Growth plate extracellular matrix-derived scaffolds for large bone defect healing

Limitations associated with demineralised bone matrix and other grafting materials have motivated the development of alternative strategies to enhance the repair of large bone defects. The growth plate (GP) of developing limbs contain a plethora of growth factors and matrix cues which contribute to...

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Main Authors: GM Cunniffe, PJ Díaz-Payno, JS Ramey, OR Mahon, A Dunne, EM Thompson, FJ O’Brien, DJ Kelly
Format: Article
Language:English
Published: AO Research Institute Davos 2017-02-01
Series:European Cells & Materials
Subjects:
Online Access:http://www.ecmjournal.org/papers/vol033/pdf/v033a10.pdf
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spelling doaj-bc10fc5177e648a293c8c403e89cd2292020-11-24T20:44:35Zeng AO Research Institute DavosEuropean Cells & Materials1473-22622017-02-013313014210.22203/eCM.v033a10Growth plate extracellular matrix-derived scaffolds for large bone defect healingGM CunniffePJ Díaz-PaynoJS RameyOR MahonA DunneEM ThompsonFJ O’BrienDJ Kelly0Trinity Centre for Bioengineering, Trinity Biomedical Sciences Institute, 152-160 Pearse Street, Dublin 2, IrelandLimitations associated with demineralised bone matrix and other grafting materials have motivated the development of alternative strategies to enhance the repair of large bone defects. The growth plate (GP) of developing limbs contain a plethora of growth factors and matrix cues which contribute to long bone growth, suggesting that biomaterials derived from its extracellular matrix (ECM) may be uniquely suited to promoting bone regeneration. The goal of this study was to generate porous scaffolds from decellularised GP ECM and to evaluate their ability to enhance host mediated bone regeneration following their implantation into critically-sized rat cranial defects. The scaffolds were first assessed by culturing with primary human macrophages, which demonstrated that decellularisation resulted in reduced IL-1β and IL-8 production. In vitro, GP derived scaffolds were found capable of supporting osteogenesis of mesenchymal stem cells via either an intramembranous or an endochondral pathway, demonstrating the intrinsic osteoinductivity of the biomaterial. Furthermore, upon implantation into cranial defects, GP derived scaffolds were observed to accelerate vessel in-growth, mineralisation and de novo bone formation. These results support the use of decellularised GP ECM as a scaffold for large bone defect regeneration. http://www.ecmjournal.org/papers/vol033/pdf/v033a10.pdfGrowth plateextracellular matrixscaffoldlarge bone defect regeneration
collection DOAJ
language English
format Article
sources DOAJ
author GM Cunniffe
PJ Díaz-Payno
JS Ramey
OR Mahon
A Dunne
EM Thompson
FJ O’Brien
DJ Kelly
spellingShingle GM Cunniffe
PJ Díaz-Payno
JS Ramey
OR Mahon
A Dunne
EM Thompson
FJ O’Brien
DJ Kelly
Growth plate extracellular matrix-derived scaffolds for large bone defect healing
European Cells & Materials
Growth plate
extracellular matrix
scaffold
large bone defect regeneration
author_facet GM Cunniffe
PJ Díaz-Payno
JS Ramey
OR Mahon
A Dunne
EM Thompson
FJ O’Brien
DJ Kelly
author_sort GM Cunniffe
title Growth plate extracellular matrix-derived scaffolds for large bone defect healing
title_short Growth plate extracellular matrix-derived scaffolds for large bone defect healing
title_full Growth plate extracellular matrix-derived scaffolds for large bone defect healing
title_fullStr Growth plate extracellular matrix-derived scaffolds for large bone defect healing
title_full_unstemmed Growth plate extracellular matrix-derived scaffolds for large bone defect healing
title_sort growth plate extracellular matrix-derived scaffolds for large bone defect healing
publisher AO Research Institute Davos
series European Cells & Materials
issn 1473-2262
publishDate 2017-02-01
description Limitations associated with demineralised bone matrix and other grafting materials have motivated the development of alternative strategies to enhance the repair of large bone defects. The growth plate (GP) of developing limbs contain a plethora of growth factors and matrix cues which contribute to long bone growth, suggesting that biomaterials derived from its extracellular matrix (ECM) may be uniquely suited to promoting bone regeneration. The goal of this study was to generate porous scaffolds from decellularised GP ECM and to evaluate their ability to enhance host mediated bone regeneration following their implantation into critically-sized rat cranial defects. The scaffolds were first assessed by culturing with primary human macrophages, which demonstrated that decellularisation resulted in reduced IL-1β and IL-8 production. In vitro, GP derived scaffolds were found capable of supporting osteogenesis of mesenchymal stem cells via either an intramembranous or an endochondral pathway, demonstrating the intrinsic osteoinductivity of the biomaterial. Furthermore, upon implantation into cranial defects, GP derived scaffolds were observed to accelerate vessel in-growth, mineralisation and de novo bone formation. These results support the use of decellularised GP ECM as a scaffold for large bone defect regeneration.
topic Growth plate
extracellular matrix
scaffold
large bone defect regeneration
url http://www.ecmjournal.org/papers/vol033/pdf/v033a10.pdf
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