5K条件)中,OPA1切割与线粒体碎片化和细胞色素c释放同时发生。虽然半胱天冬酶-8选择性抑制剂可防止5K诱导的OPA1切割和线粒体碎片化,但重组半胱天冬酶-8在体外不能切割OPA1。与之形成鲜明对比的是,半胱天冬酶-8或半胱天冬酶-3可刺激洋地黄皂苷通透的大鼠脑线粒体中的OPA1切割,这表明OPA1是由一种受活性半胱天冬酶调节的膜间隙蛋白酶切割的。最后,神经元凋亡过程中诱导的OPA1 N端截短去除了GTP酶结构域内的一个必需残基(K301)。这些数据首次证明了神经元凋亡过程中OPA1的切割,并表明半胱天冬酶是退化神经元中OPA1加工的间接调节因子。