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3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels
Cellular models are needed to study human development and disease in vitro, and to screen drugs for toxicity and efficacy. Current approaches are limited in the engineering of functional tissue models with requisite cell densities and heterogeneity to appropriately model cell and tissue behaviors. H...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854667/ https://www.ncbi.nlm.nih.gov/pubmed/33531489 http://dx.doi.org/10.1038/s41467-021-21029-2 |
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author | Daly, Andrew C. Davidson, Matthew D. Burdick, Jason A. |
author_facet | Daly, Andrew C. Davidson, Matthew D. Burdick, Jason A. |
author_sort | Daly, Andrew C. |
collection | PubMed |
description | Cellular models are needed to study human development and disease in vitro, and to screen drugs for toxicity and efficacy. Current approaches are limited in the engineering of functional tissue models with requisite cell densities and heterogeneity to appropriately model cell and tissue behaviors. Here, we develop a bioprinting approach to transfer spheroids into self-healing support hydrogels at high resolution, which enables their patterning and fusion into high-cell density microtissues of prescribed spatial organization. As an example application, we bioprint induced pluripotent stem cell-derived cardiac microtissue models with spatially controlled cardiomyocyte and fibroblast cell ratios to replicate the structural and functional features of scarred cardiac tissue that arise following myocardial infarction, including reduced contractility and irregular electrical activity. The bioprinted in vitro model is combined with functional readouts to probe how various pro-regenerative microRNA treatment regimes influence tissue regeneration and recovery of function as a result of cardiomyocyte proliferation. This method is useful for a range of biomedical applications, including the development of precision models to mimic diseases and the screening of drugs, particularly where high cell densities and heterogeneity are important. |
format | Online Article Text |
id | pubmed-7854667 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-78546672021-02-11 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels Daly, Andrew C. Davidson, Matthew D. Burdick, Jason A. Nat Commun Article Cellular models are needed to study human development and disease in vitro, and to screen drugs for toxicity and efficacy. Current approaches are limited in the engineering of functional tissue models with requisite cell densities and heterogeneity to appropriately model cell and tissue behaviors. Here, we develop a bioprinting approach to transfer spheroids into self-healing support hydrogels at high resolution, which enables their patterning and fusion into high-cell density microtissues of prescribed spatial organization. As an example application, we bioprint induced pluripotent stem cell-derived cardiac microtissue models with spatially controlled cardiomyocyte and fibroblast cell ratios to replicate the structural and functional features of scarred cardiac tissue that arise following myocardial infarction, including reduced contractility and irregular electrical activity. The bioprinted in vitro model is combined with functional readouts to probe how various pro-regenerative microRNA treatment regimes influence tissue regeneration and recovery of function as a result of cardiomyocyte proliferation. This method is useful for a range of biomedical applications, including the development of precision models to mimic diseases and the screening of drugs, particularly where high cell densities and heterogeneity are important. Nature Publishing Group UK 2021-02-02 /pmc/articles/PMC7854667/ /pubmed/33531489 http://dx.doi.org/10.1038/s41467-021-21029-2 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Daly, Andrew C. Davidson, Matthew D. Burdick, Jason A. 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels |
title | 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels |
title_full | 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels |
title_fullStr | 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels |
title_full_unstemmed | 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels |
title_short | 3D bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels |
title_sort | 3d bioprinting of high cell-density heterogeneous tissue models through spheroid fusion within self-healing hydrogels |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7854667/ https://www.ncbi.nlm.nih.gov/pubmed/33531489 http://dx.doi.org/10.1038/s41467-021-21029-2 |
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