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Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium
Cardiomyocytes (CMs) generated from human induced pluripotent stem cells (hiPSCs) are under investigation for their suitability as human models in preclinical drug development. Antiarrhythmic drug development focuses on atrial biology for the treatment of atrial fibrillation. Here we used recent ret...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294072/ https://www.ncbi.nlm.nih.gov/pubmed/30416051 http://dx.doi.org/10.1016/j.stemcr.2018.10.008 |
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author | Lemme, Marta Ulmer, Bärbel M. Lemoine, Marc D. Zech, Antonia T.L. Flenner, Frederik Ravens, Ursula Reichenspurner, Hermann Rol-Garcia, Miriam Smith, Godfrey Hansen, Arne Christ, Torsten Eschenhagen, Thomas |
author_facet | Lemme, Marta Ulmer, Bärbel M. Lemoine, Marc D. Zech, Antonia T.L. Flenner, Frederik Ravens, Ursula Reichenspurner, Hermann Rol-Garcia, Miriam Smith, Godfrey Hansen, Arne Christ, Torsten Eschenhagen, Thomas |
author_sort | Lemme, Marta |
collection | PubMed |
description | Cardiomyocytes (CMs) generated from human induced pluripotent stem cells (hiPSCs) are under investigation for their suitability as human models in preclinical drug development. Antiarrhythmic drug development focuses on atrial biology for the treatment of atrial fibrillation. Here we used recent retinoic acid-based protocols to generate atrial CMs from hiPSCs and establish right atrial engineered heart tissue (RA-EHT) as a 3D model of human atrium. EHT from standard protocol-derived hiPSC-CMs (Ctrl-EHT) and intact human muscle strips served as comparators. RA-EHT exhibited higher mRNA and protein concentrations of atrial-selective markers, faster contraction kinetics, lower force generation, shorter action potential duration, and higher repolarization fraction than Ctrl-EHTs. In addition, RA-EHTs but not Ctrl-EHTs responded to pharmacological manipulation of atrial-selective potassium currents. RA- and Ctrl-EHTs’ behavior reflected differences between human atrial and ventricular muscle preparations. Taken together, RA-EHT is a model of human atrium that may be useful in preclinical drug screening. |
format | Online Article Text |
id | pubmed-6294072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-62940722018-12-21 Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium Lemme, Marta Ulmer, Bärbel M. Lemoine, Marc D. Zech, Antonia T.L. Flenner, Frederik Ravens, Ursula Reichenspurner, Hermann Rol-Garcia, Miriam Smith, Godfrey Hansen, Arne Christ, Torsten Eschenhagen, Thomas Stem Cell Reports Article Cardiomyocytes (CMs) generated from human induced pluripotent stem cells (hiPSCs) are under investigation for their suitability as human models in preclinical drug development. Antiarrhythmic drug development focuses on atrial biology for the treatment of atrial fibrillation. Here we used recent retinoic acid-based protocols to generate atrial CMs from hiPSCs and establish right atrial engineered heart tissue (RA-EHT) as a 3D model of human atrium. EHT from standard protocol-derived hiPSC-CMs (Ctrl-EHT) and intact human muscle strips served as comparators. RA-EHT exhibited higher mRNA and protein concentrations of atrial-selective markers, faster contraction kinetics, lower force generation, shorter action potential duration, and higher repolarization fraction than Ctrl-EHTs. In addition, RA-EHTs but not Ctrl-EHTs responded to pharmacological manipulation of atrial-selective potassium currents. RA- and Ctrl-EHTs’ behavior reflected differences between human atrial and ventricular muscle preparations. Taken together, RA-EHT is a model of human atrium that may be useful in preclinical drug screening. Elsevier 2018-11-08 /pmc/articles/PMC6294072/ /pubmed/30416051 http://dx.doi.org/10.1016/j.stemcr.2018.10.008 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Lemme, Marta Ulmer, Bärbel M. Lemoine, Marc D. Zech, Antonia T.L. Flenner, Frederik Ravens, Ursula Reichenspurner, Hermann Rol-Garcia, Miriam Smith, Godfrey Hansen, Arne Christ, Torsten Eschenhagen, Thomas Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium |
title | Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium |
title_full | Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium |
title_fullStr | Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium |
title_full_unstemmed | Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium |
title_short | Atrial-like Engineered Heart Tissue: An In Vitro Model of the Human Atrium |
title_sort | atrial-like engineered heart tissue: an in vitro model of the human atrium |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6294072/ https://www.ncbi.nlm.nih.gov/pubmed/30416051 http://dx.doi.org/10.1016/j.stemcr.2018.10.008 |
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