GABAergic deficits and schizophrenia-like behaviors in a mouse model carrying patient-derived neuroligin-2 R215H mutation

Mol Brain. 2018 Jun 1;11(1):31. doi: 10.1186/s13041-018-0375-6.

Abstract

Schizophrenia (SCZ) is a severe mental disorder characterized by delusion, hallucination, and cognitive deficits. We have previously identified from schizophrenia patients a loss-of-function mutation Arg215→His215 (R215H) of neuroligin 2 (NLGN2) gene, which encodes a cell adhesion molecule critical for GABAergic synapse formation and function. Here, we generated a novel transgenic mouse line with neuroligin-2 (NL2) R215H mutation. The single point mutation caused a significant loss of NL2 protein in vivo, reduced GABAergic transmission, and impaired hippocampal activation. Importantly, R215H KI mice displayed anxiety-like behavior, impaired pre-pulse inhibition (PPI), cognition deficits and abnormal stress responses, recapitulating several key aspects of schizophrenia-like behaviors. Our results demonstrate a significant impact of a single point mutation NL2 R215H on brain functions, providing a novel animal model for the study of schizophrenia and neuropsychiatric disorders.

Keywords: GABA; Mouse model; Mutation; Neuroligin-2; Schizophrenia.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Behavior, Animal*
  • Cell Adhesion Molecules, Neuronal / genetics*
  • Disease Models, Animal
  • Hippocampus / metabolism
  • Humans
  • Mice, Transgenic
  • Mutation / genetics*
  • Nerve Tissue Proteins / genetics*
  • Neurons / metabolism
  • Schizophrenia / genetics*
  • Schizophrenia / pathology*
  • Stress, Physiological
  • Synapses / metabolism
  • Synaptic Transmission
  • gamma-Aminobutyric Acid / metabolism*

Substances

  • Cell Adhesion Molecules, Neuronal
  • Nerve Tissue Proteins
  • neuroligin 2
  • gamma-Aminobutyric Acid