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Blinded, multi-centre evaluation of drug-induced changes in contractility using human induced pluripotent stem cell-derived cardiomyocytes

Saleem, Umber; van Meer, Berend J.; Katili, Puspita A.; Yusof, Nurul A N Mohd; Mannhardt, Ingra; Garcia, Ana Krotenberg; Tertoolen, Leon; de Korte, Tessa; Vlaming, Maria L.H.; McGlynn, Karen; Nebel, Jessica; Bahinski, Anthony; Harris, Kate; Rossman, Eric; Xu, Xiaoping; Burton, Francis L.; Smith, Godfrey L.; Clements, Peter; Mummery, Christine L.; Eschenhagen, Thomas; Hansen, Arne; Denning, Chris

Blinded, multi-centre evaluation of drug-induced changes in contractility using human induced pluripotent stem cell-derived cardiomyocytes Thumbnail


Authors

Umber Saleem

Berend J. van Meer

Puspita A. Katili

Nurul A N Mohd Yusof

Ingra Mannhardt

Ana Krotenberg Garcia

Leon Tertoolen

Tessa de Korte

Maria L.H. Vlaming

Karen McGlynn

Jessica Nebel

Anthony Bahinski

Kate Harris

Eric Rossman

Xiaoping Xu

Francis L. Burton

Godfrey L. Smith

Peter Clements

Christine L. Mummery

Thomas Eschenhagen

Arne Hansen

CHRIS DENNING chris.denning@nottingham.ac.uk
Professor of Stem Cell Biology



Abstract

Animal models are 78% accurate in determining whether drugs will alter contractility of the human heart. To evaluate the suitability of human-induced pluripotent stem cell-derived cardiomyocytes (hiPSC-CMs) for predictive safety pharmacology, we quantified changes in contractility, voltage, and/or Ca2+ handling in 2D monolayers or 3D engineered heart tissues (EHTs). Protocols were unified via a drug training set, allowing subsequent blinded multicenter evaluation of drugs with known positive, negative, or neutral inotropic effects. Accuracy ranged from 44% to 85% across the platform-cell configurations, indicating the need to refine test conditions. This was achieved by adopting approaches to reduce signal-to-noise ratio, reduce spontaneous beat rate to ≤ 1 Hz or enable chronic testing, improving accuracy to 85% for monolayers and 93% for EHTs. Contraction amplitude was a good predictor of negative inotropes across all the platform-cell configurations and of positive inotropes in the 3D EHTs. Although contraction- and relaxation-time provided confirmatory readouts forpositive inotropes in 3D EHTs, these parameters typically served as the primary source of predictivity in 2D. The reliance of these “secondary” parameters to inotropy in the 2D systems was not automatically intuitive and may be a quirk of hiPSC-CMs, hence require adaptations in interpreting the data from this model system. Of the platform-cell configurations, responses in EHTs aligned most closely to the free therapeutic plasma concentration. This study adds to the notion that hiPSC-CMs could add value to drug safety evaluation.

Citation

Saleem, U., van Meer, B. J., Katili, P. A., Yusof, N. A. N. M., Mannhardt, I., Garcia, A. K., …Denning, C. (2020). Blinded, multi-centre evaluation of drug-induced changes in contractility using human induced pluripotent stem cell-derived cardiomyocytes. Toxicological Sciences, 176(1), 103–123. https://doi.org/10.1093/toxsci/kfaa058

Journal Article Type Article
Acceptance Date May 1, 2020
Online Publication Date May 18, 2020
Publication Date 2020-07
Deposit Date Jul 20, 2020
Publicly Available Date Jul 21, 2020
Journal Toxicological Sciences
Print ISSN 1096-6080
Electronic ISSN 1096-0929
Publisher Oxford University Press
Peer Reviewed Peer Reviewed
Volume 176
Issue 1
Pages 103–123
DOI https://doi.org/10.1093/toxsci/kfaa058
Keywords Toxicology
Public URL https://nottingham-repository.worktribe.com/output/4606933
Publisher URL https://academic.oup.com/toxsci/article/176/1/103/5839757