Human neuronal networks on micro-electrode arrays are a highly robust tool to study disease-specific genotype-phenotype correlations in vitro.
Human neuronal networks on micro-electrode arrays are a highly robust tool to study disease-specific genotype-phenotype correlations in vitro.
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DOI:
10.1016/j.stemcr.2021.07.001
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发表时间:
2021-09-14
影响因子:
5.9
通讯作者:
Frega M
中科院分区:
文献类型:
--
作者:
Mossink B;Verboven AHA;van Hugte EJH;Klein Gunnewiek TM;Parodi G;Linda K;Schoenmaker C;Kleefstra T;Kozicz T;van Bokhoven H;Schubert D;Nadif Kasri N;Frega M
Micro-electrode arrays (MEAs) are increasingly used to characterize neuronal network activity of human induced pluripotent stem cell (hiPSC)-derived neurons. Despite their gain in popularity, MEA recordings from hiPSC-derived neuronal networks are not always used to their full potential in respect to experimental design, execution, and data analysis. Therefore, we benchmarked the robustness of MEA-derived neuronal activity patterns from ten healthy individual control lines, and uncover comparable network phenotypes. To achieve standardization, we provide recommendations on experimental design and analysis. With such standardization, MEAs can be used as a reliable platform to distinguish (disease-specific) network phenotypes. In conclusion, we show that MEAs are a powerful and robust tool to uncover functional neuronal network phenotypes from hiPSC-derived neuronal networks, and provide an important resource to advance the hiPSC field toward the use of MEAs for disease phenotyping and drug discovery. MEAs are a robust tool to model neuronal network functioning Neuronal networks from different healthy donors show comparable network activity MEAs are able to distinguish disease-specific neuronal network phenotypes We provide recommendations to standardize neuronal network recordings on MEA In this article, Mossink and colleagues demonstrate that micro-electrode arrays (MEAs) are a highly robust tool to uncover genotype/phenotype interactions in hiPSC-derived excitatory neuronal networks, and provide an important resource for the design, execution, and analysis of hiPSC-derived neuronal networks studies on MEA.
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DOI:
10.1083/jcb.85.3.890
发表时间:
1980-06
期刊:
The Journal of cell biology
影响因子:
--
作者:
McCarthy KD;de Vellis J
通讯作者:
de Vellis J
影响因子:
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DOI:
10.1038/nrn.2016.46
发表时间:
2016-07
期刊:
Nature reviews. Neuroscience
影响因子:
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Mertens J;Marchetto MC;Bardy C;Gage FH
通讯作者:
Gage FH
影响因子:
1.2
作者:
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通讯作者:
Narkilahti, Susanna
DOI:
10.1073/pnas.0910012107
发表时间:
2010-03-02
影响因子:
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作者:
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Zhang, Su-Chun