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Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative
Organoids hold inestimable therapeutic potential in regenerative medicine and are increasingly serving as an in vitro research platform. Still, their expanding applications are critically restricted by the canonical culture matrix and system. Synthesis of a suitable bioink of bioactivity, biosecurit...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842023/ https://www.ncbi.nlm.nih.gov/pubmed/36684067 http://dx.doi.org/10.1002/btm2.10327 |
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author | Xu, Zi‐Yan Huang, Jin‐Jian Liu, Ye Chen, Can‐Wen Qu, Gui‐Wen Wang, Ge‐Fei Zhao, Yun Wu, Xiu‐Wen Ren, Jian‐An |
author_facet | Xu, Zi‐Yan Huang, Jin‐Jian Liu, Ye Chen, Can‐Wen Qu, Gui‐Wen Wang, Ge‐Fei Zhao, Yun Wu, Xiu‐Wen Ren, Jian‐An |
author_sort | Xu, Zi‐Yan |
collection | PubMed |
description | Organoids hold inestimable therapeutic potential in regenerative medicine and are increasingly serving as an in vitro research platform. Still, their expanding applications are critically restricted by the canonical culture matrix and system. Synthesis of a suitable bioink of bioactivity, biosecurity, tunable stiffness, and printability to replace conventional matrices and fabricate customized culture systems remains challenging. Here, we envisaged a novel bioink formulation based on decellularized extracellular matrix (dECM) from porcine small intestinal submucosa for organoids bioprinting, which provides intestinal stem cells (ISCs) with niche‐specific ECM content and biomimetic microstructure. Intestinal organoids cultured in the fabricated bioink exhibited robust generation as well as a distinct differentiation pattern and transcriptomic signature. This bioink established a new co‐culture system able to study interaction between epithelial homeostasis and submucosal cells and promote organoids maturation after transplantation into the mesentery of immune‐deficient NODSCID‐gamma (NSG) mice. In summary, the development of such photo‐responsive bioink has the potential to replace tumor‐derived Matrigel and facilitate the application of organoids in translational medicine and disease modeling. |
format | Online Article Text |
id | pubmed-9842023 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98420232023-01-19 Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative Xu, Zi‐Yan Huang, Jin‐Jian Liu, Ye Chen, Can‐Wen Qu, Gui‐Wen Wang, Ge‐Fei Zhao, Yun Wu, Xiu‐Wen Ren, Jian‐An Bioeng Transl Med Research Articles Organoids hold inestimable therapeutic potential in regenerative medicine and are increasingly serving as an in vitro research platform. Still, their expanding applications are critically restricted by the canonical culture matrix and system. Synthesis of a suitable bioink of bioactivity, biosecurity, tunable stiffness, and printability to replace conventional matrices and fabricate customized culture systems remains challenging. Here, we envisaged a novel bioink formulation based on decellularized extracellular matrix (dECM) from porcine small intestinal submucosa for organoids bioprinting, which provides intestinal stem cells (ISCs) with niche‐specific ECM content and biomimetic microstructure. Intestinal organoids cultured in the fabricated bioink exhibited robust generation as well as a distinct differentiation pattern and transcriptomic signature. This bioink established a new co‐culture system able to study interaction between epithelial homeostasis and submucosal cells and promote organoids maturation after transplantation into the mesentery of immune‐deficient NODSCID‐gamma (NSG) mice. In summary, the development of such photo‐responsive bioink has the potential to replace tumor‐derived Matrigel and facilitate the application of organoids in translational medicine and disease modeling. John Wiley & Sons, Inc. 2022-04-26 /pmc/articles/PMC9842023/ /pubmed/36684067 http://dx.doi.org/10.1002/btm2.10327 Text en © 2022 The Authors. Bioengineering & Translational Medicine published by Wiley Periodicals LLC on behalf of American Institute of Chemical Engineers. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Xu, Zi‐Yan Huang, Jin‐Jian Liu, Ye Chen, Can‐Wen Qu, Gui‐Wen Wang, Ge‐Fei Zhao, Yun Wu, Xiu‐Wen Ren, Jian‐An Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative |
title | Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative |
title_full | Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative |
title_fullStr | Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative |
title_full_unstemmed | Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative |
title_short | Extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe Matrigel alternative |
title_sort | extracellular matrix bioink boosts stemness and facilitates transplantation of intestinal organoids as a biosafe matrigel alternative |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9842023/ https://www.ncbi.nlm.nih.gov/pubmed/36684067 http://dx.doi.org/10.1002/btm2.10327 |
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