Pre-post synaptic alignment through neuroligin-1 tunes synaptic transmission efficiency

Elife. 2018 Jul 25:7:e31755. doi: 10.7554/eLife.31755.

Abstract

The nanoscale organization of neurotransmitter receptors regarding pre-synaptic release sites is a fundamental determinant of the synaptic transmission amplitude and reliability. How modifications in the pre- and post-synaptic machinery alignments affects synaptic currents, has only been addressed with computer modelling. Using single molecule super-resolution microscopy, we found a strong spatial correlation between AMPA receptor (AMPAR) nanodomains and the post-synaptic adhesion protein neuroligin-1 (NLG1). Expression of a truncated form of NLG1 disrupted this correlation without affecting the intrinsic AMPAR organization, shifting the pre-synaptic release machinery away from AMPAR nanodomains. Electrophysiology in dissociated and organotypic hippocampal rodent cultures shows these treatments significantly decrease AMPAR-mediated miniature and EPSC amplitudes. Computer modelling predicts that ~100 nm lateral shift between AMPAR nanoclusters and glutamate release sites induces a significant reduction in AMPAR-mediated currents. Thus, our results suggest the synapses necessity to release glutamate precisely in front of AMPAR nanodomains, to maintain a high synaptic responses efficiency.

Keywords: AMPA receptors; neuroscience; rat; super-resolution microscopy; synaptic transmission.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules, Neuronal / genetics
  • Cell Adhesion Molecules, Neuronal / metabolism*
  • Cells, Cultured
  • Excitatory Postsynaptic Potentials
  • Female
  • Hippocampus / cytology
  • Hippocampus / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mutation
  • Neurons / cytology
  • Neurons / metabolism*
  • Rats
  • Receptors, AMPA / metabolism*
  • Synapses / physiology*
  • Synaptic Transmission

Substances

  • Cell Adhesion Molecules, Neuronal
  • Receptors, AMPA
  • neuroligin 1