Vti1a identifies a vesicle pool that preferentially recycles at rest and maintains spontaneous neurotransmission

Neuron. 2012 Jan 12;73(1):121-34. doi: 10.1016/j.neuron.2011.10.034.

Abstract

Recent studies suggest that synaptic vesicles (SVs) giving rise to spontaneous neurotransmission are distinct from those that carry out evoked release. However, the molecular basis of this dichotomy remains unclear. Here, we focused on two noncanonical SNARE molecules, Vps10p-tail-interactor-1a (vti1a) and VAMP7, previously shown to reside on SVs. Using simultaneous multicolor imaging at individual synapses, we could show that compared to the more abundant vesicular SNARE synaptobrevin2, both vti1a and VAMP7 were reluctantly mobilized during activity. Vti1a, but not VAMP7, showed robust trafficking under resting conditions that could be partly matched by synaptobrevin2. Furthermore, loss of vti1a function selectively reduced high-frequency spontaneous neurotransmitter release detected postsynaptically. Expression of a truncated version of vti1a augmented spontaneous release more than full-length vti1a, suggesting that an autoinhibitory process regulates vti1a function. Taken together, these results support the premise that in its native form vti1a selectively maintains spontaneous neurotransmitter release.

Publication types

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

MeSH terms

  • Action Potentials / genetics
  • Anesthetics, Local / pharmacology
  • Animals
  • Animals, Newborn
  • Biological Transport / genetics
  • Biophysics
  • Calcium / metabolism
  • Cells, Cultured
  • Electric Stimulation
  • Enzyme Inhibitors / pharmacology
  • Excitatory Postsynaptic Potentials / drug effects
  • Excitatory Postsynaptic Potentials / genetics
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Hippocampus / cytology
  • Hydrogen-Ion Concentration
  • Macrolides / pharmacology
  • Microscopy, Immunoelectron / methods
  • Mutation / genetics
  • Neurons / cytology
  • Neurons / physiology*
  • Patch-Clamp Techniques
  • Potassium Chloride / pharmacology
  • Protein Transport / genetics
  • Protein Transport / physiology
  • Qb-SNARE Proteins / genetics
  • Qb-SNARE Proteins / metabolism*
  • R-SNARE Proteins / genetics
  • R-SNARE Proteins / metabolism
  • RNA, Small Interfering / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • SNARE Proteins / genetics
  • SNARE Proteins / metabolism
  • Synapses / metabolism*
  • Synapses / ultrastructure
  • Synaptic Transmission / genetics
  • Synaptic Transmission / physiology*
  • Synaptic Vesicles / genetics
  • Synaptic Vesicles / metabolism*
  • Synaptic Vesicles / ultrastructure
  • Synaptotagmin I / metabolism
  • Tetrodotoxin / pharmacology
  • Vesicle-Associated Membrane Protein 2 / metabolism

Substances

  • Anesthetics, Local
  • Enzyme Inhibitors
  • Macrolides
  • Qb-SNARE Proteins
  • R-SNARE Proteins
  • RNA, Small Interfering
  • SNARE Proteins
  • Synaptotagmin I
  • Vamp7 protein, rat
  • Vesicle-Associated Membrane Protein 2
  • Vti1a protein, rat
  • Green Fluorescent Proteins
  • Tetrodotoxin
  • Potassium Chloride
  • concanamycin A
  • Calcium