Department of Neuroscience and Center for Molecular Neurobiology, The Ohio State University, Columbus, USA.
Prog Neurobiol. 2011 Jul;94(2):115-32. doi: 10.1016/j.pneurobio.2011.04.009. Epub 2011 Apr 22.
Precise localization of various ion channels into proper subcellular compartments is crucial for neuronal excitability and synaptic transmission. Axonal K(+) channels that are activated by depolarization of the membrane potential participate in the repolarizing phase of the action potential, and hence regulate action potential firing patterns, which encode output signals. Moreover, some of these channels can directly control neurotransmitter release at axonal terminals by constraining local membrane excitability and limiting Ca(2+) influx. K(+) channels differ not only in biophysical and pharmacological properties, but in expression and subcellular distribution as well. Importantly, proper targeting of channel proteins is a prerequisite for electrical and chemical functions of axons. In this review, we first highlight recent studies that demonstrate different roles of axonal K(+) channels in the local regulation of axonal excitability. Next, we focus on research progress in identifying axonal targeting motifs and machinery of several different types of K(+) channels present in axons. Regulation of K(+) channel targeting and activity may underlie a novel form of neuronal plasticity. This research field can contribute to generating novel therapeutic strategies through manipulating neuronal excitability in treating neurological diseases, such as multiple sclerosis, neuropathic pain, and Alzheimer's disease.
各种离子通道在适当的亚细胞隔室中的精确定位对于神经元兴奋性和突触传递至关重要。膜电位去极化激活的轴突 K(+)通道参与动作电位的复极化阶段,从而调节动作电位的发放模式,从而编码输出信号。此外,这些通道中的一些可以通过限制局部膜兴奋性和限制 Ca(2+)内流直接控制轴突末端的神经递质释放。K(+)通道不仅在生理和药理学特性上有所不同,而且在表达和亚细胞分布上也有所不同。重要的是,通道蛋白的正确靶向是轴突电和化学功能的前提。在这篇综述中,我们首先强调了最近的研究,这些研究表明轴突 K(+)通道在局部调节轴突兴奋性方面具有不同的作用。接下来,我们将重点介绍鉴定几种存在于轴突中的不同类型 K(+)通道的轴突靶向基序和机制的研究进展。K(+)通道靶向和活性的调节可能是一种新形式的神经元可塑性的基础。这个研究领域可以通过操纵神经元兴奋性来治疗神经疾病,如多发性硬化症、神经性疼痛和阿尔茨海默病,为开发新的治疗策略做出贡献。