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Effect of different aged cartilage ECM on chondrogenesis of BMSCs in vitro and in vivo
Extracellular matrix (ECM)-based biomaterials are promising candidates in cartilage tissue engineering by simulating the native microenvironment to regulate the chondrogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) without exogenous growth factors. The biological properties of E...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7748452/ https://www.ncbi.nlm.nih.gov/pubmed/33365144 http://dx.doi.org/10.1093/rb/rbaa028 |
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author | Wang, Xiuyu Lu, Yan Wang, Wan Wang, Qiguang Liang, Jie Fan, Yujiang Zhang, Xingdong |
author_facet | Wang, Xiuyu Lu, Yan Wang, Wan Wang, Qiguang Liang, Jie Fan, Yujiang Zhang, Xingdong |
author_sort | Wang, Xiuyu |
collection | PubMed |
description | Extracellular matrix (ECM)-based biomaterials are promising candidates in cartilage tissue engineering by simulating the native microenvironment to regulate the chondrogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) without exogenous growth factors. The biological properties of ECM scaffolds are primarily depended on the original source, which would directly influence the chondrogenic effects of the ECM materials. Despite the expanding investigations on ECM scaffolds in recent years, the selection of optimized ECM materials in cartilage regeneration was less reported. In this study, we harvested and compared the articular cartilage ECM from newborn, juvenile and adult rabbits. The results demonstrated the significant differences in the mechanical strength, sulphated glycosaminoglycan and collagen contents of the different aged ECM, before and after decellularization. Consequently, different compositional and mechanical properties were shown in the three ECM-based collagen hydrogels, which exerted age-dependent chondrogenic inducibility. In general, both in vitro and in vivo results suggested that the newborn ECM promoted the most chondrogenesis of BMSCs but led to severe matrix calcification. In contrast, BMSCs synthesized the lowest amount of cartilaginous matrix with minimal calcification with adult ECM. The juvenile ECM achieved the best overall results in promoting chondrogenesis of BMSCs and preventing matrix calcification. Together, this study provides important information to our current knowledge in the design of future ECM-based biomaterials towards a successful repair of articular cartilage. |
format | Online Article Text |
id | pubmed-7748452 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-77484522020-12-22 Effect of different aged cartilage ECM on chondrogenesis of BMSCs in vitro and in vivo Wang, Xiuyu Lu, Yan Wang, Wan Wang, Qiguang Liang, Jie Fan, Yujiang Zhang, Xingdong Regen Biomater Research Articles Extracellular matrix (ECM)-based biomaterials are promising candidates in cartilage tissue engineering by simulating the native microenvironment to regulate the chondrogenic differentiation of bone marrow mesenchymal stem cells (BMSCs) without exogenous growth factors. The biological properties of ECM scaffolds are primarily depended on the original source, which would directly influence the chondrogenic effects of the ECM materials. Despite the expanding investigations on ECM scaffolds in recent years, the selection of optimized ECM materials in cartilage regeneration was less reported. In this study, we harvested and compared the articular cartilage ECM from newborn, juvenile and adult rabbits. The results demonstrated the significant differences in the mechanical strength, sulphated glycosaminoglycan and collagen contents of the different aged ECM, before and after decellularization. Consequently, different compositional and mechanical properties were shown in the three ECM-based collagen hydrogels, which exerted age-dependent chondrogenic inducibility. In general, both in vitro and in vivo results suggested that the newborn ECM promoted the most chondrogenesis of BMSCs but led to severe matrix calcification. In contrast, BMSCs synthesized the lowest amount of cartilaginous matrix with minimal calcification with adult ECM. The juvenile ECM achieved the best overall results in promoting chondrogenesis of BMSCs and preventing matrix calcification. Together, this study provides important information to our current knowledge in the design of future ECM-based biomaterials towards a successful repair of articular cartilage. Oxford University Press 2020-08-04 /pmc/articles/PMC7748452/ /pubmed/33365144 http://dx.doi.org/10.1093/rb/rbaa028 Text en © The Author(s) 2020. Published by Oxford University Press. http://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/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Wang, Xiuyu Lu, Yan Wang, Wan Wang, Qiguang Liang, Jie Fan, Yujiang Zhang, Xingdong Effect of different aged cartilage ECM on chondrogenesis of BMSCs in vitro and in vivo |
title | Effect of different aged cartilage ECM on chondrogenesis of BMSCs in vitro and in vivo |
title_full | Effect of different aged cartilage ECM on chondrogenesis of BMSCs in vitro and in vivo |
title_fullStr | Effect of different aged cartilage ECM on chondrogenesis of BMSCs in vitro and in vivo |
title_full_unstemmed | Effect of different aged cartilage ECM on chondrogenesis of BMSCs in vitro and in vivo |
title_short | Effect of different aged cartilage ECM on chondrogenesis of BMSCs in vitro and in vivo |
title_sort | effect of different aged cartilage ecm on chondrogenesis of bmscs in vitro and in vivo |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7748452/ https://www.ncbi.nlm.nih.gov/pubmed/33365144 http://dx.doi.org/10.1093/rb/rbaa028 |
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