1 Department of Biological Sciences, University of South Carolina, Columbia, SC, USA.
2 Department of Neurobiology and Anatomy, Drexel University College of Medicine, Philadelphia, PA, USA.
Neuroscientist. 2018 Apr;24(2):111-129. doi: 10.1177/1073858417712668. Epub 2017 Jun 8.
Intra-axonal protein synthesis has been shown to play critical roles in both development and repair of axons. Axons provide long-range connectivity in the nervous system, and disruption of their function and/or structure is seen in several neurological diseases and disorders. Axonally synthesized proteins or losses in axonally synthesized proteins contribute to neurodegenerative diseases, neuropathic pain, viral transport, and survival of axons. Increasing sensitivity of RNA detection and quantitation coupled with methods to isolate axons to purity has shown that a surprisingly complex transcriptome exists in axons. This extends across different species, neuronal populations, and physiological conditions. These studies have helped define the repertoire of neuronal mRNAs that can localize into axons and imply previously unrecognized functions for local translation in neurons. Here, we review the current state of transcriptomics studies of isolated axons, contrast axonal mRNA profiles between different neuronal types and growth states, and discuss how mRNA transport into and translation within axons contribute to neurological disorders.
轴内蛋白质合成已被证明在轴突的发育和修复中起着关键作用。轴突在神经系统中提供长距离的连接,其功能和/或结构的破坏可见于几种神经疾病和障碍中。轴突合成的蛋白质或轴突合成的蛋白质的损失导致神经退行性疾病、神经性疼痛、病毒运输和轴突的存活。RNA 检测和定量的敏感性增加以及分离轴突至纯度的方法表明,轴突中存在令人惊讶的复杂转录组。这跨越了不同的物种、神经元群体和生理条件。这些研究有助于确定可以定位到轴突中的神经元 mRNA 谱,并暗示局部翻译在神经元中的以前未被认识到的功能。在这里,我们回顾了分离轴突的转录组学研究的现状,比较了不同神经元类型和生长状态之间的轴突 mRNA 谱,并讨论了 mRNA 向轴突内的运输和翻译如何导致神经障碍。