4.7 Article

ASD/OCD-Linked Protocadherin-10 Regulates Synapse, But Not Axon, Development in the Amygdala and Contributes to Fear- and Anxiety-Related Behaviors

期刊

JOURNAL OF NEUROSCIENCE
卷 42, 期 21, 页码 4250-4266

出版社

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.1843-21.2022

关键词

autism spectrum disorder; basolateral nucleus of the amygdala; fear and anxiety; obsessive-compulsive disor-der; PCDH10; synapse development

资金

  1. National Institutes of Health (NIH)/National Institute on Drug Abuse [DA042744]
  2. NIH/National Institute of Mental Health [MH125162]
  3. Simons Foundation Autism Research Initiative (SFARI) [568285]
  4. Uehara Memorial Foundation

向作者/读者索取更多资源

This study reveals the critical role of PCDH10 in excitatory synapse development in the dorsal amygdala and its regulation of anxiety-related, fear-related, and stress-related behaviors.
The Protocadherin-10 (PCDH10) gene is associated with autism spectrum disorder (ASD), obsessive-compulsive disorder (OCD), and major depression (MD). The PCDH10 protein is a homophilic cell adhesion molecule that belongs to the d2-pro-tocadherin family. PCDH10 is highly expressed in the developing brain, especially in the basolateral nucleus of the amygdala (BLA). However, the role of PCDH10 in vivo has been debatable: one paper reported that a Pcdh10 mutant mouse line showed changes in axonal projections; however, another Pcdh10 mutant mouse line was reported to have failed to detect axo-nal phenotypes. Therefore, the actual roles of PCDH10 in the brain remain to be elucidated. We established a new Pcdh10 KO mouse line using the CRISPR/Cas9 system, without inserting gene cassettes to avoid nonspecific effects, examined the roles of PCDH10 in the brain, and studied the behavioral consequences of Pcdh10 inactivation. Here, we show that Pcdh10 KO mice do not show defects in axonal development. Instead, we find that Pcdh10 KO mice exhibit impaired development of excitatory synapses in the dorsal BLA. We further demonstrate that male Pcdh10 KO mice exhibit reduced anxiety-related behaviors, impaired fear conditioning, decreased stress-coping responses, and mildly impaired social recognition and commu-nication. These results indicate that PCDH10 plays a critical role in excitatory synapse development, but not axon develop-ment, in the dorsal BLA and that PCDH10 regulates anxiety-related, fear-related, and stress-related behaviors. Our results reveal the roles of PCDH10 in the brain and its relationship to relevant psychiatric disorders such as ASD, OCD, and MD.

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