Development and characterization of a scaffold-free 3D spheroid model of iPSC-derived human cardiomyocytes

Beauchamp, Philippe; Ullrich, Nina; Jens, Kelm; Moritz, Wolfgang; Agarkova, Irina; Anson, Blake; Suter, Thomas; Zuppinger, Christian (2015). Development and characterization of a scaffold-free 3D spheroid model of iPSC-derived human cardiomyocytes. Tissue engineering Part C Methods, 21(8), pp. 852-861. Mary Ann Liebert 10.1089/ten.tec.2014.0376

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Purpose: Cardiomyocytes are terminally differentiated cells in the adult heart and ischemia and cardiotoxic compounds can lead to cell death and irreversible decline of cardiac function. As testing platforms, isolated organs and primary cells from rodents have been the standard in research and toxicology, but there is a need for better models that more faithfully recapitulate native human biology. Hence, a new in vitro model comprising the advantages of 3D cell culture and the availability of induced pluripotent stem cells (iPSC) from human origin was developed and characterized.
Methods: Human cardiomyocytes (CMs) derived from induced pluripotent stem cells (iPSCs) were studied in standard 2D culture and as cardiac microtissues (MTs) formed in hanging drops. 2D cultures were examined using immunofluorescence microscopy and Western blotting while the cardiac MTs were subjected to immunofluorescence, contractility, and pharmacological investigations.
Results: iPSC-derived CMs in 2D culture showed well-formed myofibrils, cell-cell contacts positive for connexin-43, and other typical cardiac proteins. The cells reacted to pro-hypertrophic growth factors with a substantial increase in myofibrils and sarcomeric proteins. In hanging drop cultures, iPSC-derived cardiomyocytes formed spheroidal MTs within 4 days showing a homogeneous tissue structure with well-developed myofibrils extending throughout the whole spheroid without a necrotic core. MTs showed spontaneous contractions for more than 4 weeks that were recorded by optical motion tracking, sensitive to temperature, and responsive to electrical pacing. Contractile pharmacology was tested with several agents known to modulate cardiac rate and viability. Calcium-transients underlay the contractile activity and were also responsive to electrical stimulation, caffeine-induced Ca2+-release, extracellular calcium levels.
Conclusions: 3D culture using iPSC-derived human cardiomyocytes provides an organoid human-based cellular platform that is free of necrosis and recapitulates vital cardiac functionality, thereby providing new and promising relevant model for the evaluation and development of new therapies and detection of cardiotoxicity.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > DBMR Forschung Mu35 > Forschungsgruppe Kardiologie
04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR) > DBMR Forschung Mu35 > Forschungsgruppe Kardiologie

04 Faculty of Medicine > Pre-clinic Human Medicine > Institute of Physiology

UniBE Contributor:

Beauchamp, Philippe Jacques Abel, Ullrich, Nina Daniela, Suter, Thomas, Zuppinger, Christian

Subjects:

600 Technology > 610 Medicine & health

ISSN:

1937-3384

Publisher:

Mary Ann Liebert

Language:

English

Submitter:

Christian Zuppinger

Date Deposited:

30 Sep 2015 10:43

Last Modified:

02 Mar 2023 23:26

Publisher DOI:

10.1089/ten.tec.2014.0376

PubMed ID:

25654582

Uncontrolled Keywords:

3D culture, induced pluripotent stem cells, cardiomyocytes, cardiotoxicity, toxicology, heart

BORIS DOI:

10.7892/boris.72049

URI:

https://boris.unibe.ch/id/eprint/72049

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