Literature DB >> 27369811

Points to consider for a validation study of iPS cell-derived cardiomyocytes using a multi-electrode array system.

Yasunari Kanda1, Daiju Yamazaki1, Junko Kurokawa2, Takashi Inutsuka3, Yuko Sekino4.   

Abstract

Human induced pluripotent stem cell-derived cardiomyocytes (iPS-CMs) provide a novel assay system to assess cardiac safety in drug development to overcome a problem of species difference in non-clinical testing during drug development. Using the multi-electrode array (MEA) platform, electrophysiological activities of iPS-CMs can be recorded easily to assess QT prolongation and proarrhythmic potential of drug candidates. Here we have established a standardized protocol to evaluate the possibility of iPS-CMs, and shared the protocol with an international consortium. To obtain reproducible and reliable experimental data from these cells, we determined the optimal experimental conditions, such as cell density, MEA coating, culture conditions, high-pass filter frequency, definition of early afterdepolarization or triggered activity, and calibration compounds. Based on the protocol, our validation study using 60 compounds is in progress. Thus, MEA-based experiments using iPS-CMs would be a standard testing method to evaluate QT prolongation and proarrhythmic potentials.
Copyright © 2016 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Cardiac safety pharmacology; Human iPS cells; JiCSA; Multi-electrode array; Proarrhythmia; Standardization

Mesh:

Year:  2016        PMID: 27369811     DOI: 10.1016/j.vascn.2016.06.007

Source DB:  PubMed          Journal:  J Pharmacol Toxicol Methods        ISSN: 1056-8719            Impact factor:   1.950


  7 in total

1.  Cross - site comparison of excitation-contraction coupling using impedance and field potential recordings in hiPSC cardiomyocytes.

Authors:  Corina T Bot; Krisztina Juhasz; Fabian Haeusermann; Liudmila Polonchuk; Martin Traebert; Sonja Stoelzle-Feix
Journal:  J Pharmacol Toxicol Methods       Date:  2018-06-22       Impact factor: 1.950

2.  Turning Potential Into Action: Using Pluripotent Stem Cells to Understand Heart Development and Function in Health and Disease.

Authors:  Hananeh Fonoudi; Alexis Bosman
Journal:  Stem Cells Transl Med       Date:  2017-03-24       Impact factor: 6.940

Review 3.  hiPSC-Derived Cardiac Tissue for Disease Modeling and Drug Discovery.

Authors:  Junjun Li; Ying Hua; Shigeru Miyagawa; Jingbo Zhang; Lingjun Li; Li Liu; Yoshiki Sawa
Journal:  Int J Mol Sci       Date:  2020-11-24       Impact factor: 5.923

Review 4.  The Challenges of Predicting Drug-Induced QTc Prolongation in Humans.

Authors:  Jean-Pierre Valentin; Peter Hoffmann; Catherine Ortemann-Renon; John Koerner; Jennifer Pierson; Gary Gintant; James Willard; Christine Garnett; Matthew Skinner; Hugo M Vargas; Todd Wisialowski; Michael K Pugsley
Journal:  Toxicol Sci       Date:  2022-04-26       Impact factor: 4.109

Review 5.  Human Engineered Heart Tissue Models for Disease Modeling and Drug Discovery.

Authors:  Hidenori Tani; Shugo Tohyama
Journal:  Front Cell Dev Biol       Date:  2022-03-31

6.  Involvement of kallikrein-PAR2-proinflammatory pathway in severe trastuzumab-induced cardiotoxicity.

Authors:  Ritsuko Sasaki; Nagomi Kurebayashi; Hidetaka Eguchi; Yoshiya Horimoto; Takahiro Shiga; Sakiko Miyazaki; Taku Kashiyama; Wado Akamatsu; Mitsue Saito
Journal:  Cancer Sci       Date:  2022-08-19       Impact factor: 6.518

Review 7.  hiPSCs Derived Cardiac Cells for Drug and Toxicity Screening and Disease Modeling: What Micro- Electrode-Array Analyses Can Tell Us.

Authors:  Sophie Kussauer; Robert David; Heiko Lemcke
Journal:  Cells       Date:  2019-10-28       Impact factor: 6.600

  7 in total

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