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From engineered heart tissue to cardiac organoid
The advent of human pluripotent stem cells (hPSCs) presented a new paradigm to employ hPSC-derived cardiomyocytes (hPSC-CMs) in drug screening and disease modeling. However, hPSC-CMs differentiated in conventional two-dimensional systems are structurally and functionally immature. Moreover, these di...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Ivyspring International Publisher
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965483/ https://www.ncbi.nlm.nih.gov/pubmed/35401829 http://dx.doi.org/10.7150/thno.67661 |
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author | Cho, Jaeyeaon Lee, Hyein Rah, Woongchan Chang, Hyuk Jae Yoon, Young-sup |
author_facet | Cho, Jaeyeaon Lee, Hyein Rah, Woongchan Chang, Hyuk Jae Yoon, Young-sup |
author_sort | Cho, Jaeyeaon |
collection | PubMed |
description | The advent of human pluripotent stem cells (hPSCs) presented a new paradigm to employ hPSC-derived cardiomyocytes (hPSC-CMs) in drug screening and disease modeling. However, hPSC-CMs differentiated in conventional two-dimensional systems are structurally and functionally immature. Moreover, these differentiation systems generate predominantly one type of cell. Since the heart includes not only CMs but other cell types, such monolayer cultures have limitations in simulating the native heart. Accordingly, three-dimensional (3D) cardiac tissues have been developed as a better platform by including various cardiac cell types and extracellular matrices. Two advances were made for 3D cardiac tissue generation. One type is engineered heart tissues (EHTs), which are constructed by 3D cell culture of cardiac cells using an engineering technology. This system provides a convenient real-time analysis of cardiac function, as well as a precise control of the input/output flow and mechanical/electrical stimulation. The other type is cardiac organoids, which are formed through self-organization of differentiating cardiac lineage cells from hPSCs. While mature cardiac organoids are more desirable, at present only primitive forms of organoids are available. In this review, we discuss various models of hEHTs and cardiac organoids emulating the human heart, focusing on their unique features, utility, and limitations. |
format | Online Article Text |
id | pubmed-8965483 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Ivyspring International Publisher |
record_format | MEDLINE/PubMed |
spelling | pubmed-89654832022-04-07 From engineered heart tissue to cardiac organoid Cho, Jaeyeaon Lee, Hyein Rah, Woongchan Chang, Hyuk Jae Yoon, Young-sup Theranostics Review The advent of human pluripotent stem cells (hPSCs) presented a new paradigm to employ hPSC-derived cardiomyocytes (hPSC-CMs) in drug screening and disease modeling. However, hPSC-CMs differentiated in conventional two-dimensional systems are structurally and functionally immature. Moreover, these differentiation systems generate predominantly one type of cell. Since the heart includes not only CMs but other cell types, such monolayer cultures have limitations in simulating the native heart. Accordingly, three-dimensional (3D) cardiac tissues have been developed as a better platform by including various cardiac cell types and extracellular matrices. Two advances were made for 3D cardiac tissue generation. One type is engineered heart tissues (EHTs), which are constructed by 3D cell culture of cardiac cells using an engineering technology. This system provides a convenient real-time analysis of cardiac function, as well as a precise control of the input/output flow and mechanical/electrical stimulation. The other type is cardiac organoids, which are formed through self-organization of differentiating cardiac lineage cells from hPSCs. While mature cardiac organoids are more desirable, at present only primitive forms of organoids are available. In this review, we discuss various models of hEHTs and cardiac organoids emulating the human heart, focusing on their unique features, utility, and limitations. Ivyspring International Publisher 2022-03-14 /pmc/articles/PMC8965483/ /pubmed/35401829 http://dx.doi.org/10.7150/thno.67661 Text en © The author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/). See http://ivyspring.com/terms for full terms and conditions. |
spellingShingle | Review Cho, Jaeyeaon Lee, Hyein Rah, Woongchan Chang, Hyuk Jae Yoon, Young-sup From engineered heart tissue to cardiac organoid |
title | From engineered heart tissue to cardiac organoid |
title_full | From engineered heart tissue to cardiac organoid |
title_fullStr | From engineered heart tissue to cardiac organoid |
title_full_unstemmed | From engineered heart tissue to cardiac organoid |
title_short | From engineered heart tissue to cardiac organoid |
title_sort | from engineered heart tissue to cardiac organoid |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8965483/ https://www.ncbi.nlm.nih.gov/pubmed/35401829 http://dx.doi.org/10.7150/thno.67661 |
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