Blocking endocytosis enhances short-term synaptic depression under conditions of normal availability of vesicles

Neuron. 2013 Oct 16;80(2):343-9. doi: 10.1016/j.neuron.2013.08.010.

Abstract

It is commonly thought that clathrin-mediated endocytosis is the rate-limiting step of synaptic transmission in small CNS boutons with limited capacity for synaptic vesicles, causing short-term depression during high rates of synaptic transmission. Here, we show by analyzing synaptopHluorin fluorescence that 200 action potentials evoke the same cumulative amount of vesicle fusion, irrespective of the frequency of stimulation (5-40 Hz), implying the absence of vesicle reuse, since the method used (alkaline-trapping) measures only first-round exocytosis. After blocking all slow or specifically clathrin-mediated endocytosis, however, the same stimulation patterns cause a rapid stimulation-frequency-dependent release depression. This form of depression does not reflect insufficient vesicle supply, but appears to be the result of slow clearance of vesicular components from the release site. Our findings uncover an important yet overlooked role of endocytic proteins for release site clearance in addition to their well-characterized role in endocytosis itself.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / physiology
  • Animals
  • Electric Stimulation
  • Endocytosis / drug effects
  • Endocytosis / physiology*
  • Hippocampus / metabolism
  • Hippocampus / physiology
  • Hydrazones / pharmacology
  • Neurons / metabolism
  • Neurons / physiology*
  • Primary Cell Culture
  • Rats
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology*
  • Synaptic Vesicles / metabolism*

Substances

  • Adaptor Proteins, Vesicular Transport
  • Hydrazones
  • N'-(3,4-dihydroxybenzylidene)-3-hydroxy-2-naphthahydrazide