Coincidence detection in single dendritic spines mediated by calcium release

Nat Neurosci. 2000 Dec;3(12):1266-73. doi: 10.1038/81792.

Abstract

Cerebellar long-term depression (LTD) is a calcium-dependent process in which coincident activity of parallel fiber (PF) and climbing fiber (CF) synapses causes a long-lasting decrease in PF synaptic strength onto Purkinje cells. Here we show that pairing CF activation with bursts of PF activity triggers large (>10 microM) calcium signals in Purkinje cell dendrites. When PFs are densely activated, signals span whole dendritic branchlets and are mediated by voltage-dependent calcium entry. When PFs are sparsely activated, however, signals are restricted to single spines and blocked by metabotropic glutamate receptor antagonists. Single-spine signals and sparse-stimulation LTD are also blocked by thapsigargin, indicating that calcium must be released from stores. Single-spine signals and sparse-stimulation LTD are greatest when PF activation precedes the CF activation within 50-200 ms. This timing rule matches the properties of several forms of motor learning, providing a link between behavior and functional properties of cerebellar synaptic plasticity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axons / drug effects
  • Axons / metabolism
  • Axons / ultrastructure
  • Benzoates
  • Calcium Signaling / drug effects
  • Calcium Signaling / physiology*
  • Dendrites / drug effects
  • Dendrites / metabolism*
  • Dendrites / ultrastructure
  • Electric Stimulation
  • Excitatory Amino Acid Antagonists / pharmacology
  • Glycine / analogs & derivatives
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Neural Inhibition / drug effects
  • Neural Inhibition / physiology*
  • Neuronal Plasticity / drug effects
  • Neuronal Plasticity / physiology
  • Purkinje Cells / drug effects
  • Purkinje Cells / metabolism*
  • Purkinje Cells / ultrastructure
  • Quinoxalines / pharmacology
  • Rats
  • Receptors, Metabotropic Glutamate / antagonists & inhibitors
  • Synapses / drug effects
  • Synapses / metabolism*
  • Synapses / ultrastructure
  • Thapsigargin / pharmacology

Substances

  • Benzoates
  • Excitatory Amino Acid Antagonists
  • Quinoxalines
  • Receptors, Metabotropic Glutamate
  • FG 9041
  • Thapsigargin
  • 4-carboxyphenylglycine
  • Glycine