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Decellularized bone matrix grafts for calvaria regeneration

Decellularization is a promising new method to prepare natural matrices for tissue regeneration. Successful decellularization has been reported using various tissues including skin, tendon, and cartilage, though studies using hard tissue such as bone are lacking. In this study, we aimed to define th...

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Autores principales: Lee, Dong Joon, Diachina, Shannon, Lee, Yan Ting, Zhao, Lixing, Zou, Rui, Tang, Na, Han, Han, Chen, Xin, Ko, Ching-Chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308431/
https://www.ncbi.nlm.nih.gov/pubmed/28228929
http://dx.doi.org/10.1177/2041731416680306
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author Lee, Dong Joon
Diachina, Shannon
Lee, Yan Ting
Zhao, Lixing
Zou, Rui
Tang, Na
Han, Han
Chen, Xin
Ko, Ching-Chang
author_facet Lee, Dong Joon
Diachina, Shannon
Lee, Yan Ting
Zhao, Lixing
Zou, Rui
Tang, Na
Han, Han
Chen, Xin
Ko, Ching-Chang
author_sort Lee, Dong Joon
collection PubMed
description Decellularization is a promising new method to prepare natural matrices for tissue regeneration. Successful decellularization has been reported using various tissues including skin, tendon, and cartilage, though studies using hard tissue such as bone are lacking. In this study, we aimed to define the optimal experimental parameters to decellularize natural bone matrix using 0.5% sodium dodecyl sulfate and 0.1% NH(4)OH. Then, the effects of decellularized bone matrix on rat mesenchymal stem cell proliferation, osteogenic gene expression, and osteogenic differentiations in a two-dimensional culture system were investigated. Decellularized bone was also evaluated with regard to cytotoxicity, biochemical, and mechanical characteristics in vitro. Evidence of complete decellularization was shown through hematoxylin and eosin staining and DNA measurements. Decellularized bone matrix displayed a cytocompatible property, conserved structure, mechanical strength, and mineral content comparable to natural bone. To study new bone formation, implantation of decellularized bone matrix particles seeded with rat mesenchymal stem cells was conducted using an orthotopic in vivo model. After 3 months post-implantation into a critical-sized defect in rat calvaria, new bone was formed around decellularized bone matrix particles and also merged with new bone between decellularized bone matrix particles. New bone formation was analyzed with micro computed tomography, mineral apposition rate, and histomorphometry. Decellularized bone matrix stimulated mesenchymal stem cell proliferation and osteogenic differentiation in vitro and in vivo, achieving effective bone regeneration and thereby serving as a promising biological bone graft.
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spelling pubmed-53084312017-02-22 Decellularized bone matrix grafts for calvaria regeneration Lee, Dong Joon Diachina, Shannon Lee, Yan Ting Zhao, Lixing Zou, Rui Tang, Na Han, Han Chen, Xin Ko, Ching-Chang J Tissue Eng Multifaceted Therapeutic Systems for Tissue Regeneration Decellularization is a promising new method to prepare natural matrices for tissue regeneration. Successful decellularization has been reported using various tissues including skin, tendon, and cartilage, though studies using hard tissue such as bone are lacking. In this study, we aimed to define the optimal experimental parameters to decellularize natural bone matrix using 0.5% sodium dodecyl sulfate and 0.1% NH(4)OH. Then, the effects of decellularized bone matrix on rat mesenchymal stem cell proliferation, osteogenic gene expression, and osteogenic differentiations in a two-dimensional culture system were investigated. Decellularized bone was also evaluated with regard to cytotoxicity, biochemical, and mechanical characteristics in vitro. Evidence of complete decellularization was shown through hematoxylin and eosin staining and DNA measurements. Decellularized bone matrix displayed a cytocompatible property, conserved structure, mechanical strength, and mineral content comparable to natural bone. To study new bone formation, implantation of decellularized bone matrix particles seeded with rat mesenchymal stem cells was conducted using an orthotopic in vivo model. After 3 months post-implantation into a critical-sized defect in rat calvaria, new bone was formed around decellularized bone matrix particles and also merged with new bone between decellularized bone matrix particles. New bone formation was analyzed with micro computed tomography, mineral apposition rate, and histomorphometry. Decellularized bone matrix stimulated mesenchymal stem cell proliferation and osteogenic differentiation in vitro and in vivo, achieving effective bone regeneration and thereby serving as a promising biological bone graft. SAGE Publications 2016-12-05 /pmc/articles/PMC5308431/ /pubmed/28228929 http://dx.doi.org/10.1177/2041731416680306 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page(https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Multifaceted Therapeutic Systems for Tissue Regeneration
Lee, Dong Joon
Diachina, Shannon
Lee, Yan Ting
Zhao, Lixing
Zou, Rui
Tang, Na
Han, Han
Chen, Xin
Ko, Ching-Chang
Decellularized bone matrix grafts for calvaria regeneration
title Decellularized bone matrix grafts for calvaria regeneration
title_full Decellularized bone matrix grafts for calvaria regeneration
title_fullStr Decellularized bone matrix grafts for calvaria regeneration
title_full_unstemmed Decellularized bone matrix grafts for calvaria regeneration
title_short Decellularized bone matrix grafts for calvaria regeneration
title_sort decellularized bone matrix grafts for calvaria regeneration
topic Multifaceted Therapeutic Systems for Tissue Regeneration
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5308431/
https://www.ncbi.nlm.nih.gov/pubmed/28228929
http://dx.doi.org/10.1177/2041731416680306
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