Faculty of Environmental and Life Sciences, University of Southampton, Southampton SO17 1BJ, UK.
Centre for Human Development, Stem Cells and Regeneration, School of Biological Sciences, University of Southampton, Southampton SO17 1BJ, UK.
Cells. 2022 Mar 9;11(6):937. doi: 10.3390/cells11060937.
Neuronal polarity established in developing neurons ensures proper function in the mature nervous system. As functionally distinct cellular compartments, axons and dendrites often require different subsets of proteins to maintain synaptic transmission and overall order. Although neurons in the mature CNS do not regenerate throughout life, their interactions with their extracellular environment are dynamic. The axon remains an overall protected area of the neuron where only certain proteins have access throughout the lifespan of the cell. This is in comparison to the somatodendritic compartment, where although it too has a specialised subset of proteins required for its maintenance, many proteins destined for the axonal compartment must first be trafficked through the former. Recent research has shown that axonal proteins contain specific axon-targeting motifs that permit access to the axonal compartment as well as downstream targeting to the axonal membrane. These motifs target proteins to the axonal compartment by a variety of mechanisms including: promoting segregation into axon-targeted secretory vesicles, increasing interaction with axonal kinesins and enhancing somatodendritic endocytosis. In this review, we will discuss axon-targeting motifs within the context of established neuron trafficking mechanisms. We will also include examples of how these motifs have been applied to target proteins to the axonal compartment to improve both tools for the study of axon biology, and for use as potential therapeutics for axonopathies.
在发育中的神经元中建立的神经元极性确保了成熟神经系统的正常功能。作为功能不同的细胞区室,轴突和树突通常需要不同的蛋白质亚基来维持突触传递和整体秩序。尽管成熟中枢神经系统中的神经元在整个生命周期内不会再生,但它们与细胞外环境的相互作用是动态的。轴突仍然是神经元的整体保护区,只有某些蛋白质在细胞的整个生命周期内都可以进入。相比之下,树突状突节区室虽然也有维持其功能所需的专门蛋白质亚基,但许多注定要进入轴突区室的蛋白质首先必须通过前者进行运输。最近的研究表明,轴突蛋白含有特定的轴突靶向基序,允许进入轴突区室以及下游靶向轴突膜。这些基序通过多种机制将蛋白质靶向轴突区室,包括:促进分离到轴突靶向分泌小泡中,增加与轴突驱动蛋白的相互作用,并增强树突状突内吞作用。在这篇综述中,我们将在已建立的神经元运输机制的背景下讨论轴突靶向基序。我们还将包括如何将这些基序应用于将蛋白质靶向轴突区室的示例,以提高轴突生物学研究的工具,并作为治疗轴突病的潜在治疗方法。