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Cartilage oligomeric matrix protein deficiency promotes early onset and the chronic development of collagen-induced arthritis
INTRODUCTION: Cartilage oligomeric matrix protein (COMP) is a homopentameric protein in cartilage. The development of arthritis, like collagen-induced arthritis (CIA), involves cartilage as a target tissue. We have investigated the development of CIA in COMP-deficient mice. METHODS: COMP-deficient m...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656236/ https://www.ncbi.nlm.nih.gov/pubmed/19014566 http://dx.doi.org/10.1186/ar2551 |
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author | Geng, Hui Carlsen, Stefan Nandakumar, Kutty Selva Holmdahl, Rikard Aspberg, Anders Oldberg, Åke Mattsson, Ragnar |
author_facet | Geng, Hui Carlsen, Stefan Nandakumar, Kutty Selva Holmdahl, Rikard Aspberg, Anders Oldberg, Åke Mattsson, Ragnar |
author_sort | Geng, Hui |
collection | PubMed |
description | INTRODUCTION: Cartilage oligomeric matrix protein (COMP) is a homopentameric protein in cartilage. The development of arthritis, like collagen-induced arthritis (CIA), involves cartilage as a target tissue. We have investigated the development of CIA in COMP-deficient mice. METHODS: COMP-deficient mice in the 129/Sv background were backcrossed for 10 generations against B10.Q mice, which are susceptible to chronic CIA. COMP-deficient and wild-type mice were tested for onset, incidence, and severity of arthritis in both the collagen and collagen antibody-induced arthritis models. Serum anti-collagen II and anti-COMP antibodies as well as serum COMP levels in arthritic and wild-type mice were measured by enzyme-linked immunosorbent assay. RESULTS: COMP-deficient mice showed a significant early onset and increase in the severity of CIA in the chronic phase, whereas collagen II-antibody titers were similar in COMP-deficient and wild-type controls. COMP antibodies were not found in wild-type mice. Finally, COMP-deficient and wild-type mice responded similarly to collagen antibody-induced arthritis, indicating no difference in how collagen II antibodies interact with COMP-deficient cartilage during the initial stages of arthritis. CONCLUSIONS: COMP deficiency enhances the early onset and development of chronic arthritis but does not affect collagen II autoimmunity. These findings accentuate the importance of COMP in cartilage stability. |
format | Text |
id | pubmed-2656236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26562362009-03-17 Cartilage oligomeric matrix protein deficiency promotes early onset and the chronic development of collagen-induced arthritis Geng, Hui Carlsen, Stefan Nandakumar, Kutty Selva Holmdahl, Rikard Aspberg, Anders Oldberg, Åke Mattsson, Ragnar Arthritis Res Ther Research Article INTRODUCTION: Cartilage oligomeric matrix protein (COMP) is a homopentameric protein in cartilage. The development of arthritis, like collagen-induced arthritis (CIA), involves cartilage as a target tissue. We have investigated the development of CIA in COMP-deficient mice. METHODS: COMP-deficient mice in the 129/Sv background were backcrossed for 10 generations against B10.Q mice, which are susceptible to chronic CIA. COMP-deficient and wild-type mice were tested for onset, incidence, and severity of arthritis in both the collagen and collagen antibody-induced arthritis models. Serum anti-collagen II and anti-COMP antibodies as well as serum COMP levels in arthritic and wild-type mice were measured by enzyme-linked immunosorbent assay. RESULTS: COMP-deficient mice showed a significant early onset and increase in the severity of CIA in the chronic phase, whereas collagen II-antibody titers were similar in COMP-deficient and wild-type controls. COMP antibodies were not found in wild-type mice. Finally, COMP-deficient and wild-type mice responded similarly to collagen antibody-induced arthritis, indicating no difference in how collagen II antibodies interact with COMP-deficient cartilage during the initial stages of arthritis. CONCLUSIONS: COMP deficiency enhances the early onset and development of chronic arthritis but does not affect collagen II autoimmunity. These findings accentuate the importance of COMP in cartilage stability. BioMed Central 2008 2008-11-14 /pmc/articles/PMC2656236/ /pubmed/19014566 http://dx.doi.org/10.1186/ar2551 Text en Copyright © 2008 Geng 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 Geng, Hui Carlsen, Stefan Nandakumar, Kutty Selva Holmdahl, Rikard Aspberg, Anders Oldberg, Åke Mattsson, Ragnar Cartilage oligomeric matrix protein deficiency promotes early onset and the chronic development of collagen-induced arthritis |
title | Cartilage oligomeric matrix protein deficiency promotes early onset and the chronic development of collagen-induced arthritis |
title_full | Cartilage oligomeric matrix protein deficiency promotes early onset and the chronic development of collagen-induced arthritis |
title_fullStr | Cartilage oligomeric matrix protein deficiency promotes early onset and the chronic development of collagen-induced arthritis |
title_full_unstemmed | Cartilage oligomeric matrix protein deficiency promotes early onset and the chronic development of collagen-induced arthritis |
title_short | Cartilage oligomeric matrix protein deficiency promotes early onset and the chronic development of collagen-induced arthritis |
title_sort | cartilage oligomeric matrix protein deficiency promotes early onset and the chronic development of collagen-induced arthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656236/ https://www.ncbi.nlm.nih.gov/pubmed/19014566 http://dx.doi.org/10.1186/ar2551 |
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