Abstract
BACKGROUND: Mental disorders are common in the United States. According to the National Institute of Mental Health more than 23% of the adult population in the United States live with some form of mental illness. Genome-wide association studies have implicated CACNA1C, which encodes the L-type voltage-gated calcium channel Ca(V)1.2, and it has been suggested that the expression levels of CACNA1C may be associated with mental illness. To this end, we have generated a novel mouse line that conditionally overexpresses the mouse ortholog Cacna1c. METHODS: Transgenic mice (Ca(V)1.2(Tg+) mice) were characterized for expression and distribution of Ca(V)1.2. The Ca(V)1.2(Tg+) mice were compared with control littermates using assays that examined cognitive and affective behaviors. Cortical network dynamics were assessed using in vivo multiphoton calcium imaging. RESULTS: Compared with their control littermates, Ca(V)1.2(Tg+) mice exhibited a ∼1-fold increase in Ca(V)1.2 expression. Behavioral characterization of the Ca(V)1.2(Tg+) mice revealed a complex phenotype in which they exhibited deficits in the consolidation of fearful memories and an increase in anxiolytic-like behavior. The Ca(V)1.2(Tg+) mice also appeared to have altered cortical dynamics in which the network was more dense but less synchronized. CONCLUSIONS: We have successfully generated mice that overexpress the mouse ortholog of a gene that has been implicated in several psychiatric diseases. Our initial characterization suggests that these mice have alterations in behavior and neural function that have been linked to mental illness. It is anticipated that future studies will reveal additional neurobehavioral alterations whose mechanisms will be studied.