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3D Biomimetic Calcified Cartilaginous Callus that Induces Type H Vessels Formation and Osteoclastogenesis

The formation of a calcified cartilaginous callus (CACC) is crucial during bone repair. CACC can stimulate the invasion of type H vessels into the callus to couple angiogenesis and osteogenesis, induce osteoclastogenesis to resorb the calcified matrix, and promote osteoclast secretion of factors to...

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Autores principales: Qiu, Minglong, Li, Changwei, Cai, Zhengwei, Li, Cuidi, Yang, Kai, Tulufu, Nijiati, Chen, Bo, Cheng, Liang, Zhuang, Chengyu, Liu, Zhihong, Qi, Jin, Cui, Wenguo, Deng, Lianfu
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/PMC10238192/
https://www.ncbi.nlm.nih.gov/pubmed/36999832
http://dx.doi.org/10.1002/advs.202207089
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author Qiu, Minglong
Li, Changwei
Cai, Zhengwei
Li, Cuidi
Yang, Kai
Tulufu, Nijiati
Chen, Bo
Cheng, Liang
Zhuang, Chengyu
Liu, Zhihong
Qi, Jin
Cui, Wenguo
Deng, Lianfu
author_facet Qiu, Minglong
Li, Changwei
Cai, Zhengwei
Li, Cuidi
Yang, Kai
Tulufu, Nijiati
Chen, Bo
Cheng, Liang
Zhuang, Chengyu
Liu, Zhihong
Qi, Jin
Cui, Wenguo
Deng, Lianfu
author_sort Qiu, Minglong
collection PubMed
description The formation of a calcified cartilaginous callus (CACC) is crucial during bone repair. CACC can stimulate the invasion of type H vessels into the callus to couple angiogenesis and osteogenesis, induce osteoclastogenesis to resorb the calcified matrix, and promote osteoclast secretion of factors to enhance osteogenesis, ultimately achieving the replacement of cartilage with bone. In this study, a porous polycaprolactone/hydroxyapatite‐iminodiacetic acid‐deferoxamine (PCL/HA‐SF‐DFO) 3D biomimetic CACC is developed using 3D printing. The porous structure can mimic the pores formed by the matrix metalloproteinase degradation of the cartilaginous matrix, HA‐containing PCL can mimic the calcified cartilaginous matrix, and SF anchors DFO onto HA for the slow release of DFO. The in vitro results show that the scaffold significantly enhances angiogenesis, promotes osteoclastogenesis and resorption by osteoclasts, and enhances the osteogenic differentiation of bone marrow stromal stem cells by promoting collagen triple helix repeat‐containing 1 expression by osteoclasts. The in vivo results show that the scaffold significantly promotes type H vessels formation and the expression of coupling factors to promote osteogenesis, ultimately enhancing the regeneration of large‐segment bone defects in rats and preventing dislodging of the internal fixation screw. In conclusion, the scaffold inspired by biological bone repair processes effectively promotes bone regeneration.
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spelling pubmed-102381922023-06-04 3D Biomimetic Calcified Cartilaginous Callus that Induces Type H Vessels Formation and Osteoclastogenesis Qiu, Minglong Li, Changwei Cai, Zhengwei Li, Cuidi Yang, Kai Tulufu, Nijiati Chen, Bo Cheng, Liang Zhuang, Chengyu Liu, Zhihong Qi, Jin Cui, Wenguo Deng, Lianfu Adv Sci (Weinh) Research Articles The formation of a calcified cartilaginous callus (CACC) is crucial during bone repair. CACC can stimulate the invasion of type H vessels into the callus to couple angiogenesis and osteogenesis, induce osteoclastogenesis to resorb the calcified matrix, and promote osteoclast secretion of factors to enhance osteogenesis, ultimately achieving the replacement of cartilage with bone. In this study, a porous polycaprolactone/hydroxyapatite‐iminodiacetic acid‐deferoxamine (PCL/HA‐SF‐DFO) 3D biomimetic CACC is developed using 3D printing. The porous structure can mimic the pores formed by the matrix metalloproteinase degradation of the cartilaginous matrix, HA‐containing PCL can mimic the calcified cartilaginous matrix, and SF anchors DFO onto HA for the slow release of DFO. The in vitro results show that the scaffold significantly enhances angiogenesis, promotes osteoclastogenesis and resorption by osteoclasts, and enhances the osteogenic differentiation of bone marrow stromal stem cells by promoting collagen triple helix repeat‐containing 1 expression by osteoclasts. The in vivo results show that the scaffold significantly promotes type H vessels formation and the expression of coupling factors to promote osteogenesis, ultimately enhancing the regeneration of large‐segment bone defects in rats and preventing dislodging of the internal fixation screw. In conclusion, the scaffold inspired by biological bone repair processes effectively promotes bone regeneration. John Wiley and Sons Inc. 2023-03-31 /pmc/articles/PMC10238192/ /pubmed/36999832 http://dx.doi.org/10.1002/advs.202207089 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
Qiu, Minglong
Li, Changwei
Cai, Zhengwei
Li, Cuidi
Yang, Kai
Tulufu, Nijiati
Chen, Bo
Cheng, Liang
Zhuang, Chengyu
Liu, Zhihong
Qi, Jin
Cui, Wenguo
Deng, Lianfu
3D Biomimetic Calcified Cartilaginous Callus that Induces Type H Vessels Formation and Osteoclastogenesis
title 3D Biomimetic Calcified Cartilaginous Callus that Induces Type H Vessels Formation and Osteoclastogenesis
title_full 3D Biomimetic Calcified Cartilaginous Callus that Induces Type H Vessels Formation and Osteoclastogenesis
title_fullStr 3D Biomimetic Calcified Cartilaginous Callus that Induces Type H Vessels Formation and Osteoclastogenesis
title_full_unstemmed 3D Biomimetic Calcified Cartilaginous Callus that Induces Type H Vessels Formation and Osteoclastogenesis
title_short 3D Biomimetic Calcified Cartilaginous Callus that Induces Type H Vessels Formation and Osteoclastogenesis
title_sort 3d biomimetic calcified cartilaginous callus that induces type h vessels formation and osteoclastogenesis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238192/
https://www.ncbi.nlm.nih.gov/pubmed/36999832
http://dx.doi.org/10.1002/advs.202207089
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