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Kartogenin‐Conjugated Double‐Network Hydrogel Combined with Stem Cell Transplantation and Tracing for Cartilage Repair

The effectiveness of existing tissue‐engineering cartilage (TEC) is known to be hampered by weak integration of biocompatibility, biodegradation, mechanical strength, and microenvironment supplies. The strategy of hydrogel‐based TEC holds considerable promise in circumventing these problems. Herein,...

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Autores principales: Chen, You‐Rong, Yan, Xin, Yuan, Fu‐Zhen, Lin, Lin, Wang, Shao‐Jie, Ye, Jing, Zhang, Ji‐Ying, Yang, Meng, Wu, De‐Cheng, Wang, Xing, Yu, Jia‐Kuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762312/
https://www.ncbi.nlm.nih.gov/pubmed/36253092
http://dx.doi.org/10.1002/advs.202105571
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author Chen, You‐Rong
Yan, Xin
Yuan, Fu‐Zhen
Lin, Lin
Wang, Shao‐Jie
Ye, Jing
Zhang, Ji‐Ying
Yang, Meng
Wu, De‐Cheng
Wang, Xing
Yu, Jia‐Kuo
author_facet Chen, You‐Rong
Yan, Xin
Yuan, Fu‐Zhen
Lin, Lin
Wang, Shao‐Jie
Ye, Jing
Zhang, Ji‐Ying
Yang, Meng
Wu, De‐Cheng
Wang, Xing
Yu, Jia‐Kuo
author_sort Chen, You‐Rong
collection PubMed
description The effectiveness of existing tissue‐engineering cartilage (TEC) is known to be hampered by weak integration of biocompatibility, biodegradation, mechanical strength, and microenvironment supplies. The strategy of hydrogel‐based TEC holds considerable promise in circumventing these problems. Herein, a non‐toxic, biodegradable, and mechanically optimized double‐network (DN) hydrogel consisting of polyethylene glycol (PEG) and kartogenin (KGN)‐conjugated chitosan (CHI) is constructed using a simple soaking strategy. This PEG‐CHI‐KGN DN hydrogel possesses favorable architectures, suitable mechanics, remarkable cellular affinity, and sustained KGN release, which can facilitate the cartilage‐specific genes expression and extracellular matrix secretion of peripheral blood‐derived mesenchymal stem cells (PB‐MSCs). Notably, after tracing the transplanted cells by detecting the rabbit sex‐determining region Y‐linked gene sequence, the allogeneic PB‐MSCs are found to survive for even 3 months in the regenerated cartilage. Here, the long‐term release of KGN is able to efficiently and persistently activate multiple genes and signaling pathways to promote the chondrogenesis, chondrocyte differentiation, and survival of PB‐MSCs. Thus, the regenerated tissues exhibit well‐matched histomorphology and biomechanical performance such as native cartilage. Consequently, it is believed this innovative work can expand the choice for developing the next generation of orthopedic implants in the loadbearing region of a living body.
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spelling pubmed-97623122022-12-20 Kartogenin‐Conjugated Double‐Network Hydrogel Combined with Stem Cell Transplantation and Tracing for Cartilage Repair Chen, You‐Rong Yan, Xin Yuan, Fu‐Zhen Lin, Lin Wang, Shao‐Jie Ye, Jing Zhang, Ji‐Ying Yang, Meng Wu, De‐Cheng Wang, Xing Yu, Jia‐Kuo Adv Sci (Weinh) Research Articles The effectiveness of existing tissue‐engineering cartilage (TEC) is known to be hampered by weak integration of biocompatibility, biodegradation, mechanical strength, and microenvironment supplies. The strategy of hydrogel‐based TEC holds considerable promise in circumventing these problems. Herein, a non‐toxic, biodegradable, and mechanically optimized double‐network (DN) hydrogel consisting of polyethylene glycol (PEG) and kartogenin (KGN)‐conjugated chitosan (CHI) is constructed using a simple soaking strategy. This PEG‐CHI‐KGN DN hydrogel possesses favorable architectures, suitable mechanics, remarkable cellular affinity, and sustained KGN release, which can facilitate the cartilage‐specific genes expression and extracellular matrix secretion of peripheral blood‐derived mesenchymal stem cells (PB‐MSCs). Notably, after tracing the transplanted cells by detecting the rabbit sex‐determining region Y‐linked gene sequence, the allogeneic PB‐MSCs are found to survive for even 3 months in the regenerated cartilage. Here, the long‐term release of KGN is able to efficiently and persistently activate multiple genes and signaling pathways to promote the chondrogenesis, chondrocyte differentiation, and survival of PB‐MSCs. Thus, the regenerated tissues exhibit well‐matched histomorphology and biomechanical performance such as native cartilage. Consequently, it is believed this innovative work can expand the choice for developing the next generation of orthopedic implants in the loadbearing region of a living body. John Wiley and Sons Inc. 2022-10-17 /pmc/articles/PMC9762312/ /pubmed/36253092 http://dx.doi.org/10.1002/advs.202105571 Text en © 2022 The Authors. Advanced Science published by Wiley‐VCH GmbH 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
Chen, You‐Rong
Yan, Xin
Yuan, Fu‐Zhen
Lin, Lin
Wang, Shao‐Jie
Ye, Jing
Zhang, Ji‐Ying
Yang, Meng
Wu, De‐Cheng
Wang, Xing
Yu, Jia‐Kuo
Kartogenin‐Conjugated Double‐Network Hydrogel Combined with Stem Cell Transplantation and Tracing for Cartilage Repair
title Kartogenin‐Conjugated Double‐Network Hydrogel Combined with Stem Cell Transplantation and Tracing for Cartilage Repair
title_full Kartogenin‐Conjugated Double‐Network Hydrogel Combined with Stem Cell Transplantation and Tracing for Cartilage Repair
title_fullStr Kartogenin‐Conjugated Double‐Network Hydrogel Combined with Stem Cell Transplantation and Tracing for Cartilage Repair
title_full_unstemmed Kartogenin‐Conjugated Double‐Network Hydrogel Combined with Stem Cell Transplantation and Tracing for Cartilage Repair
title_short Kartogenin‐Conjugated Double‐Network Hydrogel Combined with Stem Cell Transplantation and Tracing for Cartilage Repair
title_sort kartogenin‐conjugated double‐network hydrogel combined with stem cell transplantation and tracing for cartilage repair
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9762312/
https://www.ncbi.nlm.nih.gov/pubmed/36253092
http://dx.doi.org/10.1002/advs.202105571
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