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Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage
Currently, autologous chondrocyte implantation (ACI) is the most commonly used cell-based therapy for the treatment of isolated femoral condyle lesions of the knee. A small number of centres performing ACI have reported encouraging long-term clinical results, but there is currently a lack of quantit...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206378/ https://www.ncbi.nlm.nih.gov/pubmed/17697352 http://dx.doi.org/10.1186/ar2278 |
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author | Sharma, Aarti Wood, Lindsay D Richardson, James B Roberts, Sally Kuiper, Nicola J |
author_facet | Sharma, Aarti Wood, Lindsay D Richardson, James B Roberts, Sally Kuiper, Nicola J |
author_sort | Sharma, Aarti |
collection | PubMed |
description | Currently, autologous chondrocyte implantation (ACI) is the most commonly used cell-based therapy for the treatment of isolated femoral condyle lesions of the knee. A small number of centres performing ACI have reported encouraging long-term clinical results, but there is currently a lack of quantitative and qualitative biochemical data regarding the nature of the repair tissue. Glycosaminoglycan (GAG) structure influences physiological function and is likely to be important in the long-term stability of the repair tissue. The objective of this study was to use fluorophore-assisted carbohydrate electrophoresis (FACE) to both quantitatively and qualitatively analyse the GAG composition of repair tissue biopsies and compare them with age-matched cadaveric controls. We used immunohistochemistry to provide a baseline reference for comparison. Biopsies were taken from eight patients (22 to 52 years old) 1 year after ACI treatment and from four cadavers (20 to 50 years old). FACE quantitatively profiled the GAGs in as little as 5 μg of cartilage. The pattern and intensity of immunostaining were generally comparable with the data obtained with FACE. In the ACI repair tissue, there was a twofold reduction in chondroitin sulphate and keratan sulphate compared with age-matched control cartilage. By contrast, there was an increase in hyaluronan with significantly shorter chondroitin sulphate chains and less chondroitin 6-sulphate in repair tissue than control cartilage. The composition of the repair tissue thus is not identical to mature articular cartilage. |
format | Text |
id | pubmed-2206378 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-22063782008-01-19 Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage Sharma, Aarti Wood, Lindsay D Richardson, James B Roberts, Sally Kuiper, Nicola J Arthritis Res Ther Research Article Currently, autologous chondrocyte implantation (ACI) is the most commonly used cell-based therapy for the treatment of isolated femoral condyle lesions of the knee. A small number of centres performing ACI have reported encouraging long-term clinical results, but there is currently a lack of quantitative and qualitative biochemical data regarding the nature of the repair tissue. Glycosaminoglycan (GAG) structure influences physiological function and is likely to be important in the long-term stability of the repair tissue. The objective of this study was to use fluorophore-assisted carbohydrate electrophoresis (FACE) to both quantitatively and qualitatively analyse the GAG composition of repair tissue biopsies and compare them with age-matched cadaveric controls. We used immunohistochemistry to provide a baseline reference for comparison. Biopsies were taken from eight patients (22 to 52 years old) 1 year after ACI treatment and from four cadavers (20 to 50 years old). FACE quantitatively profiled the GAGs in as little as 5 μg of cartilage. The pattern and intensity of immunostaining were generally comparable with the data obtained with FACE. In the ACI repair tissue, there was a twofold reduction in chondroitin sulphate and keratan sulphate compared with age-matched control cartilage. By contrast, there was an increase in hyaluronan with significantly shorter chondroitin sulphate chains and less chondroitin 6-sulphate in repair tissue than control cartilage. The composition of the repair tissue thus is not identical to mature articular cartilage. BioMed Central 2007 2007-08-14 /pmc/articles/PMC2206378/ /pubmed/17697352 http://dx.doi.org/10.1186/ar2278 Text en Copyright © 2007 Sharma et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Sharma, Aarti Wood, Lindsay D Richardson, James B Roberts, Sally Kuiper, Nicola J Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage |
title | Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage |
title_full | Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage |
title_fullStr | Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage |
title_full_unstemmed | Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage |
title_short | Glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage |
title_sort | glycosaminoglycan profiles of repair tissue formed following autologous chondrocyte implantation differ from control cartilage |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2206378/ https://www.ncbi.nlm.nih.gov/pubmed/17697352 http://dx.doi.org/10.1186/ar2278 |
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