Akin Elizabeth J, Solé Laura, Johnson Ben, Beheiry Mohamed El, Masson Jean-Baptiste, Krapf Diego, Tamkun Michael M
Cell and Molecular Biology Graduate Program, Colorado State University, Fort Collins, Colorado; Molecular, Cellular and Integrative Neuroscience Program, Colorado State University, Fort Collins, Colorado; Department of Biomedical Sciences, Colorado State University, Fort Collins, Colorado.
Department of Biomedical Sciences, Colorado State University, Fort Collins, Colorado.
Biophys J. 2016 Sep 20;111(6):1235-1247. doi: 10.1016/j.bpj.2016.08.016.
Voltage-gated sodium (Nav) channels are responsible for the depolarizing phase of the action potential in most nerve cells, and Nav channel localization to the axon initial segment is vital to action potential initiation. Nav channels in the soma play a role in the transfer of axonal output information to the rest of the neuron and in synaptic plasticity, although little is known about Nav channel localization and dynamics within this neuronal compartment. This study uses single-particle tracking and photoactivation localization microscopy to analyze cell-surface Nav1.6 within the soma of cultured hippocampal neurons. Mean-square displacement analysis of individual trajectories indicated that half of the somatic Nav1.6 channels localized to stable nanoclusters ∼230 nm in diameter. Strikingly, these domains were stabilized at specific sites on the cell membrane for >30 min, notably via an ankyrin-independent mechanism, indicating that the means by which Nav1.6 nanoclusters are maintained in the soma is biologically different from axonal localization. Nonclustered Nav1.6 channels showed anomalous diffusion, as determined by mean-square-displacement analysis. High-density single-particle tracking of Nav channels labeled with photoactivatable fluorophores in combination with Bayesian inference analysis was employed to characterize the surface nanoclusters. A subpopulation of mobile Nav1.6 was observed to be transiently trapped in the nanoclusters. Somatic Nav1.6 nanoclusters represent a new, to our knowledge, type of Nav channel localization, and are hypothesized to be sites of localized channel regulation.
电压门控钠(Nav)通道负责大多数神经细胞动作电位的去极化阶段,并且Nav通道定位于轴突起始段对于动作电位的起始至关重要。尽管对Nav通道在这个神经元区室内的定位和动态了解甚少,但胞体中的Nav通道在将轴突输出信息传递到神经元的其他部分以及在突触可塑性方面发挥作用。本研究使用单粒子追踪和光激活定位显微镜来分析培养的海马神经元胞体内的细胞表面Nav1.6。对单个轨迹的均方位移分析表明,胞体中一半的Nav1.6通道定位于直径约230 nm的稳定纳米簇。令人惊讶的是,这些结构域在细胞膜上的特定位置稳定存在超过30分钟,特别是通过一种不依赖锚蛋白的机制,这表明Nav1.6纳米簇在胞体中维持的方式在生物学上与轴突定位不同。通过均方位移分析确定,非簇状的Nav1.6通道表现出异常扩散。使用光激活荧光团标记的Nav通道的高密度单粒子追踪结合贝叶斯推理分析来表征表面纳米簇。观察到一部分可移动的Nav1.6短暂地被困在纳米簇中。据我们所知,胞体中的Nav1.6纳米簇代表一种新型的Nav通道定位,并且被推测为局部通道调节的位点。