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Multicellular Bioprinting of Biomimetic Inks for Tendon‐to‐Bone Regeneration

Tendon‐to‐bone interface has a hierarchical structure and gradient component that are conducive to distributing the stresses to achieve movement. Conventional biomaterials lack the capacity to induce synchronous repair of multiple tissues, resulting in the failure of the interface repair. Biomimetic...

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Autores principales: Du, Lin, Qin, Chen, Zhang, Hongjian, Han, Fei, Xue, Jianmin, Wang, Yufeng, Wu, Jinfu, Xiao, Yin, Huan, Zhiguang, Wu, Chengtie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375072/
https://www.ncbi.nlm.nih.gov/pubmed/37119499
http://dx.doi.org/10.1002/advs.202301309
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author Du, Lin
Qin, Chen
Zhang, Hongjian
Han, Fei
Xue, Jianmin
Wang, Yufeng
Wu, Jinfu
Xiao, Yin
Huan, Zhiguang
Wu, Chengtie
author_facet Du, Lin
Qin, Chen
Zhang, Hongjian
Han, Fei
Xue, Jianmin
Wang, Yufeng
Wu, Jinfu
Xiao, Yin
Huan, Zhiguang
Wu, Chengtie
author_sort Du, Lin
collection PubMed
description Tendon‐to‐bone interface has a hierarchical structure and gradient component that are conducive to distributing the stresses to achieve movement. Conventional biomaterials lack the capacity to induce synchronous repair of multiple tissues, resulting in the failure of the interface repair. Biomimetic strategies have attracted enormous attention in the field of complex structure regeneration because they can meet the different physiological requirements of multiple tissues. Herein, a biomimetic ink mimicking tendon/bone tissues is developed by combining tendon/bone‐related cells and Mo‐containing silicate (MS) bioceramics. Subsequently, biomimetic multicellular scaffolds are fabricated to achieve the simulation of the hierarchical structure and cellular composition of tendon‐to‐bone interfaces by the spatial distribution of the biomimetic inks via 3D bioprinting, which is of great significance for inducing the regeneration of complex structures in the interface region. In addition, attributed to the desirable ionic microenvironment created by MS bioceramics, the biomimetic scaffolds possess the dual function of inducing tendon/bone‐related cells tenogenic and osteogenic differentiation in vitro, and promote the integrated regeneration of tendon‐to‐bone interfaces in vivo. The study offers a feasible strategy to construct biomimetic multicellular scaffolds with bifunction for inducing multi‐lineage tissue regeneration, especially for regenerating soft‐to‐hard tissue interfaces.
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spelling pubmed-103750722023-07-29 Multicellular Bioprinting of Biomimetic Inks for Tendon‐to‐Bone Regeneration Du, Lin Qin, Chen Zhang, Hongjian Han, Fei Xue, Jianmin Wang, Yufeng Wu, Jinfu Xiao, Yin Huan, Zhiguang Wu, Chengtie Adv Sci (Weinh) Research Articles Tendon‐to‐bone interface has a hierarchical structure and gradient component that are conducive to distributing the stresses to achieve movement. Conventional biomaterials lack the capacity to induce synchronous repair of multiple tissues, resulting in the failure of the interface repair. Biomimetic strategies have attracted enormous attention in the field of complex structure regeneration because they can meet the different physiological requirements of multiple tissues. Herein, a biomimetic ink mimicking tendon/bone tissues is developed by combining tendon/bone‐related cells and Mo‐containing silicate (MS) bioceramics. Subsequently, biomimetic multicellular scaffolds are fabricated to achieve the simulation of the hierarchical structure and cellular composition of tendon‐to‐bone interfaces by the spatial distribution of the biomimetic inks via 3D bioprinting, which is of great significance for inducing the regeneration of complex structures in the interface region. In addition, attributed to the desirable ionic microenvironment created by MS bioceramics, the biomimetic scaffolds possess the dual function of inducing tendon/bone‐related cells tenogenic and osteogenic differentiation in vitro, and promote the integrated regeneration of tendon‐to‐bone interfaces in vivo. The study offers a feasible strategy to construct biomimetic multicellular scaffolds with bifunction for inducing multi‐lineage tissue regeneration, especially for regenerating soft‐to‐hard tissue interfaces. John Wiley and Sons Inc. 2023-04-29 /pmc/articles/PMC10375072/ /pubmed/37119499 http://dx.doi.org/10.1002/advs.202301309 Text en © 2023 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
Du, Lin
Qin, Chen
Zhang, Hongjian
Han, Fei
Xue, Jianmin
Wang, Yufeng
Wu, Jinfu
Xiao, Yin
Huan, Zhiguang
Wu, Chengtie
Multicellular Bioprinting of Biomimetic Inks for Tendon‐to‐Bone Regeneration
title Multicellular Bioprinting of Biomimetic Inks for Tendon‐to‐Bone Regeneration
title_full Multicellular Bioprinting of Biomimetic Inks for Tendon‐to‐Bone Regeneration
title_fullStr Multicellular Bioprinting of Biomimetic Inks for Tendon‐to‐Bone Regeneration
title_full_unstemmed Multicellular Bioprinting of Biomimetic Inks for Tendon‐to‐Bone Regeneration
title_short Multicellular Bioprinting of Biomimetic Inks for Tendon‐to‐Bone Regeneration
title_sort multicellular bioprinting of biomimetic inks for tendon‐to‐bone regeneration
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10375072/
https://www.ncbi.nlm.nih.gov/pubmed/37119499
http://dx.doi.org/10.1002/advs.202301309
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