INSERM UMR 641, Marseille F-13916, France.
Neurosci Lett. 2010 Dec 10;486(2):92-100. doi: 10.1016/j.neulet.2010.08.079. Epub 2010 Sep 21.
In neurons, voltage-gated sodium (Nav) channels underlie the generation and propagation of the action potential. The proper targeting and concentration of Nav channels at the axon initial segment (AIS) and at the nodes of Ranvier are therefore vital for neuronal function. In AIS and nodes, Nav channels are part of specific supra-molecular complexes that include accessory proteins, adhesion proteins and cytoskeletal adaptors. Multiple approaches, from biochemical characterization of protein-protein interactions to functional studies using mutant mice, have addressed the mechanisms of Nav channel targeting to AIS and nodes. This review summarizes our current knowledge of both the intrinsic determinants and the role of partner proteins in Nav targeting. A few fundamental trafficking mechanisms, such as selective endocytosis and diffusion/retention, have been characterized. However, a lot of exciting questions are still open, such as the mechanism of differentiated Nav subtype localization and targeting, and the possible interplay between electrogenesis properties and Nav concentration at the AIS and the nodes.
在神经元中,电压门控钠离子(Nav)通道是动作电位产生和传播的基础。因此,Nav 通道在轴突起始段(AIS)和郎飞结处的正确靶向和浓度对于神经元功能至关重要。在 AIS 和节点中,Nav 通道是特定超分子复合物的一部分,该复合物包括辅助蛋白、黏附蛋白和细胞骨架衔接蛋白。从蛋白质-蛋白质相互作用的生化特征分析到使用突变小鼠的功能研究,多种方法都已被用于研究 Nav 通道靶向 AIS 和节点的机制。这篇综述总结了我们目前对 Nav 靶向的内在决定因素和伴侣蛋白作用的了解。已经描述了一些基本的运输机制,如选择性内吞作用和扩散/保留。然而,仍有许多令人兴奋的问题尚未解决,例如不同 Nav 亚型定位和靶向的机制,以及 AIS 和节点处的电生成特性和 Nav 浓度之间可能存在的相互作用。