Soni A, Kluetsch D, Hu X, Houtman J, Rund N, Mccloskey A, Mertens J, Schafer ST, Amin H, Toda T (2021)
Publication Type: Journal article
Publication year: 2021
Book Volume: 10
Article Number: 1894
Journal Issue: 8
Neuronal culture was used to investigate neuronal function in physiological and pathological conditions. Despite its inevitability, primary neuronal culture remained a gold standard method that requires laborious preparation, intensive training, and animal resources. To circum-vent the shortfalls of primary neuronal preparations and efficiently give rise to functional neurons, we combine a neural stem cell culture method with a direct cell type-conversion approach. The lucidity of this method enables the efficient preparation of functional neurons from mouse neural progenitor cells on demand. We demonstrate that induced neurons (NPC-iNs) by this method make synaptic connections, elicit neuronal activity-dependent cellular responses, and develop functional neuronal networks. This method will provide a concise platform for functional neuronal assess-ments. This indeed offers a perspective for using these characterized neuronal networks for investigating plasticity mechanisms, drug screening assays, and probing the molecular and biophysical basis of neurodevelopmental and neurodegenerative diseases.
APA:
Soni, A., Kluetsch, D., Hu, X., Houtman, J., Rund, N., Mccloskey, A.,... Toda, T. (2021). Improved method for efficient generation of functional neurons from murine neural progenitor cells. Cells, 10(8). https://dx.doi.org/10.3390/cells10081894
MLA:
Soni, Abhinav, et al. "Improved method for efficient generation of functional neurons from murine neural progenitor cells." Cells 10.8 (2021).
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