Ensemble recording of electrical activity in neurons derived from P19 embryonal carcinoma cells

Regeneration of the central nervous system (CNS) is one of the most important research themes in neuroscience and neuroengineering. It is essential to replenish the lost neurons and to establish appropriate functional neuronal networks using pluripotent stem cells. Little is known, however, about th...

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Published inElectronics and communications in Japan Vol. 94; no. 4; pp. 9 - 19
Main Authors Takayama, Yuzo, Saito, Atsushi, Moriguchi, Hiroyuki, Kotani, Kiyoshi, Jimbo, Yasuhiko
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.04.2011
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Summary:Regeneration of the central nervous system (CNS) is one of the most important research themes in neuroscience and neuroengineering. It is essential to replenish the lost neurons and to establish appropriate functional neuronal networks using pluripotent stem cells. Little is known, however, about the properties of stem cell‐derived neuronal networks, particularly under the differentiation and development processes. In this work, we cultured P19 embryonal carcinoma cells on microelectrode arrays (MEAs). P19 cells were differentiated into neurons by retinoic acid application and formed densely connected networks. Spontaneous electrical activity was extracellularly recorded through substrate electrodes and analyzed. Synchronized periodic bursts, which were characteristic features in primary cultured CNS neurons, were observed. Pharmacological studies demonstrated that the glutamatergic excitatory synapses and the GABAergic inhibitory synapses were active in these P19‐derived neuronal networks. The results suggested that MEA‐based recording was useful for monitoring differentiation processes of stem cells. P19‐derived neuronal networks had quite similar network properties to those of primary cultured neurons, and thus provide a novel model system to investigate stem cell‐based neuronal regeneration. © 2011 Wiley Periodicals, Inc. Electron Comm Jpn, 94(4): 9–19, 2011; Published online in Wiley Online Library (wileyonlinelibrary.com). DOI 10.1002/ecj.10325
Bibliography:ArticleID:ECJ10325
istex:8C8E4A150580B6AE2A285317638198C4392EE508
Grant-in-Aid for Scientific Research Program of the Japan Society for the Promotion of Science.
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ISSN:1942-9533
1942-9541
1942-9541
DOI:10.1002/ecj.10325