
Loss of the autism spectrum disorder risk gene Cntnap2 leads to increased intrinsic excitability of striatal projection neurons, particularly in the direct pathway, which contributes to the manifestation of repetitive behaviors and cognitive inflexibility in mice.


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Autism spectrum disorder (ASD) is a neurodevelopmental disorder characterized by two major diagnostic criteria - persistent deficits in social communication and interaction, and the presence of restricted, repetitive patterns of behavior (RRBs). Evidence from both human and animal model studies of ASD suggest that alteration of striatal circuits, which mediate motor learning, action selection, and habit formation, may contribute to the manifestation of RRBs. CNTNAP2 is a syndromic ASD risk gene, and loss of function of Cntnap2 in mice is associated with RRBs. How loss of Cntnap2 impacts striatal neuron function is largely unknown. In this study, we utilized Cntnap2-/- mice to test whether altered striatal neuron activity contributes to aberrant motor behaviors relevant to ASD. We find that Cntnap2-/- mice exhibit increased cortical drive of striatal projection neurons (SPNs), with the most pronounced effects in direct pathway SPNs. This enhanced drive is likely due to increased intrinsic excitability of SPNs, which make them more responsive to cortical inputs. We also find that Cntnap2-/- mice exhibit spontaneous repetitive behaviors, increased motor routine learning, and cognitive inflexibility. Increased corticostriatal drive, in particular of the direct pathway, may contribute to the acquisition of repetitive, inflexible behaviors in Cntnap2 mice.

### Competing Interest Statement

The authors have declared no competing interest.

Cntnap2 loss drives striatal neuron hyperexcitability and behavioral inflexibility

loss-of-cntnap2-leads-to-striatal-neuron-hyperexcitability-and-behavioral-inflexibility-in-mice


Loss of Cntnap2 Leads to Striatal Neuron Hyperexcitability and Behavioral Inflexibility in Mice
