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Vascularized bone regeneration accelerated by 3D-printed nanosilicate-functionalized polycaprolactone scaffold

Critical oral-maxillofacial bone defects, damaged by trauma and tumors, not only affect the physiological functions and mental health of patients but are also highly challenging to reconstruct. Personalized biomaterials customized by 3D printing technology have the potential to match oral-maxillofac...

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Autores principales: Xu, Xiongcheng, Xiao, Long, Xu, Yanmei, Zhuo, Jin, Yang, Xue, Li, Li, Xiao, Nianqi, Tao, Jing, Zhong, Quan, Li, Yanfen, Chen, Yuling, Du, Zhibin, Luo, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633727/
https://www.ncbi.nlm.nih.gov/pubmed/34858634
http://dx.doi.org/10.1093/rb/rbab061
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author Xu, Xiongcheng
Xiao, Long
Xu, Yanmei
Zhuo, Jin
Yang, Xue
Li, Li
Xiao, Nianqi
Tao, Jing
Zhong, Quan
Li, Yanfen
Chen, Yuling
Du, Zhibin
Luo, Kai
author_facet Xu, Xiongcheng
Xiao, Long
Xu, Yanmei
Zhuo, Jin
Yang, Xue
Li, Li
Xiao, Nianqi
Tao, Jing
Zhong, Quan
Li, Yanfen
Chen, Yuling
Du, Zhibin
Luo, Kai
author_sort Xu, Xiongcheng
collection PubMed
description Critical oral-maxillofacial bone defects, damaged by trauma and tumors, not only affect the physiological functions and mental health of patients but are also highly challenging to reconstruct. Personalized biomaterials customized by 3D printing technology have the potential to match oral-maxillofacial bone repair and regeneration requirements. Laponite (LAP) nanosilicates have been added to biomaterials to achieve biofunctional modification owing to their excellent biocompatibility and bioactivity. Herein, porous nanosilicate-functionalized polycaprolactone (PCL/LAP) was fabricated by 3D printing technology, and its bioactivities in bone regeneration were investigated in vitro and in vivo. In vitro experiments demonstrated that PCL/LAP exhibited good cytocompatibility and enhanced the viability of bone marrow mesenchymal stem cells (BMSCs). PCL/LAP functioned to stimulate osteogenic differentiation of BMSCs at the mRNA and protein levels and elevated angiogenic gene expression and cytokine secretion. Moreover, BMSCs cultured on PCL/LAP promoted the angiogenesis potential of endothelial cells by angiogenic cytokine secretion. Then, PCL/LAP scaffolds were implanted into the calvarial defect model. Toxicological safety of PCL/LAP was confirmed, and significant enhancement of vascularized bone formation was observed. Taken together, 3D-printed PCL/LAP scaffolds with brilliant osteogenesis to enhance bone regeneration could be envisaged as an outstanding bone substitute for a promising change in oral-maxillofacial bone defect reconstruction.
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spelling pubmed-86337272021-12-01 Vascularized bone regeneration accelerated by 3D-printed nanosilicate-functionalized polycaprolactone scaffold Xu, Xiongcheng Xiao, Long Xu, Yanmei Zhuo, Jin Yang, Xue Li, Li Xiao, Nianqi Tao, Jing Zhong, Quan Li, Yanfen Chen, Yuling Du, Zhibin Luo, Kai Regen Biomater Research Article Critical oral-maxillofacial bone defects, damaged by trauma and tumors, not only affect the physiological functions and mental health of patients but are also highly challenging to reconstruct. Personalized biomaterials customized by 3D printing technology have the potential to match oral-maxillofacial bone repair and regeneration requirements. Laponite (LAP) nanosilicates have been added to biomaterials to achieve biofunctional modification owing to their excellent biocompatibility and bioactivity. Herein, porous nanosilicate-functionalized polycaprolactone (PCL/LAP) was fabricated by 3D printing technology, and its bioactivities in bone regeneration were investigated in vitro and in vivo. In vitro experiments demonstrated that PCL/LAP exhibited good cytocompatibility and enhanced the viability of bone marrow mesenchymal stem cells (BMSCs). PCL/LAP functioned to stimulate osteogenic differentiation of BMSCs at the mRNA and protein levels and elevated angiogenic gene expression and cytokine secretion. Moreover, BMSCs cultured on PCL/LAP promoted the angiogenesis potential of endothelial cells by angiogenic cytokine secretion. Then, PCL/LAP scaffolds were implanted into the calvarial defect model. Toxicological safety of PCL/LAP was confirmed, and significant enhancement of vascularized bone formation was observed. Taken together, 3D-printed PCL/LAP scaffolds with brilliant osteogenesis to enhance bone regeneration could be envisaged as an outstanding bone substitute for a promising change in oral-maxillofacial bone defect reconstruction. Oxford University Press 2021-11-12 /pmc/articles/PMC8633727/ /pubmed/34858634 http://dx.doi.org/10.1093/rb/rbab061 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://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 Article
Xu, Xiongcheng
Xiao, Long
Xu, Yanmei
Zhuo, Jin
Yang, Xue
Li, Li
Xiao, Nianqi
Tao, Jing
Zhong, Quan
Li, Yanfen
Chen, Yuling
Du, Zhibin
Luo, Kai
Vascularized bone regeneration accelerated by 3D-printed nanosilicate-functionalized polycaprolactone scaffold
title Vascularized bone regeneration accelerated by 3D-printed nanosilicate-functionalized polycaprolactone scaffold
title_full Vascularized bone regeneration accelerated by 3D-printed nanosilicate-functionalized polycaprolactone scaffold
title_fullStr Vascularized bone regeneration accelerated by 3D-printed nanosilicate-functionalized polycaprolactone scaffold
title_full_unstemmed Vascularized bone regeneration accelerated by 3D-printed nanosilicate-functionalized polycaprolactone scaffold
title_short Vascularized bone regeneration accelerated by 3D-printed nanosilicate-functionalized polycaprolactone scaffold
title_sort vascularized bone regeneration accelerated by 3d-printed nanosilicate-functionalized polycaprolactone scaffold
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8633727/
https://www.ncbi.nlm.nih.gov/pubmed/34858634
http://dx.doi.org/10.1093/rb/rbab061
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