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Chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair – effect of BMP-2

BACKGROUND: Articular cartilage has little capacity for repair in vivo, however, a small number of studies have shown that, in vitro, a damage/repair response can be induced. Recent work by our group has shown that cartilage can respond to single impact load and culture by producing repair cells on...

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Detalles Bibliográficos
Autores principales: Henson, Frances MD, Vincent, Thea
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2244625/
https://www.ncbi.nlm.nih.gov/pubmed/18053249
http://dx.doi.org/10.1186/1471-2474-8-120
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author Henson, Frances MD
Vincent, Thea
author_facet Henson, Frances MD
Vincent, Thea
author_sort Henson, Frances MD
collection PubMed
description BACKGROUND: Articular cartilage has little capacity for repair in vivo, however, a small number of studies have shown that, in vitro, a damage/repair response can be induced. Recent work by our group has shown that cartilage can respond to single impact load and culture by producing repair cells on the articular surface. The purpose of this study was to identify whether chondrocyte outgrowth into a 3D scaffold could be observed following single impact load and culture. The effect of bone morphogenic-2 (BMP-2) on this process was investigated. METHODS: Cartilage explants were single impact loaded, placed within a scaffold and cultured for up to 20 days +/- BMP-2. Cell numbers in the scaffold, on and extruding from the articular surface were quantified and the immunohistochemistry used to identify the cellular phenotype. RESULTS: Following single impact load and culture, chondrocytes were observed in a 3D gelatin scaffold under all culture conditions. Chondrocytes were also observed on the articular surface of the cartilage and extruding out of the parent cartilage and on to the cartilage surface. BMP-2 was demonstrated to quantitatively inhibit these events. CONCLUSION: These studies demonstrate that articular chondrocytes can be stimulated to migrate out of parent cartilage following single impact load and culture. The addition of BMP-2 to the culture medium quantitatively reduced the repair response. It may be that the inhibitory effect of BMP-2 in this experimental model provides a clue to the apparent inability of articular cartilage to heal itself following damage in vivo.
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spelling pubmed-22446252008-02-15 Chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair – effect of BMP-2 Henson, Frances MD Vincent, Thea BMC Musculoskelet Disord Research Article BACKGROUND: Articular cartilage has little capacity for repair in vivo, however, a small number of studies have shown that, in vitro, a damage/repair response can be induced. Recent work by our group has shown that cartilage can respond to single impact load and culture by producing repair cells on the articular surface. The purpose of this study was to identify whether chondrocyte outgrowth into a 3D scaffold could be observed following single impact load and culture. The effect of bone morphogenic-2 (BMP-2) on this process was investigated. METHODS: Cartilage explants were single impact loaded, placed within a scaffold and cultured for up to 20 days +/- BMP-2. Cell numbers in the scaffold, on and extruding from the articular surface were quantified and the immunohistochemistry used to identify the cellular phenotype. RESULTS: Following single impact load and culture, chondrocytes were observed in a 3D gelatin scaffold under all culture conditions. Chondrocytes were also observed on the articular surface of the cartilage and extruding out of the parent cartilage and on to the cartilage surface. BMP-2 was demonstrated to quantitatively inhibit these events. CONCLUSION: These studies demonstrate that articular chondrocytes can be stimulated to migrate out of parent cartilage following single impact load and culture. The addition of BMP-2 to the culture medium quantitatively reduced the repair response. It may be that the inhibitory effect of BMP-2 in this experimental model provides a clue to the apparent inability of articular cartilage to heal itself following damage in vivo. BioMed Central 2007-12-05 /pmc/articles/PMC2244625/ /pubmed/18053249 http://dx.doi.org/10.1186/1471-2474-8-120 Text en Copyright © 2007 Henson and Vincent; 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
Henson, Frances MD
Vincent, Thea
Chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair – effect of BMP-2
title Chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair – effect of BMP-2
title_full Chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair – effect of BMP-2
title_fullStr Chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair – effect of BMP-2
title_full_unstemmed Chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair – effect of BMP-2
title_short Chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair – effect of BMP-2
title_sort chondrocyte outgrowth into a gelatin scaffold in a single impact load model of damage/repair – effect of bmp-2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2244625/
https://www.ncbi.nlm.nih.gov/pubmed/18053249
http://dx.doi.org/10.1186/1471-2474-8-120
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