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Microphysiological stem cell models of the human heart
Models of heart disease and drug responses are increasingly based on human pluripotent stem cells (hPSCs) since their ability to capture human heart (dys-)function is often better than animal models. Simple monolayer cultures of hPSC-derived cardiomyocytes, however, have shortcomings. Some of these...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062349/ https://www.ncbi.nlm.nih.gov/pubmed/35514437 http://dx.doi.org/10.1016/j.mtbio.2022.100259 |
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author | Arslan, Ulgu Moruzzi, Alessia Nowacka, Joanna Mummery, Christine L. Eckardt, Dominik Loskill, Peter Orlova, Valeria V. |
author_facet | Arslan, Ulgu Moruzzi, Alessia Nowacka, Joanna Mummery, Christine L. Eckardt, Dominik Loskill, Peter Orlova, Valeria V. |
author_sort | Arslan, Ulgu |
collection | PubMed |
description | Models of heart disease and drug responses are increasingly based on human pluripotent stem cells (hPSCs) since their ability to capture human heart (dys-)function is often better than animal models. Simple monolayer cultures of hPSC-derived cardiomyocytes, however, have shortcomings. Some of these can be overcome using more complex, multi cell-type models in 3D. Here we review modalities that address this, describe efforts to tailor readouts and sensors for monitoring tissue- and cell physiology (exogenously and in situ) and discuss perspectives for implementation in industry and academia. |
format | Online Article Text |
id | pubmed-9062349 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90623492022-05-04 Microphysiological stem cell models of the human heart Arslan, Ulgu Moruzzi, Alessia Nowacka, Joanna Mummery, Christine L. Eckardt, Dominik Loskill, Peter Orlova, Valeria V. Mater Today Bio Review Article Models of heart disease and drug responses are increasingly based on human pluripotent stem cells (hPSCs) since their ability to capture human heart (dys-)function is often better than animal models. Simple monolayer cultures of hPSC-derived cardiomyocytes, however, have shortcomings. Some of these can be overcome using more complex, multi cell-type models in 3D. Here we review modalities that address this, describe efforts to tailor readouts and sensors for monitoring tissue- and cell physiology (exogenously and in situ) and discuss perspectives for implementation in industry and academia. Elsevier 2022-04-14 /pmc/articles/PMC9062349/ /pubmed/35514437 http://dx.doi.org/10.1016/j.mtbio.2022.100259 Text en © 2022 The Authors https://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 | Review Article Arslan, Ulgu Moruzzi, Alessia Nowacka, Joanna Mummery, Christine L. Eckardt, Dominik Loskill, Peter Orlova, Valeria V. Microphysiological stem cell models of the human heart |
title | Microphysiological stem cell models of the human heart |
title_full | Microphysiological stem cell models of the human heart |
title_fullStr | Microphysiological stem cell models of the human heart |
title_full_unstemmed | Microphysiological stem cell models of the human heart |
title_short | Microphysiological stem cell models of the human heart |
title_sort | microphysiological stem cell models of the human heart |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062349/ https://www.ncbi.nlm.nih.gov/pubmed/35514437 http://dx.doi.org/10.1016/j.mtbio.2022.100259 |
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