Taugher-Hebl R J, Berns A, Jones M, Townsend A, Eagen A K, Ferri Sarah L, Langbehn D R, Janouschek H
Department of Psychiatry, Iowa Neuroscience Institute, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.
Department of Veterans Affairs Medical Center, Iowa City, Iowa, USA.
Autism Res. 2025 May;18(5):1011-1023. doi: 10.1002/aur.70034. Epub 2025 Apr 17.
The contactin-associated protein-like 2 (Cntnap2) gene is relevant to autism spectrum disorder (ASD), which is associated with age-specific structural alterations in limbic brain regions. The Cntnap2 gene encodes for the contactin-associated protein-like 2 (CASPR2) protein, and CASPR2 protein levels are high in the amygdala, a limbic region that is essential for the processing of fear and anxiety. In humans, reduced levels of this protein arising from CNTNAP2 mutations could potentially account for the autism-associated increase in fear and anxiety. Here, we report the extent to which loss of CASPR2 in mice contributes to the development of fear- and anxiety-related behaviors. Pavlovian fear conditioning experiments revealed that loss of CASPR2 has age-dependent effects on the acquisition of fear memory, recall of both cue-evoked and context-related fear memory, and stability of cue-evoked fear memory. Additionally, data from the elevated zero maze suggest that CASPR2 deficiency contributes to anxiety-related behaviors, especially in juvenile (29-day old) mice. These are the first reports of age-dependent effects of CASPR2 deficiency on fear and anxiety-related behaviors, and they set the stage for a better understanding of developmental alterations of fear and anxiety in ASD.
接触蛋白相关蛋白样2(Cntnap2)基因与自闭症谱系障碍(ASD)相关,而自闭症谱系障碍与边缘脑区特定年龄的结构改变有关。Cntnap2基因编码接触蛋白相关蛋白样2(CASPR2)蛋白,且杏仁核中CASPR2蛋白水平较高,杏仁核是边缘系统的一个区域,对恐惧和焦虑的处理至关重要。在人类中,由CNTNAP2突变导致的这种蛋白水平降低可能是自闭症相关的恐惧和焦虑增加的原因。在此,我们报告了小鼠中CASPR2缺失对恐惧和焦虑相关行为发展的影响程度。经典条件恐惧实验表明,CASPR2缺失对恐惧记忆的获得、线索诱发和情境相关恐惧记忆的回忆以及线索诱发恐惧记忆的稳定性具有年龄依赖性影响。此外,高架零迷宫实验数据表明,CASPR2缺陷会导致焦虑相关行为,尤其是在幼年(29日龄)小鼠中。这些是关于CASPR2缺陷对恐惧和焦虑相关行为的年龄依赖性影响的首次报道,为更好地理解自闭症中恐惧和焦虑的发育改变奠定了基础。