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Restoration of a Critical Mandibular Bone Defect Using Human Alveolar Bone-Derived Stem Cells and Porous Nano-HA/Collagen/PLA Scaffold

Periodontal bone defects occur in a wide variety of clinical situations. Adult stem cell- and biomaterial-based bone tissue regeneration are a promising alternative to natural bone grafts. Recent evidence has demonstrated that two populations of adult bone marrow mesenchymal stromal cells (BMSCs) ca...

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Autores principales: Wang, Xing, Xing, Helin, Zhang, Guilan, Wu, Xia, Zou, Xuan, Feng, Lin, Wang, Dongsheng, Li, Meng, Zhao, Jing, Du, Jianwei, Lv, Yan, E, Lingling, Liu, Hongchen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826948/
https://www.ncbi.nlm.nih.gov/pubmed/27118977
http://dx.doi.org/10.1155/2016/8741641
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author Wang, Xing
Xing, Helin
Zhang, Guilan
Wu, Xia
Zou, Xuan
Feng, Lin
Wang, Dongsheng
Li, Meng
Zhao, Jing
Du, Jianwei
Lv, Yan
E, Lingling
Liu, Hongchen
author_facet Wang, Xing
Xing, Helin
Zhang, Guilan
Wu, Xia
Zou, Xuan
Feng, Lin
Wang, Dongsheng
Li, Meng
Zhao, Jing
Du, Jianwei
Lv, Yan
E, Lingling
Liu, Hongchen
author_sort Wang, Xing
collection PubMed
description Periodontal bone defects occur in a wide variety of clinical situations. Adult stem cell- and biomaterial-based bone tissue regeneration are a promising alternative to natural bone grafts. Recent evidence has demonstrated that two populations of adult bone marrow mesenchymal stromal cells (BMSCs) can be distinguished based on their embryonic origins. These BMSCs are not interchangeable, as bones preferentially heal using cells that share the same embryonic origin. However, the feasibility of tissue engineering using human craniofacial BMSCs was unclear. The goal of this study was to explore human craniofacial BMSC-based therapy for the treatment of localized mandibular defects using a standardized, minimally invasive procedure. The BMSCs' identity was confirmed. Scanning electron microscopy, a cell proliferation assay, and supernatant detection indicated that the nHAC/PLA provided a suitable environment for aBMSCs. Real-time PCR and electrochemiluminescence immunoassays demonstrated that osteogenic markers were upregulated by osteogenic preinduction. Moreover, in a rabbit critical-size mandibular bone defect model, total bone formation in the nHAC/PLA + aBMSCs group was significantly higher than in the nHAC/PLA group but significantly lower than in the nHAC/PLA + preinduced aBMSCs. These findings demonstrate that this engineered bone is a valid alternative for the correction of mandibular bone defects.
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spelling pubmed-48269482016-04-26 Restoration of a Critical Mandibular Bone Defect Using Human Alveolar Bone-Derived Stem Cells and Porous Nano-HA/Collagen/PLA Scaffold Wang, Xing Xing, Helin Zhang, Guilan Wu, Xia Zou, Xuan Feng, Lin Wang, Dongsheng Li, Meng Zhao, Jing Du, Jianwei Lv, Yan E, Lingling Liu, Hongchen Stem Cells Int Research Article Periodontal bone defects occur in a wide variety of clinical situations. Adult stem cell- and biomaterial-based bone tissue regeneration are a promising alternative to natural bone grafts. Recent evidence has demonstrated that two populations of adult bone marrow mesenchymal stromal cells (BMSCs) can be distinguished based on their embryonic origins. These BMSCs are not interchangeable, as bones preferentially heal using cells that share the same embryonic origin. However, the feasibility of tissue engineering using human craniofacial BMSCs was unclear. The goal of this study was to explore human craniofacial BMSC-based therapy for the treatment of localized mandibular defects using a standardized, minimally invasive procedure. The BMSCs' identity was confirmed. Scanning electron microscopy, a cell proliferation assay, and supernatant detection indicated that the nHAC/PLA provided a suitable environment for aBMSCs. Real-time PCR and electrochemiluminescence immunoassays demonstrated that osteogenic markers were upregulated by osteogenic preinduction. Moreover, in a rabbit critical-size mandibular bone defect model, total bone formation in the nHAC/PLA + aBMSCs group was significantly higher than in the nHAC/PLA group but significantly lower than in the nHAC/PLA + preinduced aBMSCs. These findings demonstrate that this engineered bone is a valid alternative for the correction of mandibular bone defects. Hindawi Publishing Corporation 2016 2016-03-28 /pmc/articles/PMC4826948/ /pubmed/27118977 http://dx.doi.org/10.1155/2016/8741641 Text en Copyright © 2016 Xing Wang et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Xing
Xing, Helin
Zhang, Guilan
Wu, Xia
Zou, Xuan
Feng, Lin
Wang, Dongsheng
Li, Meng
Zhao, Jing
Du, Jianwei
Lv, Yan
E, Lingling
Liu, Hongchen
Restoration of a Critical Mandibular Bone Defect Using Human Alveolar Bone-Derived Stem Cells and Porous Nano-HA/Collagen/PLA Scaffold
title Restoration of a Critical Mandibular Bone Defect Using Human Alveolar Bone-Derived Stem Cells and Porous Nano-HA/Collagen/PLA Scaffold
title_full Restoration of a Critical Mandibular Bone Defect Using Human Alveolar Bone-Derived Stem Cells and Porous Nano-HA/Collagen/PLA Scaffold
title_fullStr Restoration of a Critical Mandibular Bone Defect Using Human Alveolar Bone-Derived Stem Cells and Porous Nano-HA/Collagen/PLA Scaffold
title_full_unstemmed Restoration of a Critical Mandibular Bone Defect Using Human Alveolar Bone-Derived Stem Cells and Porous Nano-HA/Collagen/PLA Scaffold
title_short Restoration of a Critical Mandibular Bone Defect Using Human Alveolar Bone-Derived Stem Cells and Porous Nano-HA/Collagen/PLA Scaffold
title_sort restoration of a critical mandibular bone defect using human alveolar bone-derived stem cells and porous nano-ha/collagen/pla scaffold
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826948/
https://www.ncbi.nlm.nih.gov/pubmed/27118977
http://dx.doi.org/10.1155/2016/8741641
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