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Pharmacological Responses in Cultured Human iPSC-Derived Cortical Neurons Using Multi-Electrode Array
Poster Title: Pharmacological Responses in Cultured Human iPSC-Derived Cortical Neurons Using Multi-Electrode Array
Submitted on 05 Apr 2016
Author(s): Aoi Odawara (1,2), Hiroki Katoh (1), Naoki Matsuda (1), Karolina Szczesna (3), Yichen Shi (3), Ryan Arant (4), Hideyasu Jiko (4), Ikuro Suzuki (1)
Affiliations: (1) Department of Electronics and Intelligent Systems, Tohoku Institute of Technology, Sendai, Miyagi, Japan; (2) Japan Society for the Promotion of Science, Tokyo, Japan; (3) Axol Bioscience Ltd., Cambridge, United Kingdom; (4) Alpha MED Scientific Inc., Osaka, Japan
This poster was presented at Stem Cells in Drug Discovery 2016
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Poster Information
Abstract: Human induced pluripotent stem cell (hiPSC)-derived neurons may be used effectively for drug discovery and cell-based therapy. However, this is limited by the immaturity of cultured hiPSC-derived neurons and the lack of established functional evaluation methods. We used a multi-electrode array (MEA) system to investigate the effects of co-culturing astrocytes with hiPSC-derived cortical neurons on long-term culture, spontaneous firing activity, and drug responsiveness. The co-culture facilitated long-term culture of hiPSC-derived neurons over 400 days. Long-term spontaneous firing activity was also observed. After >3 months in culture, we observed synchronous burst firing activity due to synapse transmission within neuronal networks. Compared with rat neurons, hiPSC-derived neurons required a longer time to mature functionally. In drug response studies, addition of the synapse antagonist bicuculline, CNQX and AP5, and the agonist, L-glutamate, a kainic acid, induced significant changes in the firing rate and synchronised burst firing patterns. Furthermore, administration of pentylentetrazole (PTZ) induced epileptiform activity. Anti-epilepsy drugs, phenytoin and sodium valproate, reduced epileptiform activity. These results suggest that long-term electrophysiological measurements in hiPSC-derived neurons using an MEA system may be beneficial for clarifying the functions of human neuronal circuits and drug screening applications.Summary: The functional network of human induced pluripotent stem cell (hiPSC)-derived neurons is a potentially powerful in vitro model for evaluating disease mechanisms and drug responses. However, the culture time required for the full functional maturation of individual neurons and networks is uncertain. We investigated the development of spontaneous electrophysiological activity and pharmacological responses for over 1 year in culture using multi-electrode arrays (MEAs). References: (1) Shi Y, Kirwan P, Livesey FJ. Nature Protocols 2012Report abuse »
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