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The voltage-gated Ca(2+) channel subunit α(2)δ-4 regulates locomotor behavior and sensorimotor gating in mice

Voltage-gated Ca(2+) channels are critical for the development and mature function of the nervous system. Variants in the CACNA2D4 gene encoding the α(2)δ-4 auxiliary subunit of these channels are associated with neuropsychiatric and neurodevelopmental disorders. α(2)δ-4 is prominently expressed in...

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Detalles Bibliográficos
Autores principales: Klomp, Annette, Omichi, Ryotaro, Iwasa, Yoichiro, Smith, Richard J., Usachev, Yuriy M., Russo, Andrew F., Narayanan, Nandakumar S., Lee, Amy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8967030/
https://www.ncbi.nlm.nih.gov/pubmed/35353835
http://dx.doi.org/10.1371/journal.pone.0263197
Descripción
Sumario:Voltage-gated Ca(2+) channels are critical for the development and mature function of the nervous system. Variants in the CACNA2D4 gene encoding the α(2)δ-4 auxiliary subunit of these channels are associated with neuropsychiatric and neurodevelopmental disorders. α(2)δ-4 is prominently expressed in the retina and is crucial for vision, but extra-retinal functions of α(2)δ-4 have not been investigated. Here, we sought to fill this gap by analyzing the behavioral phenotypes of α(2)δ-4 knockout (KO) mice. α(2)δ-4 KO mice (both males and females) exhibited significant impairments in prepulse inhibition that were unlikely to result from the modestly elevated auditory brainstem response thresholds. Whereas α(2)δ-4 KO mice of both sexes were hyperactive in various assays, only females showed impaired motor coordination in the rotarod assay. α(2)δ-4 KO mice exhibited anxiolytic and anti-depressive behaviors in the elevated plus maze and tail suspension tests, respectively. Our results reveal an unexpected role for α(2)δ-4 in sensorimotor gating and motor function and identify α(2)δ-4 KO mice as a novel model for studying the pathophysiology associated with CACNA2D4 variants.