Decreased NR2B subunit synaptic levels cause impaired long-term potentiation but not long-term depression

J Neurosci. 2009 Jan 21;29(3):669-77. doi: 10.1523/JNEUROSCI.3921-08.2009.

Abstract

The discovery of the molecular mechanisms regulating the abundance of synaptic NMDA receptors is essential for understanding how synaptic plasticity, as well as excitotoxic events, are regulated. However, a complete understanding of the precise molecular mechanisms regulating the composition of the NMDA receptor complex at hippocampal synapse is still missing. Here, we show that 2 h of CaMKII inhibition leads to a specific reduction of synaptic NR2B-containing NMDA receptors without affecting localization of the NR2A subunit; this molecular event is accompanied by a dramatic reduction in the induction of long-term potentiation (LTP), while long-term depression induction is unaffected. The same molecular and functional results were obtained by disrupting NR2B/PSD-95 complex with NR2B C-tail cell permeable peptide (TAT-2B). These data indicate that NR2B redistribution between synaptic and extrasynaptic membranes represents an important molecular disturbance of the glutamatergic synapse and affects the correct induction of LTP.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • CREB-Binding Protein / metabolism
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2 / metabolism
  • Cells, Cultured
  • Disks Large Homolog 4 Protein
  • Electric Stimulation
  • Embryo, Mammalian
  • Enzyme Inhibitors / pharmacology
  • Enzyme-Linked Immunosorbent Assay / methods
  • Hippocampus / cytology
  • Immunoprecipitation
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Long-Term Potentiation / drug effects
  • Long-Term Potentiation / physiology*
  • Long-Term Synaptic Depression / drug effects
  • Long-Term Synaptic Depression / physiology*
  • Membrane Proteins / metabolism
  • Neurons / cytology*
  • Neurons / drug effects
  • Neurons / physiology*
  • Organ Culture Techniques
  • Patch-Clamp Techniques
  • Peptides / pharmacology
  • Protein Transport / drug effects
  • Rats
  • Receptors, N-Methyl-D-Aspartate / metabolism*
  • Subcellular Fractions / metabolism
  • Synapses / drug effects
  • Synapses / metabolism*
  • Time Factors

Substances

  • CaMKII inhibitor AIP
  • Disks Large Homolog 4 Protein
  • Dlg4 protein, rat
  • Enzyme Inhibitors
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • NR2B NMDA receptor
  • Peptides
  • Receptors, N-Methyl-D-Aspartate
  • CREB-Binding Protein
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2