Environmental Enrichment Rescues Social Behavioral Deficits and Synaptic Abnormalities in Pten Haploinsufficient Mice

Genes (Basel). 2021 Aug 30;12(9):1366. doi: 10.3390/genes12091366.

Abstract

Pten germline haploinsufficient (Pten+/-) mice, which model macrocephaly/autism syndrome, show social and repetitive behavior deficits, early brain overgrowth, and cortical-subcortical hyperconnectivity. Previous work indicated that altered neuronal connectivity may be a substrate for behavioral deficits. We hypothesized that exposing Pten+/- mice to environmental enrichment after brain overgrowth has occurred may facilitate adaptation to abnormal "hard-wired" connectivity through enhancing synaptic plasticity. Thus, we reared Pten+/- mice and their wild-type littermates from weaning under either standard (4-5 mice per standard-sized cage, containing only bedding and nestlet) or enriched (9-10 mice per large-sized cage, containing objects for exploration and a running wheel, plus bedding and nestlet) conditions. Adult mice were tested on social and non-social assays in which Pten+/- mice display deficits. Environmental enrichment rescued sex-specific deficits in social behavior in Pten+/- mice and partially rescued increased repetitive behavior in Pten+/- males. We found that Pten+/- mice show increased excitatory and decreased inhibitory pre-synaptic proteins; this phenotype was also rescued by environmental enrichment. Together, our results indicate that environmental enrichment can rescue social behavioral deficits in Pten+/- mice, possibly through normalizing the excitatory synaptic protein abundance.

Keywords: Pten; autism; environmental enrichment; neurodevelopment; synaptic plasticity.

Publication types

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

MeSH terms

  • Animals
  • Autistic Disorder / etiology
  • Behavior, Animal / physiology*
  • Brain / abnormalities
  • Brain / pathology
  • Disease Models, Animal
  • Facies
  • Female
  • Haploinsufficiency
  • Male
  • Megalencephaly / etiology
  • Mice
  • Mice, Inbred C57BL
  • Mice, Mutant Strains
  • PTEN Phosphohydrolase / genetics*
  • Social Behavior*
  • Synapses / pathology*

Substances

  • PTEN Phosphohydrolase
  • Pten protein, mouse

Supplementary concepts

  • Macrocephaly Autism Syndrome