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Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13

INTRODUCTION: Fibronectin fragments have been found in the articular cartilage and synovial fluid of patients with osteoarthritis and rheumatoid arthritis. These matrix fragments can stimulate production of multiple mediators of matrix destruction, including various cytokines and metalloproteinases....

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Autores principales: Long, David, Blake, Simon, Song, Xiao-Yu, Lark, Michael, Loeser, Richard F
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374453/
https://www.ncbi.nlm.nih.gov/pubmed/18289383
http://dx.doi.org/10.1186/ar2376
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author Long, David
Blake, Simon
Song, Xiao-Yu
Lark, Michael
Loeser, Richard F
author_facet Long, David
Blake, Simon
Song, Xiao-Yu
Lark, Michael
Loeser, Richard F
author_sort Long, David
collection PubMed
description INTRODUCTION: Fibronectin fragments have been found in the articular cartilage and synovial fluid of patients with osteoarthritis and rheumatoid arthritis. These matrix fragments can stimulate production of multiple mediators of matrix destruction, including various cytokines and metalloproteinases. The purpose of this study was to discover novel mediators of cartilage destruction using fibronectin fragments as a stimulus. METHODS: Human articular cartilage was obtained from tissue donors and from osteoarthritic cartilage removed at the time of knee replacement surgery. Enzymatically isolated chondrocytes in serum-free cultures were stimulated overnight with the 110 kDa α5β1 integrin-binding fibronectin fragment or with IL-1, IL-6, or IL-7. Cytokines and matrix metalloproteinases released into the media were detected using antibody arrays and quantified by ELISA. IL-7 receptor expression was evaluated by flow cytometry, immunocytochemical staining, and PCR. RESULTS: IL-7 was found to be produced by chondrocytes treated with fibronectin fragments. Compared with cells isolated from normal young adult human articular cartilage, increased IL-7 production was noted in cells isolated from older adult tissue donors and from osteoarthritic cartilage. Chondrocyte IL-7 production was also stimulated by combined treatment with the catabolic cytokines IL-1 and IL-6. Chondrocytes were found to express IL-7 receptors and to respond to IL-7 stimulation with increased production of matrix metalloproteinase-13 and with proteoglycan release from cartilage explants. CONCLUSION: These novel findings indicate that IL-7 may contribute to cartilage destruction in joint diseases, including osteoarthritis.
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spelling pubmed-23744532008-05-09 Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13 Long, David Blake, Simon Song, Xiao-Yu Lark, Michael Loeser, Richard F Arthritis Res Ther Research Article INTRODUCTION: Fibronectin fragments have been found in the articular cartilage and synovial fluid of patients with osteoarthritis and rheumatoid arthritis. These matrix fragments can stimulate production of multiple mediators of matrix destruction, including various cytokines and metalloproteinases. The purpose of this study was to discover novel mediators of cartilage destruction using fibronectin fragments as a stimulus. METHODS: Human articular cartilage was obtained from tissue donors and from osteoarthritic cartilage removed at the time of knee replacement surgery. Enzymatically isolated chondrocytes in serum-free cultures were stimulated overnight with the 110 kDa α5β1 integrin-binding fibronectin fragment or with IL-1, IL-6, or IL-7. Cytokines and matrix metalloproteinases released into the media were detected using antibody arrays and quantified by ELISA. IL-7 receptor expression was evaluated by flow cytometry, immunocytochemical staining, and PCR. RESULTS: IL-7 was found to be produced by chondrocytes treated with fibronectin fragments. Compared with cells isolated from normal young adult human articular cartilage, increased IL-7 production was noted in cells isolated from older adult tissue donors and from osteoarthritic cartilage. Chondrocyte IL-7 production was also stimulated by combined treatment with the catabolic cytokines IL-1 and IL-6. Chondrocytes were found to express IL-7 receptors and to respond to IL-7 stimulation with increased production of matrix metalloproteinase-13 and with proteoglycan release from cartilage explants. CONCLUSION: These novel findings indicate that IL-7 may contribute to cartilage destruction in joint diseases, including osteoarthritis. BioMed Central 2008 2008-02-20 /pmc/articles/PMC2374453/ /pubmed/18289383 http://dx.doi.org/10.1186/ar2376 Text en Copyright © 2008 Long 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
Long, David
Blake, Simon
Song, Xiao-Yu
Lark, Michael
Loeser, Richard F
Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13
title Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13
title_full Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13
title_fullStr Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13
title_full_unstemmed Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13
title_short Human articular chondrocytes produce IL-7 and respond to IL-7 with increased production of matrix metalloproteinase-13
title_sort human articular chondrocytes produce il-7 and respond to il-7 with increased production of matrix metalloproteinase-13
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2374453/
https://www.ncbi.nlm.nih.gov/pubmed/18289383
http://dx.doi.org/10.1186/ar2376
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