A subtype-specific function for the extracellular domain of neuroligin 1 in hippocampal LTP

Neuron. 2012 Oct 18;76(2):309-16. doi: 10.1016/j.neuron.2012.07.024. Epub 2012 Oct 17.

Abstract

At neuronal excitatory synapses, two major subtypes of the synaptic adhesion molecule neuroligin are present. These subtypes, neuroligin 1 and neuroligin 3, have roles in synaptogenesis and synaptic maintenance that appear largely overlapping. In this study, we combine electrophysiology with molecular deletion and replacement of these proteins to identify similarities and differences between these subtypes. In doing so, we identify a subtype-specific role in LTP for neuroligin 1 in young CA1, which persists into adulthood in the dentate gyrus. As neuroligin 3 showed no requirement for LTP, we constructed chimeric proteins of the two excitatory neuroligin subtypes to identify the molecular determinants particular to the unique function of neuroligin 1. Using in vivo molecular replacement experiments, we find that these unique functions depend on a region in its extracellular domain containing the B site splice insertion previously shown to determine specificity of neurexin binding.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Animals
  • Animals, Newborn
  • Biophysics
  • Cell Adhesion Molecules, Neuronal / chemistry
  • Cell Adhesion Molecules, Neuronal / genetics
  • Cell Adhesion Molecules, Neuronal / physiology*
  • Cell Line, Transformed
  • Dendritic Spines / genetics
  • Dendritic Spines / metabolism
  • Electric Stimulation
  • Excitatory Amino Acid Agonists / pharmacology
  • Excitatory Amino Acid Antagonists / pharmacology
  • Green Fluorescent Proteins / genetics
  • Hippocampus / cytology*
  • Hippocampus / physiology*
  • Humans
  • Long-Term Potentiation / drug effects
  • Long-Term Potentiation / genetics*
  • Membrane Proteins / chemistry
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology*
  • MicroRNAs / genetics
  • MicroRNAs / metabolism
  • N-Methylaspartate / pharmacology
  • Nerve Tissue Proteins / chemistry
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / physiology*
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / physiology*
  • Organ Culture Techniques
  • Patch-Clamp Techniques
  • Protein Structure, Tertiary / physiology
  • Quinoxalines / pharmacology
  • RNA Interference / physiology
  • Rats
  • Statistics, Nonparametric
  • Stereotaxic Techniques
  • Transduction, Genetic
  • Transfection
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid / pharmacology

Substances

  • Cell Adhesion Molecules, Neuronal
  • Excitatory Amino Acid Agonists
  • Excitatory Amino Acid Antagonists
  • Membrane Proteins
  • MicroRNAs
  • Nerve Tissue Proteins
  • Quinoxalines
  • neuroligin 1
  • neuroligin 3
  • 2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline
  • Green Fluorescent Proteins
  • N-Methylaspartate
  • alpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic Acid