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A Multiwell Cardiac µGMEA Platform for Action Potential Recordings from Human iPSC-Derived Cardiomyocyte Constructs.
Edwards, Stacie L; Zlochiver, Viviana; Conrad, Donald B; Vaidyanathan, Ravi; Valiquette, Andrew M; Joshi-Mukherjee, Rosy.
Afiliação
  • Edwards SL; Aurora Research Institute, Aurora Health Care, 960 N 12th Avenue, Milwaukee, WI 53233, USA.
  • Zlochiver V; Aurora Research Institute, Aurora Health Care, 960 N 12th Avenue, Milwaukee, WI 53233, USA.
  • Conrad DB; Aurora Research Institute, Aurora Health Care, 960 N 12th Avenue, Milwaukee, WI 53233, USA.
  • Vaidyanathan R; Cellular and Molecular Arrhythmia Research Program, Department of Medicine, Division of Cardiovascular Medicine, University of Wisconsin, Madison, WI 53705, USA.
  • Valiquette AM; School of Medicine, Creighton University, Omaha, NE 68178, USA.
  • Joshi-Mukherjee R; Aurora Research Institute, Aurora Health Care, 960 N 12th Avenue, Milwaukee, WI 53233, USA; Department of Medicine-Cardiovascular, School of Medicine, Johns Hopkins University; Baltimore, MD 21205, USA. Electronic address: rosy.joshi-mukherjee@aurora.org.
Stem Cell Reports ; 11(2): 522-536, 2018 08 14.
Article em En | MEDLINE | ID: mdl-30033088
Multielectrode array (MEA) technology has been extensively used for field potential recordings from excitable cells. However, its application for action potential (AP) measurements has not been harnessed. Here, we report a novel platform for high-resolution intracellular AP recordings from induced pluripotent stem cell-cardiomyocyte constructs derived from human cardiac fibroblasts. To gain intracellular access, micro-gold MEAs were used to electroporate multiple constructs simultaneously. High-throughput AP measurements were obtained from 41 multicellular constructs. Repeated electroporations of the same cells did not affect the signal stability. Our model has the capability to distinguish subtle differences in AP morphology to characterize the network profile. Furthermore, we confirm the reliability of the system by recapitulating known drug-induced physiological and arrhythmogenic responses. Overall, the model provides a unique cardio-electronic interface for non-invasive measurements of AP dynamics for drug screening and disease modeling. This technology opens the door for identifying novel cardio-factors to enhance electrophysiological maturation.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Potenciais de Ação / Técnicas Eletrofisiológicas Cardíacas / Miócitos Cardíacos / Células-Tronco Pluripotentes Induzidas Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Potenciais de Ação / Técnicas Eletrofisiológicas Cardíacas / Miócitos Cardíacos / Células-Tronco Pluripotentes Induzidas Idioma: En Ano de publicação: 2018 Tipo de documento: Article