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Function of the synaptic cell adhesion protein neurexin-3 in human neurons

Subject Area Experimental Models for the Understanding of Nervous System Diseases
Molecular Biology and Physiology of Neurons and Glial Cells
Molecular and Cellular Neurology and Neuropathology
Term from 2021 to 2023
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 458054460
 
Final Report Year 2024

Final Report Abstract

Our study aimed to dissect the role of neurexin (NRXN) genes in neuronal development and synaptic transmission. Mutations in these synaptic proteins are associated with neuropsychiatric disorders such as autism, schizophrenia, and Tourette syndrome. We generated genetic knockouts for NRXN-1, NRXN-2, and NRXN-3 using CRISPR technology in human stem cells. This approach allowed us to bypass the variability encountered in traditional knockout lines, leading to the creation of polyclonal neurexin knockout cultures. These were then differentiated into induced neurons (iNs) and subjected to detailed analyses of their morphology, synaptic density through immunostaining, and electrophysiological properties via patch clamp recordings. Contrary to our expectations, the deletion of NRXN genes had only limited effects in our observation period, suggesting a potentially limited role of these genes in early development and synapse formation. This suggests the influence of neurexins on neurons may be more subtle and reliant on the biological context than previously understood, highlighting the need for more advanced models to fully grasp their role in brain disorders.

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