Munc13-3 superprimes synaptic vesicles at granule cell-to-basket cell synapses in the mouse cerebellum

J Neurosci. 2014 Oct 29;34(44):14687-96. doi: 10.1523/JNEUROSCI.2060-14.2014.

Abstract

Munc13-3 is a presynaptic protein implicated in vesicle priming that is strongly expressed in cerebellar granule cells (GCs). Mice deficient of Munc13-3 (Munc13-3(-/-)) show an increased paired-pulse ratio (PPR), which led to the hypothesis that Munc13-3 increases the release probability (pr) of vesicles. In the present study, we analyzed unitary synaptic connections between GCs and basket cells in acute cerebellar slices from wild-type and Munc13-3(-/-) mice. Unitary EPSCs recorded from Munc13-3(-/-) GCs showed normal kinetics and synaptic latency but a significantly increased PPR and fraction of synaptic failures. A quantal analysis revealed that neither the charge of single quanta nor the binominal parameter N were affected by loss of Munc13-3 but that pr was almost halved in Munc13-3(-/-). Neither presynaptic Ca(2+) influx was affected by deletion of Munc13-3 nor replenishment of the readily releasable vesicle pool. However, a high concentration of EGTA led to a reduction in EPSCs that was significantly stronger in Munc13-3(-/-). We conclude that Munc13-3 is responsible for an additional step of molecular and/or positional "superpriming" that substantially increases the efficacy of Ca(2+)-triggered release.

Keywords: Munc13; granule cell; release probability; superpriming; vesicular release.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calcium / metabolism
  • Cerebellum / metabolism*
  • Excitatory Postsynaptic Potentials / physiology
  • Mice
  • Nerve Tissue Proteins / metabolism*
  • Neurons / metabolism*
  • Synapses / metabolism*
  • Synaptic Transmission / physiology
  • Synaptic Vesicles / metabolism*

Substances

  • Nerve Tissue Proteins
  • Unc13c protein, mouse
  • Calcium