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The effect of collagen hydrogels on chondrocyte behaviors through restricting the contraction of cell/hydrogel constructs
Collagen is a promising material for tissue engineering, but the poor mechanical properties of collagen hydrogels, which tend to cause contraction under the action of cellular activity, make its application challengeable. In this study, the amino group of type I collagen (Col I) was modified with me...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245754/ https://www.ncbi.nlm.nih.gov/pubmed/34221449 http://dx.doi.org/10.1093/rb/rbab030 |
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author | Dong, Longpeng Liu, Qingli Gao, Yongli Jia, Hengxing Dai, Wenling Guo, Likun Fan, Hongsong Fan, Yujiang Zhang, Xingdong |
author_facet | Dong, Longpeng Liu, Qingli Gao, Yongli Jia, Hengxing Dai, Wenling Guo, Likun Fan, Hongsong Fan, Yujiang Zhang, Xingdong |
author_sort | Dong, Longpeng |
collection | PubMed |
description | Collagen is a promising material for tissue engineering, but the poor mechanical properties of collagen hydrogels, which tend to cause contraction under the action of cellular activity, make its application challengeable. In this study, the amino group of type I collagen (Col I) was modified with methacrylic anhydride (MA) and the photo-crosslinkable methacrylate anhydride modified type I collagen (CM) with three different degrees of substitution (DS) was prepared. The physical properties of CM and Col I hydrogels were tested, including micromorphology, mechanical properties and degradation properties. The results showed that the storage modulus and degradation rate of hydrogels could be adjusted by changing the DS of CM. In vitro, chondrocytes were seeded into these four groups of hydrogels and subjected to fluorescein diacetate/propidium iodide (FDA/PI) staining, cell counting kit-8 (CCK-8) test, histological staining and cartilage-related gene expression analysis. In vivo, these hydrogels encapsulating chondrocytes were implanted subcutaneously into nude mice, then histological staining and sulfated glycosaminoglycan (sGAG)/DNA assays were performed. The results demonstrated that contraction of hydrogels affected behaviors of chondrocytes, and CM hydrogels with suitable DS could resist contraction of hydrogels and promote the secretion of cartilage-specific matrix in vitro and in vivo. |
format | Online Article Text |
id | pubmed-8245754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-82457542021-07-02 The effect of collagen hydrogels on chondrocyte behaviors through restricting the contraction of cell/hydrogel constructs Dong, Longpeng Liu, Qingli Gao, Yongli Jia, Hengxing Dai, Wenling Guo, Likun Fan, Hongsong Fan, Yujiang Zhang, Xingdong Regen Biomater Research Article Collagen is a promising material for tissue engineering, but the poor mechanical properties of collagen hydrogels, which tend to cause contraction under the action of cellular activity, make its application challengeable. In this study, the amino group of type I collagen (Col I) was modified with methacrylic anhydride (MA) and the photo-crosslinkable methacrylate anhydride modified type I collagen (CM) with three different degrees of substitution (DS) was prepared. The physical properties of CM and Col I hydrogels were tested, including micromorphology, mechanical properties and degradation properties. The results showed that the storage modulus and degradation rate of hydrogels could be adjusted by changing the DS of CM. In vitro, chondrocytes were seeded into these four groups of hydrogels and subjected to fluorescein diacetate/propidium iodide (FDA/PI) staining, cell counting kit-8 (CCK-8) test, histological staining and cartilage-related gene expression analysis. In vivo, these hydrogels encapsulating chondrocytes were implanted subcutaneously into nude mice, then histological staining and sulfated glycosaminoglycan (sGAG)/DNA assays were performed. The results demonstrated that contraction of hydrogels affected behaviors of chondrocytes, and CM hydrogels with suitable DS could resist contraction of hydrogels and promote the secretion of cartilage-specific matrix in vitro and in vivo. Oxford University Press 2021-07-01 /pmc/articles/PMC8245754/ /pubmed/34221449 http://dx.doi.org/10.1093/rb/rbab030 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Dong, Longpeng Liu, Qingli Gao, Yongli Jia, Hengxing Dai, Wenling Guo, Likun Fan, Hongsong Fan, Yujiang Zhang, Xingdong The effect of collagen hydrogels on chondrocyte behaviors through restricting the contraction of cell/hydrogel constructs |
title | The effect of collagen hydrogels on chondrocyte behaviors through restricting the contraction of cell/hydrogel constructs |
title_full | The effect of collagen hydrogels on chondrocyte behaviors through restricting the contraction of cell/hydrogel constructs |
title_fullStr | The effect of collagen hydrogels on chondrocyte behaviors through restricting the contraction of cell/hydrogel constructs |
title_full_unstemmed | The effect of collagen hydrogels on chondrocyte behaviors through restricting the contraction of cell/hydrogel constructs |
title_short | The effect of collagen hydrogels on chondrocyte behaviors through restricting the contraction of cell/hydrogel constructs |
title_sort | effect of collagen hydrogels on chondrocyte behaviors through restricting the contraction of cell/hydrogel constructs |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8245754/ https://www.ncbi.nlm.nih.gov/pubmed/34221449 http://dx.doi.org/10.1093/rb/rbab030 |
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