Kiryu-Seo Sumiko, Kiyama Hiroshi
Department of Functional Anatomy and Neuroscience, Graduate School of Medicine, Nagoya University. 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Department of Functional Anatomy and Neuroscience, Graduate School of Medicine, Nagoya University. 65 Tsurumai-cho, Showa-ku, Nagoya 466-8550, Japan.
Neurosci Res. 2019 Feb;139:42-47. doi: 10.1016/j.neures.2018.08.014. Epub 2018 Sep 1.
Over the last decade, mitochondrial dynamics beyond function during axon regeneration/degeneration have received attention. Axons have an effective delivery system of mitochondria shuttling between soma and axonal terminals, due to their polarized structure. The proper axonal transport of mitochondria, coordinated with mitochondrial fission/fusion and clearance, is vital for supplying high power energy in injured axons. Many researchers have studied mitochondrial dynamics using in vitro cultured cells with significant progress reported. However, the in vitro culture system is missing a physiological environment including glial cells, immune cells, and endothelial cells, whose communications are indispensable to nerve regeneration/degeneration. In line with this, the understanding of mitochondrial behavior in injured axon in vivo is necessary for promoting the physiological understanding of damaged axons and the development of a therapeutic strategy. In this review, we focus on recent insights into in vivo mitochondrial dynamics during axonal regeneration/degeneration, and introduce the advances of mouse strains to visualize mitochondria in a neuron-specific or an injury-specific manner, which are extremely useful for nerve regeneration/degeneration studies.
在过去十年中,轴突再生/退化过程中线粒体功能之外的动力学受到了关注。由于轴突的极化结构,其具有一个有效的线粒体传递系统,可在胞体和轴突终末之间穿梭。线粒体的正常轴突运输,与线粒体的分裂/融合及清除相协调,对于为受损轴突提供高能量至关重要。许多研究人员使用体外培养细胞研究线粒体动力学,并报告了显著进展。然而,体外培养系统缺乏包括神经胶质细胞、免疫细胞和内皮细胞在内的生理环境,而这些细胞间的通讯对于神经再生/退化是不可或缺的。与此一致,了解体内受损轴突中的线粒体行为对于促进对受损轴突的生理理解以及治疗策略的开发是必要的。在这篇综述中,我们关注轴突再生/退化过程中体内线粒体动力学的最新见解,并介绍以神经元特异性或损伤特异性方式可视化线粒体的小鼠品系的进展,这对于神经再生/退化研究极为有用。