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Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons
Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons
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Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons
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Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons
Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons

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Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons
Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons
Journal Article

Polyethyleneimine facilitates the growth and electrophysiological characterization of iPSC-derived motor neurons

2024
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Overview
Induced pluripotent stem cell (iPSC) technology, in combination with electrophysiological characterization via multielectrode array (MEA), has facilitated the utilization of iPSC-derived motor neurons (iPSC-MNs) as highly valuable models for underpinning pathogenic mechanisms and developing novel therapeutic interventions for motor neuron diseases (MNDs). However, the challenge of MN adherence to the MEA plate and the heterogeneity presented in iPSC-derived cultures raise concerns about the reproducibility of the findings obtained from these cellular models. We discovered that one novel factor modulating the electrophysiological activity of iPSC-MNs is the extracellular matrix (ECM) used in the coating to support in vitro growth, differentiation and maturation of iPSC-MNs. The current study showed that two coating conditions, namely, Poly-L-ornithine/Matrigel (POM) and Polyethyleneimine (PEI) strongly promoted attachment of iPSC-MNs on MEA culture dishes compared to three other coating conditions, and both facilitated the maturation of iPSC-MNs as characterized by the detection of extensive electrophysiological activities from the MEA plates. POM coating accelerated the maturation of the iPSC-MNs for up to 5 weeks, which suits modeling of neurodevelopmental disorders. However, the application of PEI resulted in more even distribution of the MNs on the culture dish and reduced variability of electrophysiological signals from the iPSC-MNs in 7-week cultures, which permitted the detection of enhanced excitability in iPSC-MNs from patients with amyotrophic lateral sclerosis (ALS). This study provides a comprehensive comparison of five coating conditions and offers POM and PEI as favorable coatings for in vitro modeling of neurodevelopmental and neurodegenerative disorders, respectively.