Tumor necrosis factor-alpha-induced neutral sphingomyelinase-2 modulates synaptic plasticity by controlling the membrane insertion of NMDA receptors

J Neurochem. 2009 Jun;109(5):1237-49. doi: 10.1111/j.1471-4159.2009.06038.x. Epub 2009 Mar 14.

Abstract

The insertion and removal of NMDA receptors from the synapse are critical events that modulate synaptic plasticity. While a great deal of progress has been made on understanding the mechanisms that modulate trafficking of NMDA receptors, we do not currently understand the molecular events required for the fusion of receptor containing vesicles with the plasma membrane. Here, we show that sphingomyelin phosphodiesterase 3 (also known as neutral sphingomyelinase-2) is critical for tumor necrosis factor (TNF) alpha-induced trafficking of NMDA receptors and synaptic plasticity. TNFalpha initiated a rapid increase in ceramide that was associated with increased surface localization of NMDA receptor NR1 subunits and a specific clustering of NR1 phosphorylated on serines 896 and 897 into lipid rafts. Brief applications of TNFalpha increased the rate and amplitude of NMDA-evoked calcium bursts and enhanced excitatory post-synaptic currents. Pharmacological inhibition or genetic mutation of neutral sphingomyelinase-2 prevented TNFalpha-induced generation of ceramide, phosphorylation of NR1 subunits, clustering of NR1, enhancement of NMDA-evoked calcium flux and excitatory post-synaptic currents.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural

MeSH terms

  • Aniline Compounds / pharmacology
  • Animals
  • Benzylidene Compounds / pharmacology
  • Calcium / metabolism
  • Cells, Cultured
  • Ceramides / metabolism
  • Embryo, Mammalian
  • Enzyme Inhibitors / pharmacology
  • Excitatory Postsynaptic Potentials / drug effects
  • Excitatory Postsynaptic Potentials / physiology
  • Fatty Acids, Monounsaturated / pharmacology
  • Fluorescence Resonance Energy Transfer / methods
  • Gangliosidosis, GM1 / metabolism
  • Hippocampus / cytology
  • In Vitro Techniques
  • Membrane Microdomains / drug effects
  • Membrane Microdomains / metabolism
  • Mutation / physiology
  • Neuronal Plasticity / drug effects
  • Neuronal Plasticity / physiology*
  • Neurons / drug effects*
  • Patch-Clamp Techniques / methods
  • Phosphorylation / drug effects
  • Protein Transport / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, N-Methyl-D-Aspartate / metabolism*
  • Serine / metabolism
  • Spectrometry, Mass, Electrospray Ionization / methods
  • Sphingomyelin Phosphodiesterase / genetics
  • Sphingomyelin Phosphodiesterase / metabolism*
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Aniline Compounds
  • Benzylidene Compounds
  • Ceramides
  • Enzyme Inhibitors
  • Fatty Acids, Monounsaturated
  • GW 4869
  • NR1 NMDA receptor
  • Receptors, N-Methyl-D-Aspartate
  • Tumor Necrosis Factor-alpha
  • Serine
  • Smpd3 protein, rat
  • Sphingomyelin Phosphodiesterase
  • Calcium
  • thermozymocidin