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Development and characterisation of a large diameter decellularised vascular allograft

The aims of this study were to develop a biological large diameter vascular graft by decellularisation of native human aorta to remove the immunogenic cells whilst retaining the essential biomechanical, and biochemical properties for the ultimate benefit of patients with infected synthetic grafts. D...

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Autores principales: Aldridge, A., Desai, A., Owston, H., Jennings, L. M., Fisher, J., Rooney, P., Kearney, J. N., Ingham, E., Wilshaw, S. P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133183/
https://www.ncbi.nlm.nih.gov/pubmed/29188402
http://dx.doi.org/10.1007/s10561-017-9673-y
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author Aldridge, A.
Desai, A.
Owston, H.
Jennings, L. M.
Fisher, J.
Rooney, P.
Kearney, J. N.
Ingham, E.
Wilshaw, S. P.
author_facet Aldridge, A.
Desai, A.
Owston, H.
Jennings, L. M.
Fisher, J.
Rooney, P.
Kearney, J. N.
Ingham, E.
Wilshaw, S. P.
author_sort Aldridge, A.
collection PubMed
description The aims of this study were to develop a biological large diameter vascular graft by decellularisation of native human aorta to remove the immunogenic cells whilst retaining the essential biomechanical, and biochemical properties for the ultimate benefit of patients with infected synthetic grafts. Donor aortas (n = 6) were subjected to an adaptation of a propriety decellularisation process to remove the cells and acellularity assessed by histological analysis and extraction and quantification of total DNA. The biocompatibility of the acellular aortas was determined using standard contact cytotoxicity tests. Collagen and denatured collagen content of aortas was determined and immunohistochemistry was used to determine the presence of specific extracellular matrix proteins. Donor aortas (n = 6) were divided into two, with one half subject to decellularisation and the other half retained as native tissue. The native and decellularised aorta sections were then subject to uniaxial tensile testing to failure [axial and circumferential directions] and suture retention testing. The data was compared using a paired t-test. Histological evaluation showed an absence of cells in the treated aortas and retention of histoarchitecture including elastin content. The decellularised aortas had less than 15 ng mg(−1) total DNA per dry weight (mean 94% reduction) and were biocompatible as determined by in vitro contact cytotoxicity tests. There were no gross changes in the histoarchitecture [elastin and collagen matrix] of the acellular aortas compared to native controls. The decellularisation process also reduced calcium deposits within the tissue. The uniaxial tensile and suture retention testing revealed no significant differences in the material properties (p > 0.05) of decellularised aorta. The decellularisation procedure resulted in minimal changes to the biological and biomechanical properties of the donor aortas. Acellular donor aorta has excellent potential for use as a large diameter vascular graft.
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spelling pubmed-61331832018-09-14 Development and characterisation of a large diameter decellularised vascular allograft Aldridge, A. Desai, A. Owston, H. Jennings, L. M. Fisher, J. Rooney, P. Kearney, J. N. Ingham, E. Wilshaw, S. P. Cell Tissue Bank Article The aims of this study were to develop a biological large diameter vascular graft by decellularisation of native human aorta to remove the immunogenic cells whilst retaining the essential biomechanical, and biochemical properties for the ultimate benefit of patients with infected synthetic grafts. Donor aortas (n = 6) were subjected to an adaptation of a propriety decellularisation process to remove the cells and acellularity assessed by histological analysis and extraction and quantification of total DNA. The biocompatibility of the acellular aortas was determined using standard contact cytotoxicity tests. Collagen and denatured collagen content of aortas was determined and immunohistochemistry was used to determine the presence of specific extracellular matrix proteins. Donor aortas (n = 6) were divided into two, with one half subject to decellularisation and the other half retained as native tissue. The native and decellularised aorta sections were then subject to uniaxial tensile testing to failure [axial and circumferential directions] and suture retention testing. The data was compared using a paired t-test. Histological evaluation showed an absence of cells in the treated aortas and retention of histoarchitecture including elastin content. The decellularised aortas had less than 15 ng mg(−1) total DNA per dry weight (mean 94% reduction) and were biocompatible as determined by in vitro contact cytotoxicity tests. There were no gross changes in the histoarchitecture [elastin and collagen matrix] of the acellular aortas compared to native controls. The decellularisation process also reduced calcium deposits within the tissue. The uniaxial tensile and suture retention testing revealed no significant differences in the material properties (p > 0.05) of decellularised aorta. The decellularisation procedure resulted in minimal changes to the biological and biomechanical properties of the donor aortas. Acellular donor aorta has excellent potential for use as a large diameter vascular graft. Springer Netherlands 2017-11-29 2018 /pmc/articles/PMC6133183/ /pubmed/29188402 http://dx.doi.org/10.1007/s10561-017-9673-y Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Article
Aldridge, A.
Desai, A.
Owston, H.
Jennings, L. M.
Fisher, J.
Rooney, P.
Kearney, J. N.
Ingham, E.
Wilshaw, S. P.
Development and characterisation of a large diameter decellularised vascular allograft
title Development and characterisation of a large diameter decellularised vascular allograft
title_full Development and characterisation of a large diameter decellularised vascular allograft
title_fullStr Development and characterisation of a large diameter decellularised vascular allograft
title_full_unstemmed Development and characterisation of a large diameter decellularised vascular allograft
title_short Development and characterisation of a large diameter decellularised vascular allograft
title_sort development and characterisation of a large diameter decellularised vascular allograft
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6133183/
https://www.ncbi.nlm.nih.gov/pubmed/29188402
http://dx.doi.org/10.1007/s10561-017-9673-y
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