Publication

Fully defined NGN2 neuron protocol reveals diverse signatures of neuronal maturation

September 16, 2024
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Custom Analysis
Functional Phenotyping
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MaxTwo 6-Well Plate
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Neuronal Cell Cultures
Xiwei Shan, Ai Zhang, Mitchell G. Rezzonico, Ming-Chi Tsai, Carlos Sanchez-Priego, Yingjie Zhang, Michelle B. Chen, Meena Choi, José Miguel Andrade López, Lilian Phu, Amber L. Cramer, Qiao Zhang, Jillian M. Pattison, Christopher M. Rose, Casper C. Hoogenraad, Claire G. Jeong
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Abstract

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NGN2-driven induced pluripotent stem cell (iPSC)-to-neuron conversion is a popular method for human neurological disease modeling. In this study, we present a standardized approach for generating neurons utilizing clonal, targeted-engineered iPSC lines with defined reagents. We demonstrate consistent production of excitatory neurons at scale and long-term maintenance for at least 150 days. Temporal omics, electrophysiological, and morphological profiling indicate continued maturation to postnatal-like neurons. Quantitative characterizations through transcriptomic, imaging, and functional assays reveal coordinated actions of multiple pathways that drive neuronal maturation. We also show the expression of disease-related genes in these neurons to demonstrate the relevance of our protocol for modeling neurological disorders. Finally, we demonstrate efficient generation of NGN2-integrated iPSC lines. These workflows, profiling data, and functional characterizations enable the development of reproducible human in vitro models of neurological disorders.