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Prefabrication of a functional bone graft with a pedicled periosteal flap as an in vivo bioreactor
The in vivo bioreactor principle, which focuses on using the body as a living bioreactor to cultivate stem cells, bioscaffolds, and growth factors and leveraging the body’s self-regenerative capacity to regenerate new tissue, has been considered a potential approach for bone defect reconstruction. T...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740121/ https://www.ncbi.nlm.nih.gov/pubmed/29269864 http://dx.doi.org/10.1038/s41598-017-17452-5 |
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author | Huang, Ru-Lin Tremp, Mathias Ho, Chia-Kang Sun, Yangbai Liu, Kai Li, Qingfeng |
author_facet | Huang, Ru-Lin Tremp, Mathias Ho, Chia-Kang Sun, Yangbai Liu, Kai Li, Qingfeng |
author_sort | Huang, Ru-Lin |
collection | PubMed |
description | The in vivo bioreactor principle, which focuses on using the body as a living bioreactor to cultivate stem cells, bioscaffolds, and growth factors and leveraging the body’s self-regenerative capacity to regenerate new tissue, has been considered a potential approach for bone defect reconstruction. The histological characteristics of the periosteum allow it to possess a remarkable capacity to induce bone growth and remodeling, making it suitable as an in vivo bioreactor strategy for bone graft prefabrication. The present study was designed to prefabricate vascularized bone grafts using pedicled periosteal flaps and decellularized bone matrix (DBM) scaffolds in a rabbit model. The muscular pouches created in the femoral muscle were acted as a control. Our histological results revealed that both the periosteal flap group and muscular pouch group induced bone tissue formation on the DBM surface at both 8 and 16 weeks postoperatively. However, micro-computed tomography (microCT) scanning, biomechanical, and histomorphometric findings indicated that bone grafts from the periosteal flap group showed larger bone mass, faster bone formation rates, higher vascular density, and stronger biomechanical properties than in the muscular pouch group. We suggest that using the pedicled periosteal flap as an in vivo bioreactor is a promising approach for functional bone graft prefabrication. |
format | Online Article Text |
id | pubmed-5740121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-57401212018-01-03 Prefabrication of a functional bone graft with a pedicled periosteal flap as an in vivo bioreactor Huang, Ru-Lin Tremp, Mathias Ho, Chia-Kang Sun, Yangbai Liu, Kai Li, Qingfeng Sci Rep Article The in vivo bioreactor principle, which focuses on using the body as a living bioreactor to cultivate stem cells, bioscaffolds, and growth factors and leveraging the body’s self-regenerative capacity to regenerate new tissue, has been considered a potential approach for bone defect reconstruction. The histological characteristics of the periosteum allow it to possess a remarkable capacity to induce bone growth and remodeling, making it suitable as an in vivo bioreactor strategy for bone graft prefabrication. The present study was designed to prefabricate vascularized bone grafts using pedicled periosteal flaps and decellularized bone matrix (DBM) scaffolds in a rabbit model. The muscular pouches created in the femoral muscle were acted as a control. Our histological results revealed that both the periosteal flap group and muscular pouch group induced bone tissue formation on the DBM surface at both 8 and 16 weeks postoperatively. However, micro-computed tomography (microCT) scanning, biomechanical, and histomorphometric findings indicated that bone grafts from the periosteal flap group showed larger bone mass, faster bone formation rates, higher vascular density, and stronger biomechanical properties than in the muscular pouch group. We suggest that using the pedicled periosteal flap as an in vivo bioreactor is a promising approach for functional bone graft prefabrication. Nature Publishing Group UK 2017-12-21 /pmc/articles/PMC5740121/ /pubmed/29269864 http://dx.doi.org/10.1038/s41598-017-17452-5 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Huang, Ru-Lin Tremp, Mathias Ho, Chia-Kang Sun, Yangbai Liu, Kai Li, Qingfeng Prefabrication of a functional bone graft with a pedicled periosteal flap as an in vivo bioreactor |
title | Prefabrication of a functional bone graft with a pedicled periosteal flap as an in vivo bioreactor |
title_full | Prefabrication of a functional bone graft with a pedicled periosteal flap as an in vivo bioreactor |
title_fullStr | Prefabrication of a functional bone graft with a pedicled periosteal flap as an in vivo bioreactor |
title_full_unstemmed | Prefabrication of a functional bone graft with a pedicled periosteal flap as an in vivo bioreactor |
title_short | Prefabrication of a functional bone graft with a pedicled periosteal flap as an in vivo bioreactor |
title_sort | prefabrication of a functional bone graft with a pedicled periosteal flap as an in vivo bioreactor |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740121/ https://www.ncbi.nlm.nih.gov/pubmed/29269864 http://dx.doi.org/10.1038/s41598-017-17452-5 |
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