Research Unit for Molecular Medicine, Aarhus University Hospital and Faculty of Health Sciences, Aarhus University , Aarhus , Denmark.
Free Radic Res. 2014 Feb;48(2):168-79. doi: 10.3109/10715762.2013.858147. Epub 2013 Nov 11.
Even though the deleterious effects of increased reactive oxygen species (ROS) levels have been implicated in a variety of neurodegenerative disorders, the triggering events that lead to the increased ROS and successive damages are still ill-defined. Mitochondria are the key organelles controlling the ROS balance, being their main source and also counteracting them by the action of the ROS scavenging system. Mitochondria, moreover, control the presence of ROS-damaged proteins by action of the protein quality control (PQC) system. One of its components is the mitochondrial chaperone Hsp60 assisting the folding of a subset of mitochondrial matrix proteins. Mutations in Hsp60 cause a late onset form of the neurodegenerative disease hereditary spastic paraplegia (SPG13). In this study, we aimed to address the molecular consequences of Hsp60 shortage. We here demonstrate that a heterozygous knockout Hsp60 model that recapitulates features of the human disease and exhibits increased oxidative stress in neuronal tissues. Moreover, we indicate that the increase of ROS is, at least in part, due to impaired folding of the manganese superoxide dismutase (MnSOD), a key antioxidant enzyme. We observed that the Hsp60 and MnSOD proteins interact. Based on these results, we propose that MnSOD is a substrate of the Hsp60 folding machinery and that under conditions of diminished availability of Hsp60, MnSOD is impaired in reaching the native state. This suggests a possible link between Hsp60-dependent PQC and the ROS scavenging systems that may have the function to increase ROS production under conditions of folding stress.
尽管活性氧(ROS)水平升高的有害影响与多种神经退行性疾病有关,但导致 ROS 升高和随后损伤的触发事件仍未明确定义。线粒体是控制 ROS 平衡的关键细胞器,是 ROS 的主要来源,也是通过 ROS 清除系统的作用来对抗 ROS。此外,线粒体通过蛋白质质量控制(PQC)系统来控制 ROS 损伤蛋白的存在。其组成部分之一是线粒体伴侣蛋白 Hsp60,它有助于一组线粒体基质蛋白的折叠。Hsp60 的突变导致神经退行性疾病遗传性痉挛性截瘫(SPG13)的迟发性发病形式。在这项研究中,我们旨在研究 Hsp60 缺乏的分子后果。我们在这里证明,一种杂合敲除 Hsp60 的模型可以重现人类疾病的特征,并在神经元组织中表现出氧化应激增加。此外,我们表明 ROS 的增加至少部分是由于锰超氧化物歧化酶(MnSOD)的折叠受损,MnSOD 是一种关键的抗氧化酶。我们观察到 Hsp60 和 MnSOD 蛋白相互作用。基于这些结果,我们提出 MnSOD 是 Hsp60 折叠机制的底物,并且在 Hsp60 可用性降低的情况下,MnSOD 受损,无法达到天然状态。这表明 Hsp60 依赖性 PQC 与 ROS 清除系统之间可能存在联系,该系统的功能可能是在折叠应激条件下增加 ROS 产生。