Feil Family Brain and Mind Research Institute, Weill Cornell Medicine, New York, NY, 10065, USA.
Department of Neurology, Cantonal Hospital Aarau, 5001, Aarau, Switzerland.
Cell Mol Life Sci. 2021 Mar;78(5):2169-2183. doi: 10.1007/s00018-020-03625-5. Epub 2020 Sep 5.
Cerebral ischemia-reperfusion increases intraneuronal levels of ubiquitinated proteins, but the factors driving ubiquitination and whether it results from altered proteostasis remain unclear. To address these questions, we used in vivo and in vitro models of cerebral ischemia-reperfusion, in which hippocampal slices were transiently deprived of oxygen and glucose to simulate ischemia followed by reperfusion, or the middle cerebral artery was temporarily occluded in mice. We found that post-ischemic ubiquitination results from two key steps: restoration of ATP at reperfusion, which allows initiation of protein ubiquitination, and free radical production, which, in the presence of sufficient ATP, increases ubiquitination above pre-ischemic levels. Surprisingly, free radicals did not augment ubiquitination through inhibition of the proteasome as previously believed. Although reduced proteasomal activity was detected after ischemia, this was neither caused by free radicals nor sufficient in magnitude to induce appreciable accumulation of proteasomal target proteins or ubiquitin-proteasome reporters. Instead, we found that ischemia-derived free radicals inhibit deubiquitinases, a class of proteases that cleaves ubiquitin chains from proteins, which was sufficient to elevate ubiquitination after ischemia. Our data provide evidence that free radical-dependent deubiquitinase inactivation rather than proteasomal inhibition drives ubiquitination following ischemia-reperfusion, and as such call for a reevaluation of the mechanisms of post-ischemic ubiquitination, previously attributed to altered proteostasis. Since deubiquitinase inhibition is considered an endogenous neuroprotective mechanism to shield proteins from oxidative damage, modulation of deubiquitinase activity may be of therapeutic value to maintain protein integrity after an ischemic insult.
脑缺血再灌注会增加神经元内泛素化蛋白的水平,但驱动泛素化的因素以及它是否是由蛋白质稳态的改变引起的仍不清楚。为了解决这些问题,我们使用了脑缺血再灌注的体内和体外模型,其中海马切片短暂地缺氧和葡萄糖以模拟缺血,然后再灌注,或在小鼠中暂时阻塞大脑中动脉。我们发现,缺血后泛素化是由两个关键步骤引起的:再灌注时 ATP 的恢复,这允许启动蛋白质泛素化,以及自由基的产生,在有足够的 ATP 的情况下,泛素化水平会高于缺血前的水平。令人惊讶的是,自由基并没有像以前认为的那样通过抑制蛋白酶体来增加泛素化。尽管在缺血后检测到蛋白酶体活性降低,但这既不是自由基引起的,也没有达到足以诱导蛋白酶体靶蛋白或泛素-蛋白酶体报告蛋白明显积累的程度。相反,我们发现缺血衍生的自由基抑制去泛素化酶,一类从蛋白质上切割泛素链的蛋白酶,这足以在缺血后增加泛素化。我们的数据提供了证据,表明自由基依赖性去泛素化酶失活而不是蛋白酶体抑制驱动缺血再灌注后的泛素化,因此需要重新评估先前归因于蛋白质稳态改变的缺血后泛素化的机制。由于去泛素化酶抑制被认为是一种内源性的神经保护机制,可防止蛋白质免受氧化损伤,因此调节去泛素化酶的活性可能对维持缺血损伤后的蛋白质完整性具有治疗价值。