Mutations of CNTNAP1 led to defects in neuronal development

• Published in: JCI insight Vol. 5; no. 21
• Main Authors: Li, Wanxing, Yang, Lin, Tang, Chuanqing, Liu, Kaiyi, Lu, Yulan, Wang, Huijun, Yan, Kai, Qiu, Zilong, Zhou, Wenhao
• Format: Journal Article
• Language: English
• Published: United States American Society for Clinical Investigation 05.11.2020; American Society for Clinical investigation
• Subjects: Genetics; Neuroscience; Neurodevelopment; Genetics; Neuroscience
• ISSN: 2379-3708; 2379-3708
• DOI: 10.1172/jci.insight.135697

Mutations of CNTNAP1 were associated with myelination disorders, suggesting the role of CNTNAP1 in myelination processes. Whether CNTNAP1 may have a role in early cortical neuronal development is largely unknown. In this study, we identified 4 compound heterozygous mutations of CNTNAP1 in 2 Chinese families. Using mouse models, we found that CNTNAP1 is highly expressed in neurons and is located predominantly in MAP2+ neurons during the early developmental stage. Importantly, Cntnap1 deficiency results in aberrant dendritic growth and spine development in vitro and in vivo, and it delayed migration of cortical neurons during early development. Finally, we found that the number of parvalbumin+ neurons in the cortex and hippocampus of Cntnap1-/- mice is strikingly increased by P15, suggesting that excitation/inhibition balance is impaired. Together, this evidence elucidates a critical function of CNTNAP1 in cortical development, providing insights underlying molecular and circuit mechanisms of CNTNAP1-related disease.