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Articular cartilage gene expression patterns in the tissue surrounding the impact site following applications of shear and axial loads

ABSTRACT: BACKGROUND: Osteoarthritis is a degradative joint disease found in humans and commercial swine which can develop from a number of factors, including prior joint trauma. An impact injury model was developed to deliver in vitro loads to disease-free porcine patellae in a model of OA. METHODS...

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Autores principales: McCulloch, R. S., Mente, P. L., O’Nan, A. T., Ashwell, M. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303924/
https://www.ncbi.nlm.nih.gov/pubmed/30579353
http://dx.doi.org/10.1186/s12891-018-2374-2
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author McCulloch, R. S.
Mente, P. L.
O’Nan, A. T.
Ashwell, M. S.
author_facet McCulloch, R. S.
Mente, P. L.
O’Nan, A. T.
Ashwell, M. S.
author_sort McCulloch, R. S.
collection PubMed
description ABSTRACT: BACKGROUND: Osteoarthritis is a degradative joint disease found in humans and commercial swine which can develop from a number of factors, including prior joint trauma. An impact injury model was developed to deliver in vitro loads to disease-free porcine patellae in a model of OA. METHODS: Axial impactions (2000 N normal) and shear impactions (500 N normal with induced shear forces) were delivered to 48 randomly assigned patellae. The patellae were then cultured for 0, 3, 7, or 14 days following the impact. Specimens in the tissue surrounding the loading site were harvested and expression of 18 OA related genes was studied via quantitative PCR. The selected genes were previously identified from published work and fell into four categories: cartilage matrix, degradative enzymes, inflammatory response, and apoptosis. RESULTS: Type II collagen (Col2a1) showed significantly lower expression in shear vs. axial adjacent tissue at day 0 and 7 (fold changes of 0.40 & 0.19, respectively). In addition, higher expression of degradative enzymes and Fas, an apoptosis gene, was observed in the shear specimens. CONCLUSIONS: The results suggest that a more physiologically valid shear load may induce more damage to surrounding articular cartilage than a normal load alone. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12891-018-2374-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-63039242018-12-31 Articular cartilage gene expression patterns in the tissue surrounding the impact site following applications of shear and axial loads McCulloch, R. S. Mente, P. L. O’Nan, A. T. Ashwell, M. S. BMC Musculoskelet Disord Research Article ABSTRACT: BACKGROUND: Osteoarthritis is a degradative joint disease found in humans and commercial swine which can develop from a number of factors, including prior joint trauma. An impact injury model was developed to deliver in vitro loads to disease-free porcine patellae in a model of OA. METHODS: Axial impactions (2000 N normal) and shear impactions (500 N normal with induced shear forces) were delivered to 48 randomly assigned patellae. The patellae were then cultured for 0, 3, 7, or 14 days following the impact. Specimens in the tissue surrounding the loading site were harvested and expression of 18 OA related genes was studied via quantitative PCR. The selected genes were previously identified from published work and fell into four categories: cartilage matrix, degradative enzymes, inflammatory response, and apoptosis. RESULTS: Type II collagen (Col2a1) showed significantly lower expression in shear vs. axial adjacent tissue at day 0 and 7 (fold changes of 0.40 & 0.19, respectively). In addition, higher expression of degradative enzymes and Fas, an apoptosis gene, was observed in the shear specimens. CONCLUSIONS: The results suggest that a more physiologically valid shear load may induce more damage to surrounding articular cartilage than a normal load alone. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12891-018-2374-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-22 /pmc/articles/PMC6303924/ /pubmed/30579353 http://dx.doi.org/10.1186/s12891-018-2374-2 Text en © The Author(s). 2018 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
McCulloch, R. S.
Mente, P. L.
O’Nan, A. T.
Ashwell, M. S.
Articular cartilage gene expression patterns in the tissue surrounding the impact site following applications of shear and axial loads
title Articular cartilage gene expression patterns in the tissue surrounding the impact site following applications of shear and axial loads
title_full Articular cartilage gene expression patterns in the tissue surrounding the impact site following applications of shear and axial loads
title_fullStr Articular cartilage gene expression patterns in the tissue surrounding the impact site following applications of shear and axial loads
title_full_unstemmed Articular cartilage gene expression patterns in the tissue surrounding the impact site following applications of shear and axial loads
title_short Articular cartilage gene expression patterns in the tissue surrounding the impact site following applications of shear and axial loads
title_sort articular cartilage gene expression patterns in the tissue surrounding the impact site following applications of shear and axial loads
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303924/
https://www.ncbi.nlm.nih.gov/pubmed/30579353
http://dx.doi.org/10.1186/s12891-018-2374-2
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