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Silk fibroin/cartilage extracellular matrix scaffolds with sequential delivery of TGF-β3 for chondrogenic differentiation of adipose-derived stem cells

A 3-D scaffold that simulates the microenvironment in vivo for regenerating cartilage is ideal. In this study, we combined silk fibroin and decellularized cartilage extracellular matrix by temperature gradient-guided thermal-induced phase separation to produce composite scaffolds (S/D). Resulting sc...

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Autores principales: Yang, Qiang, Teng, Bin-Hong, Wang, Li-Na, Li, Kun, Xu, Chen, Ma, Xin-Long, Zhang, Yang, Kong, De-Ling, Wang, Lian-Yong, Zhao, Yan-Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600265/
https://www.ncbi.nlm.nih.gov/pubmed/28932116
http://dx.doi.org/10.2147/IJN.S141888
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author Yang, Qiang
Teng, Bin-Hong
Wang, Li-Na
Li, Kun
Xu, Chen
Ma, Xin-Long
Zhang, Yang
Kong, De-Ling
Wang, Lian-Yong
Zhao, Yan-Hong
author_facet Yang, Qiang
Teng, Bin-Hong
Wang, Li-Na
Li, Kun
Xu, Chen
Ma, Xin-Long
Zhang, Yang
Kong, De-Ling
Wang, Lian-Yong
Zhao, Yan-Hong
author_sort Yang, Qiang
collection PubMed
description A 3-D scaffold that simulates the microenvironment in vivo for regenerating cartilage is ideal. In this study, we combined silk fibroin and decellularized cartilage extracellular matrix by temperature gradient-guided thermal-induced phase separation to produce composite scaffolds (S/D). Resulting scaffolds had remarkable mechanical properties and biomimeticstructure, for a suitable substrate for attachment and proliferation of adipose-derived stem cells (ADSCs). Moreover, transforming growth factor β3 (TGF-β3) loaded on scaffolds showed a controlled release profile and enhanced the chondrogenic differentiation of ADSCs during the 28-day culture. The S/D scaffold itself can provide a sustained release system without the introduction of other controlled release media, which has potential for commercial and clinical applications. The results of toluidine blue, Safranin O, and immunohistochemical staining and analysis of collagen II expression showed maintenance of a chondrogenic phenotype in all scaffolds after 28-day culture. The most obvious phenomenon was with the addition of TGF-β3. S/D composite scaffolds with sequential delivery of TGF-β3 may mimic the regenerative microenvironment to enhance the chondrogenic differentiation of ADSCs in vitro.
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spelling pubmed-56002652017-09-20 Silk fibroin/cartilage extracellular matrix scaffolds with sequential delivery of TGF-β3 for chondrogenic differentiation of adipose-derived stem cells Yang, Qiang Teng, Bin-Hong Wang, Li-Na Li, Kun Xu, Chen Ma, Xin-Long Zhang, Yang Kong, De-Ling Wang, Lian-Yong Zhao, Yan-Hong Int J Nanomedicine Original Research A 3-D scaffold that simulates the microenvironment in vivo for regenerating cartilage is ideal. In this study, we combined silk fibroin and decellularized cartilage extracellular matrix by temperature gradient-guided thermal-induced phase separation to produce composite scaffolds (S/D). Resulting scaffolds had remarkable mechanical properties and biomimeticstructure, for a suitable substrate for attachment and proliferation of adipose-derived stem cells (ADSCs). Moreover, transforming growth factor β3 (TGF-β3) loaded on scaffolds showed a controlled release profile and enhanced the chondrogenic differentiation of ADSCs during the 28-day culture. The S/D scaffold itself can provide a sustained release system without the introduction of other controlled release media, which has potential for commercial and clinical applications. The results of toluidine blue, Safranin O, and immunohistochemical staining and analysis of collagen II expression showed maintenance of a chondrogenic phenotype in all scaffolds after 28-day culture. The most obvious phenomenon was with the addition of TGF-β3. S/D composite scaffolds with sequential delivery of TGF-β3 may mimic the regenerative microenvironment to enhance the chondrogenic differentiation of ADSCs in vitro. Dove Medical Press 2017-09-11 /pmc/articles/PMC5600265/ /pubmed/28932116 http://dx.doi.org/10.2147/IJN.S141888 Text en © 2017 Yang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Yang, Qiang
Teng, Bin-Hong
Wang, Li-Na
Li, Kun
Xu, Chen
Ma, Xin-Long
Zhang, Yang
Kong, De-Ling
Wang, Lian-Yong
Zhao, Yan-Hong
Silk fibroin/cartilage extracellular matrix scaffolds with sequential delivery of TGF-β3 for chondrogenic differentiation of adipose-derived stem cells
title Silk fibroin/cartilage extracellular matrix scaffolds with sequential delivery of TGF-β3 for chondrogenic differentiation of adipose-derived stem cells
title_full Silk fibroin/cartilage extracellular matrix scaffolds with sequential delivery of TGF-β3 for chondrogenic differentiation of adipose-derived stem cells
title_fullStr Silk fibroin/cartilage extracellular matrix scaffolds with sequential delivery of TGF-β3 for chondrogenic differentiation of adipose-derived stem cells
title_full_unstemmed Silk fibroin/cartilage extracellular matrix scaffolds with sequential delivery of TGF-β3 for chondrogenic differentiation of adipose-derived stem cells
title_short Silk fibroin/cartilage extracellular matrix scaffolds with sequential delivery of TGF-β3 for chondrogenic differentiation of adipose-derived stem cells
title_sort silk fibroin/cartilage extracellular matrix scaffolds with sequential delivery of tgf-β3 for chondrogenic differentiation of adipose-derived stem cells
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5600265/
https://www.ncbi.nlm.nih.gov/pubmed/28932116
http://dx.doi.org/10.2147/IJN.S141888
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