Maddison Daniel C, Mattedi Francesca, Vagnoni Alessio, Smith Gaynor Ann
UK Dementia Research Institute, School of Medicine, Cardiff University, Cardiff CF24 4HQ, United Kingdom.
Department of Basic and Clinical Neurosciences, Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London SE5 9RX, United Kingdom.
Cold Spring Harb Protoc. 2023 Feb 1;2023(2):75-83. doi: 10.1101/pdb.top107819.
Neuronal survival depends on the generation of ATP from an ever-changing mitochondrial network. This requires a fine balance between the constant degradation of damaged mitochondria, biogenesis of new mitochondria, movement along microtubules, dynamic processes, and adequate functional capacity to meet firing demands. The distribution of mitochondria needs to be tightly controlled throughout the entire neuron, including its projections. Axons in particular can be enormous structures compared to the size of the cell soma, and how mitochondria are maintained in these compartments is poorly defined. Mitochondrial dysfunction in neurons is associated with aging and neurodegenerative diseases, with the axon being preferentially vulnerable to destruction. offer a unique way to study these organelles in fully differentiated adult neurons in vivo. Here, we briefly review the regulation of neuronal mitochondria in health, aging, and disease and introduce two methodological approaches to study mitochondrial dynamics and transport in axons using the wing system.
神经元的存活依赖于不断变化的线粒体网络产生ATP。这需要在受损线粒体的持续降解、新线粒体的生物合成、沿微管的移动、动态过程以及满足放电需求的足够功能能力之间保持精细平衡。线粒体的分布需要在整个神经元(包括其突起)中受到严格控制。与细胞体的大小相比,轴突尤其可能是巨大的结构,而线粒体如何在这些区域中维持尚不清楚。神经元中的线粒体功能障碍与衰老和神经退行性疾病有关,轴突尤其容易受到破坏。 提供了一种在体内完全分化的成年神经元中研究这些细胞器的独特方法。在这里,我们简要回顾健康、衰老和疾病状态下神经元线粒体的调节,并介绍两种使用翼系统研究轴突中线粒体动力学和运输的方法。