诱导多能干细胞
神经元
转录组
神经科学
电生理学
生物
计算生物学
基因
基因表达
胚胎干细胞
遗传学
作者
Xiwei Shan,Ai Zhang,Mitchell G. Rezzonico,Ming‐Chi Tsai,Carlos Sánchez-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
标识
DOI:10.1016/j.crmeth.2024.100858
摘要
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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