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The Impact of Overexpression of the Mouse Ortholog of CACNA1C on Behavior and Cortical Dynamics

  • Rachel Parent
  • , Ruei Lung Lin
  • , Lara Ouillette
  • , Emily Glass
  • , Hannah Burns
  • , Michael D. Uhler
  • , Sami L. Case
  • , Olivier Thibault
  • , Geoffrey G. Murphy

Research output: Contribution to journalArticlepeer-review

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 CaV1.2, 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 (CaV1.2Tg+ mice) were characterized for expression and distribution of CaV1.2. The CaV1.2Tg+ 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, CaV1.2Tg+ mice exhibited a ∼1-fold increase in CaV1.2 expression. Behavioral characterization of the CaV1.2Tg+ mice revealed a complex phenotype in which they exhibited deficits in the consolidation of fearful memories and an increase in anxiolytic-like behavior. The CaV1.2Tg+ 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.

Original languageEnglish
Article number100537
JournalBiological Psychiatry Global Open Science
Volume5
Issue number5
DOIs
StatePublished - Sep 2025

Bibliographical note

Publisher Copyright:
© 2025 The Authors

Funding

This work was supported in part by an award from the Pritzker Neuropsychiatric Disorders Research Consortium (to GGM) and the National Institutes of Health (Grant Nos. R01AG074552 and R01AG081981R01 [to GGM]; R01AG058171 [to GGM and OT]; and P01AG078116 [to OT]). RP and GGM were responsible for conceptualization. RP was responsible for methodology. MDU was responsible for validation. RP, GGM, R-LL, and OT were responsible for formal analysis. RP, LO, HB, SLC, and R-LL were responsible for investigation. RP and GGM were responsible for writing the original draft of the article. GGM and OT were responsible for supervision. GGM was responsible for project administration. GGM and OT were responsible for funding acquisition. All authors read and approved the submitted version of the article. We thank the University of Michigan Transgenic Animal Model Core. We thank and acknowledge the help from Austin T. Smarsh. Some of the data herein have been published in abstract form. The authors report no biomedical financial interests or potential conflicts of interest. This work was supported in part by an award from the Pritzker Neuropsychiatric Disorders Research Consortium (to GGM) and the National Institutes of Health (Grant Nos. R01AG074552 and R01AG081981R01 [to GGM]; R01AG058171 [to GGM and OT]; and P01AG078116 [to OT]).

FundersFunder number
Michigan Diabetes Research Center, University of Michigan
National Institutes of Health (NIH)R01AG074552, R01AG081981R01, R01AG058171, P01AG078116

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Bipolar disorder
    • Cortical subnetworks
    • L-type calcium channel Ca1.2
    • Psychiatric risk variant
    • Schizophrenia

    ASJC Scopus subject areas

    • Psychiatric Mental Health
    • Clinical Neurology
    • Psychiatry and Mental health
    • Biological Psychiatry

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