Interdisciplinary Graduate Program in Neuroscience, University of Iowa, Iowa City, Iowa, United States of America.
Iowa Neuroscience Institute, University of Iowa, Iowa City, Iowa, United States of America.
PLoS One. 2022 Mar 30;17(3):e0263197. doi: 10.1371/journal.pone.0263197. eCollection 2022.
Voltage-gated Ca2+ channels are critical for the development and mature function of the nervous system. Variants in the CACNA2D4 gene encoding the α2δ-4 auxiliary subunit of these channels are associated with neuropsychiatric and neurodevelopmental disorders. α2δ-4 is prominently expressed in the retina and is crucial for vision, but extra-retinal functions of α2δ-4 have not been investigated. Here, we sought to fill this gap by analyzing the behavioral phenotypes of α2δ-4 knockout (KO) mice. α2δ-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 α2δ-4 KO mice of both sexes were hyperactive in various assays, only females showed impaired motor coordination in the rotarod assay. α2δ-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 α2δ-4 in sensorimotor gating and motor function and identify α2δ-4 KO mice as a novel model for studying the pathophysiology associated with CACNA2D4 variants.
电压门控 Ca2+ 通道对于神经系统的发育和成熟功能至关重要。编码这些通道的辅助亚基 α2δ-4 的 CACNA2D4 基因的变异与神经精神和神经发育障碍有关。α2δ-4 在视网膜中表达丰富,对视觉至关重要,但 α2δ-4 的视网膜外功能尚未得到研究。在这里,我们通过分析 α2δ-4 敲除 (KO) 小鼠的行为表型来填补这一空白。α2δ-4 KO 小鼠(雄性和雌性)表现出明显的前脉冲抑制受损,这不太可能是由于听觉脑干反应阈值适度升高所致。虽然α2δ-4 KO 小鼠在各种测定中均表现出过度活跃,但只有雌性在转棒试验中表现出运动协调能力受损。α2δ-4 KO 小鼠在高架十字迷宫和悬尾试验中分别表现出焦虑和抗抑郁行为。我们的结果揭示了 α2δ-4 在感觉运动门控和运动功能中的意外作用,并确定 α2δ-4 KO 小鼠是研究与 CACNA2D4 变异相关的病理生理学的新型模型。