Kodavati Manohar, Wang Haibo, Hegde Muralidhar L
Department of Neurosurgery, Center for Neuroregeneration, Houston Methodist Research Institute, Houston, TX 77030, USA.
Department of Neurosurgery, Weill Medical College, New York, NY 10065, USA.
Cells. 2020 Apr 24;9(4):1065. doi: 10.3390/cells9041065.
Mitochondria plays privotal role in diverse pathways that regulate cellular function and survival, and have emerged as a prime focus in aging and age-associated motor neuron diseases (MNDs), such as amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Accumulating evidence suggests that many amyloidogenic proteins, including MND-associated RNA/DNA-binding proteins fused in sarcoma (FUS) and TAR DNA binding protein (TDP)-43, are strongly linked to mitochondrial dysfunction. Animal model and patient studies have highlighted changes in mitochondrial structure, plasticity, replication/copy number, mitochondrial DNA instability, and altered membrane potential in several subsets of MNDs, and these observations are consistent with the evidence of increased excitotoxicity, induction of reactive oxygen species, and activation of intrinsic apoptotic pathways. Studies in MND rodent models also indicate that mitochondrial abnormalities begin prior to the clinical and pathological onset of the disease, suggesting a causal role of mitochondrial dysfunction. Our recent studies, which demonstrated the involvement of specific defects in DNA break-ligation mediated by DNA ligase 3 (LIG3) in FUS-associated ALS, raised a key question of its potential implication in mitochondrial DNA transactions because LIG3 is essential for both mitochondrial DNA replication and repair. This question, as well as how wild-type and mutant MND-associated factors affect mitochondria, remain to be elucidated. These new investigation avenues into the mechanistic role of mitochondrial dysfunction in MNDs are critical to identify therapeutic targets to alleviate mitochondrial toxicity and its consequences. In this article, we critically review recent advances in our understanding of mitochondrial dysfunction in diverse subgroups of MNDs and discuss challenges and future directions.
线粒体在调节细胞功能和存活的多种途径中发挥着关键作用,并已成为衰老及与年龄相关的运动神经元疾病(MNDs)(如肌萎缩侧索硬化症(ALS)和额颞叶痴呆(FTD))的主要研究焦点。越来越多的证据表明,许多淀粉样蛋白,包括与MND相关的RNA/DNA结合蛋白肉瘤融合蛋白(FUS)和TAR DNA结合蛋白(TDP)-43,都与线粒体功能障碍密切相关。动物模型和患者研究突出了MNDs几个亚组中线粒体结构、可塑性、复制/拷贝数、线粒体DNA不稳定性以及膜电位改变等变化,这些观察结果与兴奋性毒性增加、活性氧生成以及内在凋亡途径激活的证据一致。对MND啮齿动物模型的研究还表明,线粒体异常在疾病的临床和病理发作之前就已出现,提示线粒体功能障碍具有因果作用。我们最近的研究表明,DNA连接酶3(LIG3)介导的DNA断裂连接中的特定缺陷参与了FUS相关的ALS,这引发了一个关键问题,即其在线粒体DNA事务中的潜在影响,因为LIG3对于线粒体DNA复制和修复都是必不可少的。这个问题以及野生型和突变型MND相关因子如何影响线粒体,仍有待阐明。这些关于线粒体功能障碍在MNDs中的机制作用的新研究途径对于确定减轻线粒体毒性及其后果的治疗靶点至关重要。在本文中,我们批判性地回顾了我们对MNDs不同亚组中线粒体功能障碍理解的最新进展,并讨论了挑战和未来方向。