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Human Engineered Heart Tissue Models for Disease Modeling and Drug Discovery
The emergence of human induced pluripotent stem cells (hiPSCs) and efficient differentiation of hiPSC-derived cardiomyocytes (hiPSC-CMs) induced from diseased donors have the potential to recapitulate the molecular and functional features of the human heart. Although the immaturity of hiPSC-CMs, inc...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9008275/ https://www.ncbi.nlm.nih.gov/pubmed/35433691 http://dx.doi.org/10.3389/fcell.2022.855763 |
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author | Tani, Hidenori Tohyama, Shugo |
author_facet | Tani, Hidenori Tohyama, Shugo |
author_sort | Tani, Hidenori |
collection | PubMed |
description | The emergence of human induced pluripotent stem cells (hiPSCs) and efficient differentiation of hiPSC-derived cardiomyocytes (hiPSC-CMs) induced from diseased donors have the potential to recapitulate the molecular and functional features of the human heart. Although the immaturity of hiPSC-CMs, including the structure, gene expression, conduct, ion channel density, and Ca(2+) kinetics, is a major challenge, various attempts to promote maturation have been effective. Three-dimensional cardiac models using hiPSC-CMs have achieved these functional and morphological maturations, and disease models using patient-specific hiPSC-CMs have furthered our understanding of the underlying mechanisms and effective therapies for diseases. Aside from the mechanisms of diseases and drug responses, hiPSC-CMs also have the potential to evaluate the safety and efficacy of drugs in a human context before a candidate drug enters the market and many phases of clinical trials. In fact, novel drug testing paradigms have suggested that these cells can be used to better predict the proarrhythmic risk of candidate drugs. In this review, we overview the current strategies of human engineered heart tissue models with a focus on major cardiac diseases and discuss perspectives and future directions for the real application of hiPSC-CMs and human engineered heart tissue for disease modeling, drug development, clinical trials, and cardiotoxicity tests. |
format | Online Article Text |
id | pubmed-9008275 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-90082752022-04-15 Human Engineered Heart Tissue Models for Disease Modeling and Drug Discovery Tani, Hidenori Tohyama, Shugo Front Cell Dev Biol Cell and Developmental Biology The emergence of human induced pluripotent stem cells (hiPSCs) and efficient differentiation of hiPSC-derived cardiomyocytes (hiPSC-CMs) induced from diseased donors have the potential to recapitulate the molecular and functional features of the human heart. Although the immaturity of hiPSC-CMs, including the structure, gene expression, conduct, ion channel density, and Ca(2+) kinetics, is a major challenge, various attempts to promote maturation have been effective. Three-dimensional cardiac models using hiPSC-CMs have achieved these functional and morphological maturations, and disease models using patient-specific hiPSC-CMs have furthered our understanding of the underlying mechanisms and effective therapies for diseases. Aside from the mechanisms of diseases and drug responses, hiPSC-CMs also have the potential to evaluate the safety and efficacy of drugs in a human context before a candidate drug enters the market and many phases of clinical trials. In fact, novel drug testing paradigms have suggested that these cells can be used to better predict the proarrhythmic risk of candidate drugs. In this review, we overview the current strategies of human engineered heart tissue models with a focus on major cardiac diseases and discuss perspectives and future directions for the real application of hiPSC-CMs and human engineered heart tissue for disease modeling, drug development, clinical trials, and cardiotoxicity tests. Frontiers Media S.A. 2022-03-31 /pmc/articles/PMC9008275/ /pubmed/35433691 http://dx.doi.org/10.3389/fcell.2022.855763 Text en Copyright © 2022 Tani and Tohyama. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Tani, Hidenori Tohyama, Shugo Human Engineered Heart Tissue Models for Disease Modeling and Drug Discovery |
title | Human Engineered Heart Tissue Models for Disease Modeling and Drug Discovery |
title_full | Human Engineered Heart Tissue Models for Disease Modeling and Drug Discovery |
title_fullStr | Human Engineered Heart Tissue Models for Disease Modeling and Drug Discovery |
title_full_unstemmed | Human Engineered Heart Tissue Models for Disease Modeling and Drug Discovery |
title_short | Human Engineered Heart Tissue Models for Disease Modeling and Drug Discovery |
title_sort | human engineered heart tissue models for disease modeling and drug discovery |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9008275/ https://www.ncbi.nlm.nih.gov/pubmed/35433691 http://dx.doi.org/10.3389/fcell.2022.855763 |
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