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Middle-out methods for spatiotemporal tissue engineering of organoids
Organoids recapitulate many aspects of the complex three-dimensional (3D) organization found within native tissues and even display tissue and organ-level functionality. Traditional approaches to organoid culture have largely employed a top-down tissue engineering strategy, whereby cells are encapsu...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010248/ https://www.ncbi.nlm.nih.gov/pubmed/37168734 http://dx.doi.org/10.1038/s44222-023-00039-3 |
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author | Blatchley, Michael R. Anseth, Kristi S. |
author_facet | Blatchley, Michael R. Anseth, Kristi S. |
author_sort | Blatchley, Michael R. |
collection | PubMed |
description | Organoids recapitulate many aspects of the complex three-dimensional (3D) organization found within native tissues and even display tissue and organ-level functionality. Traditional approaches to organoid culture have largely employed a top-down tissue engineering strategy, whereby cells are encapsulated in a 3D matrix, such as Matrigel, alongside well-defined biochemical cues that direct morphogenesis. However, the lack of spatiotemporal control over niche properties renders cellular processes largely stochastic. Therefore, bottom-up tissue engineering approaches have evolved to address some of these limitations and focus on strategies to assemble tissue building blocks with defined multi-scale spatial organization. However, bottom-up design reduces the capacity for self-organization that underpins organoid morphogenesis. Here, we introduce an emerging framework, which we term middle-out strategies, that relies on existing design principles and combines top-down design of defined synthetic matrices that support proliferation and self-organization with bottom-up modular engineered intervention to limit the degrees of freedom in the dynamic process of organoid morphogenesis. We posit that this strategy will provide key advances to guide the growth of organoids with precise geometries, structures and function, thereby facilitating an unprecedented level of biomimicry to accelerate the utility of organoids to more translationally relevant applications. |
format | Online Article Text |
id | pubmed-10010248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100102482023-03-14 Middle-out methods for spatiotemporal tissue engineering of organoids Blatchley, Michael R. Anseth, Kristi S. Nat Rev Bioeng Review Article Organoids recapitulate many aspects of the complex three-dimensional (3D) organization found within native tissues and even display tissue and organ-level functionality. Traditional approaches to organoid culture have largely employed a top-down tissue engineering strategy, whereby cells are encapsulated in a 3D matrix, such as Matrigel, alongside well-defined biochemical cues that direct morphogenesis. However, the lack of spatiotemporal control over niche properties renders cellular processes largely stochastic. Therefore, bottom-up tissue engineering approaches have evolved to address some of these limitations and focus on strategies to assemble tissue building blocks with defined multi-scale spatial organization. However, bottom-up design reduces the capacity for self-organization that underpins organoid morphogenesis. Here, we introduce an emerging framework, which we term middle-out strategies, that relies on existing design principles and combines top-down design of defined synthetic matrices that support proliferation and self-organization with bottom-up modular engineered intervention to limit the degrees of freedom in the dynamic process of organoid morphogenesis. We posit that this strategy will provide key advances to guide the growth of organoids with precise geometries, structures and function, thereby facilitating an unprecedented level of biomimicry to accelerate the utility of organoids to more translationally relevant applications. Nature Publishing Group UK 2023-03-13 2023 /pmc/articles/PMC10010248/ /pubmed/37168734 http://dx.doi.org/10.1038/s44222-023-00039-3 Text en © Springer Nature Limited 2023, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Article Blatchley, Michael R. Anseth, Kristi S. Middle-out methods for spatiotemporal tissue engineering of organoids |
title | Middle-out methods for spatiotemporal tissue engineering of organoids |
title_full | Middle-out methods for spatiotemporal tissue engineering of organoids |
title_fullStr | Middle-out methods for spatiotemporal tissue engineering of organoids |
title_full_unstemmed | Middle-out methods for spatiotemporal tissue engineering of organoids |
title_short | Middle-out methods for spatiotemporal tissue engineering of organoids |
title_sort | middle-out methods for spatiotemporal tissue engineering of organoids |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10010248/ https://www.ncbi.nlm.nih.gov/pubmed/37168734 http://dx.doi.org/10.1038/s44222-023-00039-3 |
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