Src regulates membrane trafficking of the Kv3.1b channel

FEBS Lett. 2014 Jan 3;588(1):86-91. doi: 10.1016/j.febslet.2013.11.010. Epub 2013 Nov 26.

Abstract

The Kv3.1 channel plays a crucial role in regulating the high-frequency firing properties of neurons. Here, we determined whether Src regulates the subcellular distributions of the Kv3.1b channel. Co-expression of active Src induced a dramatic redistribution of Kv3.1b to the endoplasmic reticulum. Furthermore, co-expression of the Kv3.1b channel with active Src induced a remarkable decrease in the pool of Kv3.1b at the cell surface. Moreover, the co-expression of active Src results in a significant decrease in the peak current densities of the Kv3.1b channel, and a substantial alteration in the voltage dependence of its steady-state inactivation. Taken together, these results indicate that Src kinase may play an important role in regulating membrane trafficking of Kv3.1b channels.

Keywords: Kv3.1b; Membrane trafficking; Potassium channel; Src.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • COS Cells
  • Cell Membrane / metabolism*
  • Cell Membrane / physiology
  • Chlorocebus aethiops
  • Endoplasmic Reticulum / metabolism*
  • HEK293 Cells
  • Humans
  • Membrane Potentials / physiology
  • Mice
  • Mutagenesis, Site-Directed
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Nerve Tissue Proteins / physiology
  • Patch-Clamp Techniques
  • Protein Transport
  • Proto-Oncogene Proteins pp60(c-src) / genetics
  • Proto-Oncogene Proteins pp60(c-src) / metabolism*
  • Rats
  • Shaw Potassium Channels / genetics
  • Shaw Potassium Channels / metabolism*
  • Shaw Potassium Channels / physiology

Substances

  • Kcnc1 protein, rat
  • Nerve Tissue Proteins
  • Shaw Potassium Channels
  • Proto-Oncogene Proteins pp60(c-src)