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.

Highlights

  • A subset of individuals with autism spectrum disorder (ASD) display overgrowth of the head and brain

  • Up to 25% of these cases are classified as macrocephaly/autism syndrome (OMIM #605309), which is caused by mutations in the Phosphatase and tensin homolog (PTEN) gene [1,2,3,4,5,6,7]

  • We have previously examined macrocephaly/autism syndrome using mice with germline Pten haploinsufficiency (Pten+/−), which are a model for the PTEN mutations found in humans with macrocephaly/autism syndrome

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Summary

Introduction

A subset of individuals with autism spectrum disorder (ASD) display overgrowth of the head (macrocephaly) and brain (megalencephaly). We have previously examined macrocephaly/autism syndrome using mice with germline Pten haploinsufficiency (Pten+/−), which are a model for the PTEN mutations found in humans with macrocephaly/autism syndrome These mice have abnormal social and non-social behavior [14,15,16,17] on tests related to the core symptoms of ASD (social behavior and communication deficits, and restricted, repetitive behavior and interests [18]). These mice exhibit cortical–subcortical hyperconnectivity, and brain overgrowth that is present from birth and persists into adulthood; this overgrowth is primarily due to hyperplasia, and to hypertrophy in a subset of neuronal cell types [14,17,19,20,21,22]

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