Fully defined NGN2 neuron protocol reveals diverse signatures of neuronal maturation

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.

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Publication Details

Journal
Cell Reports Methods
Published
2024-09-01
DOI
https://doi.org/10.1016/j.crmeth.2024.100858
Citations
26
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
6.08

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article

Fully defined NGN2 neuron protocol reveals diverse signatures of neuronal maturation

Meena Choi, Carlos Sánchez-Priego, Mitchell G. Rezzonico, Ming‐Chi Tsai et al.
26 citations
Cell Reports Methods
CRISPR and Genetic Engineering
6.08
article

Fully defined NGN2 neuron protocol reveals diverse signatures of neuronal maturation

Meena Choi, Carlos Sánchez-Priego, Mitchell G. Rezzonico, Ming‐Chi Tsai, Casper C. Hoogenraad, Christopher M. Rose, Yingjie Zhang, Michelle B. Chen, Xiwei Shan, Jillian M. Pattison, Qiao Zhang, Ai Zhang, Amber Cramer, José Miguel Andrade López, Lilian Phu, Claire G. Jeong
article en
26 citations

Abstract

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.

Cell Reports MethodsVol. 4(9)
Gene Therapy Laboratory (FR), Advanced Pharma (US), Genomic Health (United States) (US)
Genentech
Zero hunger
Openalex Percentile: Top 3%
CRISPR and Genetic Engineering
6.08
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