Shisa6 traps AMPA receptors at postsynaptic sites and prevents their desensitization during synaptic activity

Nat Commun. 2016 Mar 2:7:10682. doi: 10.1038/ncomms10682.

Abstract

Trafficking and biophysical properties of AMPA receptors (AMPARs) in the brain depend on interactions with associated proteins. We identify Shisa6, a single transmembrane protein, as a stable and directly interacting bona fide AMPAR auxiliary subunit. Shisa6 is enriched at hippocampal postsynaptic membranes and co-localizes with AMPARs. The Shisa6 C-terminus harbours a PDZ domain ligand that binds to PSD-95, constraining mobility of AMPARs in the plasma membrane and confining them to postsynaptic densities. Shisa6 expressed in HEK293 cells alters GluA1- and GluA2-mediated currents by prolonging decay times and decreasing the extent of AMPAR desensitization, while slowing the rate of recovery from desensitization. Using gene deletion, we show that Shisa6 increases rise and decay times of hippocampal CA1 miniature excitatory postsynaptic currents (mEPSCs). Shisa6-containing AMPARs show prominent sustained currents, indicating protection from full desensitization. Accordingly, Shisa6 prevents synaptically trapped AMPARs from depression at high-frequency synaptic transmission.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Electrophysiological Phenomena
  • Gene Expression Regulation / physiology
  • HEK293 Cells
  • Hippocampus / cytology
  • Hippocampus / metabolism*
  • Humans
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Mice
  • Neurons / cytology
  • Neurons / physiology*
  • Rats
  • Receptors, AMPA / genetics
  • Receptors, AMPA / metabolism*
  • Synapses
  • Two-Hybrid System Techniques

Substances

  • Membrane Proteins
  • Receptors, AMPA
  • Shisa protein, mouse