ﻻ يوجد ملخص باللغة العربية
Voltage-gated sodium (Na$_mathrm{v}$) channels are responsible for the depolarizing phase of the action potential in most nerve cells, and Na$_mathrm{v}$ channel localization to the axon initial segment is vital to action potential initiation. Na$_mathrm{v}$ 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 Na$_mathrm{v}$ channel localization and dynamics within this neuronal compartment. This study uses single-particle tracking and photoactivation localization microscopy to analyze cell-surface Na$_mathrm{v}$1.6 within the soma of cultured hippocampal neurons. Mean-square displacement analysis of individual trajectories indicated that half of the somatic Na$_mathrm{v}$1.6 channels localized to stable nanoclusters $sim$230 nm in diameter. Strikingly, these domains were stabilized at specific sites on the cell membrane for >30 min, notably via an ankyrin-independent mechanism, indicating that the means by which Na$_mathrm{v}$1.6 nanoclusters are maintained in the soma is biologically different from axonal localization. Nonclustered Na$_mathrm{v}$1.6 channels showed anomalous diffusion, as determined by mean-square-displacement analysis. High-density single-particle tracking of Na$_mathrm{v}$ channels labeled with photoactivatable fluorophores in combination with Bayesian inference analysis was employed to characterize the surface nanoclusters. A subpopulation of mobile Na$_mathrm{v}$1.6 was observed to be transiently trapped in the nanoclusters. Somatic Na$_mathrm{v}$1.6 nanoclusters represent a new, to our knowledge, type of Na$_mathrm{v}$ channel localization, and are hypothesized to be sites of localized channel regulation.
Protein and lipid nanodomains are prevalent on the surface of mammalian cells. In particular, it has been recently recognized that ion channels assemble into surface nanoclusters in the soma of cultured neurons. However, the interactions of these mol
The syndecans represent an ongoing research field focused on their regulatory roles in normal and pathological conditions. Syndecans role in cancer progression becomes well-documented, implicating their importance in diagnosis and even proposing vari
Single molecule localization microscopy (SMLM) techniques enable imaging biological samples well beyond the diffraction limit of light, but they vary significantly in their spatial and temporal resolutions. High-order statistical analysis of temporal
Single molecule tracking in live cells is the ultimate tool to study subcellular protein dynamics, but it is often limited by the probe size and photostability. Due to these issues, long-term tracking of proteins in confined and crowded environments,
Super-resolution microscopy has catalyzed valuable insights into the sub-cellular, mechanistic details of many different biological processes across a wide range of cell types. Fluorescence polarization spectroscopy tools have also enabled important