Age dependent impairment of home cage behavior and reactivity in Cntnap2 knock out mouse model

Contactin-associated protein-like 2 (CNTNAP2) is a transmembrane protein that mediates neuron-glia interactions and regulates dendritic spine growth and neuronal migration. Mutations in the CNTNAP2 gene are linked to autism and epilepsy. Younger Cntnap2 KO mice mimic autism phenotypes, while older mice are a model for epilepsy. Thus, comparing behavioral phenotypes across different ages is needed to better understand the age dependent development of disordered brain networks in Cntnap2 mutants. Male and female Cntnap2 KO and WT controls were tested across different age groups (4, 5, 7, 9, and ∼11 months) using digging, stimulus (reactivity), and nesting assays. Older Cntnap2 KO mice (7, 9, and ∼11 months) showed a significant increase in home cage reactivity (stimulus) assay compared to younger mice at 4 and 5 months of age. Similar trends were observed in male and female Cntnap2 KO mice. No significant differences were observed in WT controls. A significant difference in digging assay was observed in KO female mice between younger (4 month) and older mice post nest removal. An age-dependent significant reduction in nesting behavior was observed in female KO mice; however, no difference was observed in the WT controls. Immunohistochemical analysis showed age dependent change interneuron and microglial network in Cntnap2 KO mice. Our findings suggest disruption in home cage behavior and reactivity in older pre-epileptic Cntnap2 KO mice indicating an age-dependent network alteration and behavior deficits.

This study investigates the age-dependent behavioral changes in Cntnap2 KO mice due to underlying changes in the neuronal network. It has been shown that younger Cntnap2 KO mice display autistic behaviors and that older Cntnap2 KO mice have epilepsy, but it is unknown how behavior is affected during the intervening period of epileptogenesis. We find that female Cntnap2 KO mice at 11 months of age have increased reactivity and decreased motor activity compared to younger age groups, whereas WT mice show no relationship between age and behavior. Overall, the loss of Cntnap2 alters behavior in an age-dependent and sex-specific manner, indicating progressive dysregulation of the neuronal network.