Misgeld Thomas, Schwarz Thomas L
Technical University of Munich, Institute of Neuronal Cell Biology, Munich, Germany; German Center for Neurodegenerative Diseases, Munich, Germany; Munich Cluster for Systems Neurology, Munich, Germany; Center of Integrated Protein Science, Munich, Germany.
Department of Neurobiology, Harvard Medical School, Boston, MA, USA; F.M. Kirby Neurobiology Center, Children's Hospital, Boston, MA, USA.
Neuron. 2017 Nov 1;96(3):651-666. doi: 10.1016/j.neuron.2017.09.055.
Neurons have more extended and complex shapes than other cells and consequently face a greater challenge in distributing and maintaining mitochondria throughout their arbors. Neurons can last a lifetime, but proteins turn over rapidly. Mitochondria, therefore, need constant rejuvenation no matter how far they are from the soma. Axonal transport of mitochondria and mitochondrial fission and fusion contribute to this rejuvenation, but local protein synthesis is also likely. Maintenance of a healthy mitochondrial population also requires the clearance of damaged proteins and organelles. This involves degradation of individual proteins, sequestration in mitochondria-derived vesicles, organelle degradation by mitophagy and macroautophagy, and in some cases transfer to glial cells. Both long-range transport and local processing are thus at work in achieving neuronal mitostasis-the maintenance of an appropriately distributed pool of healthy mitochondria for the duration of a neuron's life. Accordingly, defects in the processes that support mitostasis are significant contributors to neurodegenerative disorders.
神经元的形状比其他细胞更为细长和复杂,因此在整个树突中分布和维持线粒体面临着更大的挑战。神经元可以存活一生,但蛋白质更新迅速。因此,无论线粒体距离胞体有多远,都需要不断更新。线粒体的轴突运输以及线粒体的分裂和融合有助于这种更新,但局部蛋白质合成也可能发挥作用。维持健康的线粒体群体还需要清除受损的蛋白质和细胞器。这涉及单个蛋白质的降解、线粒体衍生小泡中的隔离、通过线粒体自噬和巨自噬进行的细胞器降解,在某些情况下还涉及向神经胶质细胞的转移。因此,长距离运输和局部处理都在实现神经元线粒体稳态中发挥作用,即在神经元的生命周期内维持健康线粒体的适当分布库。相应地,支持线粒体稳态的过程中的缺陷是神经退行性疾病的重要促成因素。