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Polyisocyanide Hydrogels as a Tunable Platform for Mammary Gland Organoid Formation
In the last decade, organoid technology has developed as a primary research tool in basic biological and clinical research. The reliance on poorly defined animal‐derived extracellular matrix, however, severely limits its application in regenerative and translational medicine. Here, a well‐defined, s...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509700/ https://www.ncbi.nlm.nih.gov/pubmed/32999851 http://dx.doi.org/10.1002/advs.202001797 |
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author | Zhang, Ying Tang, Chunling Span, Paul N. Rowan, Alan E. Aalders, Tilly W. Schalken, Jack A. Adema, Gosse J. Kouwer, Paul H. J. Zegers, Mirjam M. P. Ansems, Marleen |
author_facet | Zhang, Ying Tang, Chunling Span, Paul N. Rowan, Alan E. Aalders, Tilly W. Schalken, Jack A. Adema, Gosse J. Kouwer, Paul H. J. Zegers, Mirjam M. P. Ansems, Marleen |
author_sort | Zhang, Ying |
collection | PubMed |
description | In the last decade, organoid technology has developed as a primary research tool in basic biological and clinical research. The reliance on poorly defined animal‐derived extracellular matrix, however, severely limits its application in regenerative and translational medicine. Here, a well‐defined, synthetic biomimetic matrix based on polyisocyanide (PIC) hydrogels that support efficient and reproducible formation of mammary gland organoids (MGOs) in vitro is presented. Only decorated with the adhesive peptide RGD for cell binding, PIC hydrogels allow MGO formation from mammary fragments or from purified single mammary epithelial cells. The cystic organoids maintain their capacity to branch for over two months, which is a fundamental and complex feature during mammary gland development. It is found that small variations in the 3D matrix give rise to large changes in the MGO: the ratio of the main cell types in the MGO is controlled by the cell–gel interactions via the cell binding peptide density, whereas gel stiffness controls colony formation efficiency, which is indicative of the progenitor density. Simple hydrogel modifications will allow for future introduction and customization of new biophysical and biochemical parameters, making the PIC platform an ideal matrix for in depth studies into organ development and for application in disease models. |
format | Online Article Text |
id | pubmed-7509700 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75097002020-09-29 Polyisocyanide Hydrogels as a Tunable Platform for Mammary Gland Organoid Formation Zhang, Ying Tang, Chunling Span, Paul N. Rowan, Alan E. Aalders, Tilly W. Schalken, Jack A. Adema, Gosse J. Kouwer, Paul H. J. Zegers, Mirjam M. P. Ansems, Marleen Adv Sci (Weinh) Full Papers In the last decade, organoid technology has developed as a primary research tool in basic biological and clinical research. The reliance on poorly defined animal‐derived extracellular matrix, however, severely limits its application in regenerative and translational medicine. Here, a well‐defined, synthetic biomimetic matrix based on polyisocyanide (PIC) hydrogels that support efficient and reproducible formation of mammary gland organoids (MGOs) in vitro is presented. Only decorated with the adhesive peptide RGD for cell binding, PIC hydrogels allow MGO formation from mammary fragments or from purified single mammary epithelial cells. The cystic organoids maintain their capacity to branch for over two months, which is a fundamental and complex feature during mammary gland development. It is found that small variations in the 3D matrix give rise to large changes in the MGO: the ratio of the main cell types in the MGO is controlled by the cell–gel interactions via the cell binding peptide density, whereas gel stiffness controls colony formation efficiency, which is indicative of the progenitor density. Simple hydrogel modifications will allow for future introduction and customization of new biophysical and biochemical parameters, making the PIC platform an ideal matrix for in depth studies into organ development and for application in disease models. John Wiley and Sons Inc. 2020-07-26 /pmc/articles/PMC7509700/ /pubmed/32999851 http://dx.doi.org/10.1002/advs.202001797 Text en © 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Full Papers Zhang, Ying Tang, Chunling Span, Paul N. Rowan, Alan E. Aalders, Tilly W. Schalken, Jack A. Adema, Gosse J. Kouwer, Paul H. J. Zegers, Mirjam M. P. Ansems, Marleen Polyisocyanide Hydrogels as a Tunable Platform for Mammary Gland Organoid Formation |
title | Polyisocyanide Hydrogels as a Tunable Platform for Mammary Gland Organoid Formation |
title_full | Polyisocyanide Hydrogels as a Tunable Platform for Mammary Gland Organoid Formation |
title_fullStr | Polyisocyanide Hydrogels as a Tunable Platform for Mammary Gland Organoid Formation |
title_full_unstemmed | Polyisocyanide Hydrogels as a Tunable Platform for Mammary Gland Organoid Formation |
title_short | Polyisocyanide Hydrogels as a Tunable Platform for Mammary Gland Organoid Formation |
title_sort | polyisocyanide hydrogels as a tunable platform for mammary gland organoid formation |
topic | Full Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509700/ https://www.ncbi.nlm.nih.gov/pubmed/32999851 http://dx.doi.org/10.1002/advs.202001797 |
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