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Tissue-specific micropattern array chips fabricated via decellularized ECM for 3D cell culture
Multicellular three-dimensional (3D) in vitro models, such as cell spheroids and organoids, can significantly improve the viability, histomorphology, genotype stability, function and drug metabolism of cells [1], [2], [3]. In general, several culture methods of 3D models, including the hanging drop,...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652133/ https://www.ncbi.nlm.nih.gov/pubmed/38023305 http://dx.doi.org/10.1016/j.mex.2023.102463 |
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author | Zhu, Xinglong Li, Yi Long, Hulin Liang, Zuoyu He, Yuting Zhou, Yanyan Li, Shun Bao, Ji |
author_facet | Zhu, Xinglong Li, Yi Long, Hulin Liang, Zuoyu He, Yuting Zhou, Yanyan Li, Shun Bao, Ji |
author_sort | Zhu, Xinglong |
collection | PubMed |
description | Multicellular three-dimensional (3D) in vitro models, such as cell spheroids and organoids, can significantly improve the viability, histomorphology, genotype stability, function and drug metabolism of cells [1], [2], [3]. In general, several culture methods of 3D models, including the hanging drop, microwell-mesh and hydrogel encapsulating methods, have difficulty building a standard mode and controlling the size and arrangement of cell spheroids or organoids, which could severely affect the authenticity and repeatability of experimental results [4]. Another key factor in 3D in vitro models is the extracellular matrix (ECM), which can determine cell viability, proliferation, differentiation, function, migration and organization [5]. In this study, micropattern array chips combined with decellularized ECM (dECM) not only provide tissue-specific ECM but also control the size and arrangement of 3D models. • Methods have been established to demonstrate the use of dECM as a bioink to generate dECM-coated micropattern array chips by microcontact printing. • The micropattern can limit cell growth and migration, and cells spontaneously assemble into cell spheroids with uniform size and orderly arrangement. |
format | Online Article Text |
id | pubmed-10652133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-106521332023-10-31 Tissue-specific micropattern array chips fabricated via decellularized ECM for 3D cell culture Zhu, Xinglong Li, Yi Long, Hulin Liang, Zuoyu He, Yuting Zhou, Yanyan Li, Shun Bao, Ji MethodsX Engineering Multicellular three-dimensional (3D) in vitro models, such as cell spheroids and organoids, can significantly improve the viability, histomorphology, genotype stability, function and drug metabolism of cells [1], [2], [3]. In general, several culture methods of 3D models, including the hanging drop, microwell-mesh and hydrogel encapsulating methods, have difficulty building a standard mode and controlling the size and arrangement of cell spheroids or organoids, which could severely affect the authenticity and repeatability of experimental results [4]. Another key factor in 3D in vitro models is the extracellular matrix (ECM), which can determine cell viability, proliferation, differentiation, function, migration and organization [5]. In this study, micropattern array chips combined with decellularized ECM (dECM) not only provide tissue-specific ECM but also control the size and arrangement of 3D models. • Methods have been established to demonstrate the use of dECM as a bioink to generate dECM-coated micropattern array chips by microcontact printing. • The micropattern can limit cell growth and migration, and cells spontaneously assemble into cell spheroids with uniform size and orderly arrangement. Elsevier 2023-10-31 /pmc/articles/PMC10652133/ /pubmed/38023305 http://dx.doi.org/10.1016/j.mex.2023.102463 Text en © 2023 The Authors. Published by Elsevier B.V. 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 | Engineering Zhu, Xinglong Li, Yi Long, Hulin Liang, Zuoyu He, Yuting Zhou, Yanyan Li, Shun Bao, Ji Tissue-specific micropattern array chips fabricated via decellularized ECM for 3D cell culture |
title | Tissue-specific micropattern array chips fabricated via decellularized ECM for 3D cell culture |
title_full | Tissue-specific micropattern array chips fabricated via decellularized ECM for 3D cell culture |
title_fullStr | Tissue-specific micropattern array chips fabricated via decellularized ECM for 3D cell culture |
title_full_unstemmed | Tissue-specific micropattern array chips fabricated via decellularized ECM for 3D cell culture |
title_short | Tissue-specific micropattern array chips fabricated via decellularized ECM for 3D cell culture |
title_sort | tissue-specific micropattern array chips fabricated via decellularized ecm for 3d cell culture |
topic | Engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10652133/ https://www.ncbi.nlm.nih.gov/pubmed/38023305 http://dx.doi.org/10.1016/j.mex.2023.102463 |
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