AMPA receptor-dependent clustering of synaptic NMDA receptors is mediated by Stargazin and NR2A/B in spinal neurons and hippocampal interneurons

Neuron. 2004 Oct 14;44(2):335-49. doi: 10.1016/j.neuron.2004.09.029.

Abstract

Under standard conditions, cultured ventral spinal neurons cluster AMPA- but not NMDA-type glutamate receptors at excitatory synapses on their dendritic shafts in spite of abundant expression of the ubiquitous NMDA receptor subunit NR1. We demonstrate here that the NMDA receptor subunits NR2A and NR2B are not routinely expressed in cultured spinal neurons and that transfection with NR2A or NR2B reconstitutes the synaptic targeting of NMDA receptors and confers on exogenous application of the immediate early gene product Narp the ability to cluster both AMPA and NMDA receptors. The use of dominant-negative mutants of GluR2 further showed that the synaptic targeting of NMDA receptors is dependent on the presence of synaptic AMPA receptors and that synaptic AMPA and NMDA receptors are linked by Stargazin and a MAGUK protein. This system of AMPA receptor-dependent synaptic NMDA receptor localization was preserved in hippocampal interneurons but reversed in hippocampal pyramidal neurons.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Blotting, Northern
  • C-Reactive Protein / physiology
  • Calcium Channels / physiology*
  • Cells, Cultured
  • Guanylate Kinases
  • Hippocampus / physiology
  • Humans
  • Immunohistochemistry
  • Nerve Tissue Proteins / physiology
  • Neurons / physiology*
  • Nucleoside-Phosphate Kinase / physiology
  • Protein Subunits / physiology
  • Rats
  • Receptors, AMPA / physiology*
  • Receptors, N-Methyl-D-Aspartate / physiology*
  • Spinal Cord / physiology
  • Synapses / physiology*
  • Transfection

Substances

  • Cacng2 protein, rat
  • Calcium Channels
  • Nerve Tissue Proteins
  • Protein Subunits
  • Receptors, AMPA
  • Receptors, N-Methyl-D-Aspartate
  • neuronal pentraxin
  • C-Reactive Protein
  • Nucleoside-Phosphate Kinase
  • Guanylate Kinases