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Interaction of micron and nano-sized particles with cells of the dura mater

Intervertebral total disc replacements (TDR) are used in the treatment of degenerative spinal disc disease. There are, however, concerns that they may be subject to long-term failure due to wear. The adverse effects of TDR wear have the potential to manifest in the dura mater and surrounding tissues...

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Autores principales: Papageorgiou, Iraklis, Marsh, Rainy, Tipper, Joanne L, Hall, Richard M, Fisher, John, Ingham, Eileen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4336564/
https://www.ncbi.nlm.nih.gov/pubmed/24604838
http://dx.doi.org/10.1002/jbm.b.33129
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author Papageorgiou, Iraklis
Marsh, Rainy
Tipper, Joanne L
Hall, Richard M
Fisher, John
Ingham, Eileen
author_facet Papageorgiou, Iraklis
Marsh, Rainy
Tipper, Joanne L
Hall, Richard M
Fisher, John
Ingham, Eileen
author_sort Papageorgiou, Iraklis
collection PubMed
description Intervertebral total disc replacements (TDR) are used in the treatment of degenerative spinal disc disease. There are, however, concerns that they may be subject to long-term failure due to wear. The adverse effects of TDR wear have the potential to manifest in the dura mater and surrounding tissues. The aim of this study was to investigate the physiological structure of the dura mater, isolate the resident dural epithelial and stromal cells and analyse the capacity of these cells to internalise model polymer particles. The porcine dura mater was a collagen-rich structure encompassing regularly arranged fibroblastic cells within an outermost epithelial cell layer. The isolated dural epithelial cells had endothelial cell characteristics (positive for von Willebrand factor, CD31, E-cadherin and desmoplakin) and barrier functionality whereas the fibroblastic cells were positive for collagen I and III, tenascin and actin. The capacity of the dural cells to take up model particles was dependent on particle size. Nanometer sized particles readily penetrated both types of cells. However, dural fibroblasts engulfed micron-sized particles at a much higher rate than dural epithelial cells. The study suggested that dural epithelial cells may offer some barrier to the penetration of micron-sized particles but not nanometer sized particles. © 2014 The Authors. Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 102B: 1496–1505, 2014.
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spelling pubmed-43365642015-03-04 Interaction of micron and nano-sized particles with cells of the dura mater Papageorgiou, Iraklis Marsh, Rainy Tipper, Joanne L Hall, Richard M Fisher, John Ingham, Eileen J Biomed Mater Res B Appl Biomater Original Research Reports Intervertebral total disc replacements (TDR) are used in the treatment of degenerative spinal disc disease. There are, however, concerns that they may be subject to long-term failure due to wear. The adverse effects of TDR wear have the potential to manifest in the dura mater and surrounding tissues. The aim of this study was to investigate the physiological structure of the dura mater, isolate the resident dural epithelial and stromal cells and analyse the capacity of these cells to internalise model polymer particles. The porcine dura mater was a collagen-rich structure encompassing regularly arranged fibroblastic cells within an outermost epithelial cell layer. The isolated dural epithelial cells had endothelial cell characteristics (positive for von Willebrand factor, CD31, E-cadherin and desmoplakin) and barrier functionality whereas the fibroblastic cells were positive for collagen I and III, tenascin and actin. The capacity of the dural cells to take up model particles was dependent on particle size. Nanometer sized particles readily penetrated both types of cells. However, dural fibroblasts engulfed micron-sized particles at a much higher rate than dural epithelial cells. The study suggested that dural epithelial cells may offer some barrier to the penetration of micron-sized particles but not nanometer sized particles. © 2014 The Authors. Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 102B: 1496–1505, 2014. BlackWell Publishing Ltd 2014-10 2014-03-06 /pmc/articles/PMC4336564/ /pubmed/24604838 http://dx.doi.org/10.1002/jbm.b.33129 Text en © 2014 The Authors. Journal of Biomedical Materials Research Part B: Applied Biomaterials Published by Wiley Periodicals, Inc. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Reports
Papageorgiou, Iraklis
Marsh, Rainy
Tipper, Joanne L
Hall, Richard M
Fisher, John
Ingham, Eileen
Interaction of micron and nano-sized particles with cells of the dura mater
title Interaction of micron and nano-sized particles with cells of the dura mater
title_full Interaction of micron and nano-sized particles with cells of the dura mater
title_fullStr Interaction of micron and nano-sized particles with cells of the dura mater
title_full_unstemmed Interaction of micron and nano-sized particles with cells of the dura mater
title_short Interaction of micron and nano-sized particles with cells of the dura mater
title_sort interaction of micron and nano-sized particles with cells of the dura mater
topic Original Research Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4336564/
https://www.ncbi.nlm.nih.gov/pubmed/24604838
http://dx.doi.org/10.1002/jbm.b.33129
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