Postsynaptic protein mobility in dendritic spines: long-term regulation by synaptic NMDA receptor activation

Mol Cell Neurosci. 2006 Apr;31(4):702-12. doi: 10.1016/j.mcn.2006.01.010. Epub 2006 Feb 28.


Reorganization of molecular components represents a cellular mechanism for synaptic plasticity. Dendritic spines, major sites for glutamatergic synapses, compartmentalize dynamic changes in molecular composition. Here, we use fluorescence recovery after photobleaching (FRAP) in cultured hippocampal neurons to show that spine proteins undergo continual exchange with extra-spine pools. Each spine component has a distinctive mobility: calcium/calmodulin activated protein kinase CaMKIIalpha > GluR1 AMPA glutamate receptor > PSD-95 scaffolding protein > NR1 NMDA glutamate receptor. Stimulation of synaptic NMDA receptors by a protocol that induces chemical LTP resulted in a long-lasting reduction in the mobility of spine CaMKIIalpha and an increased mobile fraction but slower kinetics for spine GluR1. Stimulation also increased the resistance of postsynaptic CaMKIIalpha to detergent extraction. These results suggest long-lasting changes in affinity of protein-protein interactions and/or ongoing alterations in exo/endocytosis. Such lasting changes in protein mobility may contribute to maintaining alterations in synaptic efficacy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Cells, Cultured
  • Dendritic Spines / chemistry
  • Dendritic Spines / metabolism*
  • Disks Large Homolog 4 Protein
  • Hippocampus / cytology
  • Intracellular Signaling Peptides and Proteins / metabolism
  • Long-Term Potentiation / physiology
  • Membrane Proteins / metabolism
  • Nerve Tissue Proteins / metabolism
  • Neurons / chemistry
  • Neurons / cytology
  • Neurons / metabolism*
  • Rats
  • Receptors, AMPA / metabolism
  • Receptors, N-Methyl-D-Aspartate / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Synapses / chemistry
  • Synapses / physiology*


  • Disks Large Homolog 4 Protein
  • Dlg4 protein, rat
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • NR1 NMDA receptor
  • Nerve Tissue Proteins
  • Receptors, AMPA
  • Receptors, N-Methyl-D-Aspartate
  • Recombinant Fusion Proteins
  • postsynaptic density proteins
  • Calcium-Calmodulin-Dependent Protein Kinase Type 2
  • Calcium-Calmodulin-Dependent Protein Kinases
  • glutamate receptor ionotropic, AMPA 1