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The active form of MMP-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases
BACKGROUND: Matrix metalloproteinase-3 (MMP-3) plays an important role in the pathology of rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Measurement of active MMP-3 in clinical samples could provide information about progression of rheumatoid diseases, and potentially response to treatm...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003863/ https://www.ncbi.nlm.nih.gov/pubmed/24641725 http://dx.doi.org/10.1186/1471-2474-15-93 |
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author | Sun, Shu Bay-Jensen, Anne-Christine Karsdal, Morten A Siebuhr, Anne Sofie Zheng, Qinlong Maksymowych, Walter P Christiansen, Thorbjørn G Henriksen, Kim |
author_facet | Sun, Shu Bay-Jensen, Anne-Christine Karsdal, Morten A Siebuhr, Anne Sofie Zheng, Qinlong Maksymowych, Walter P Christiansen, Thorbjørn G Henriksen, Kim |
author_sort | Sun, Shu |
collection | PubMed |
description | BACKGROUND: Matrix metalloproteinase-3 (MMP-3) plays an important role in the pathology of rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Measurement of active MMP-3 in clinical samples could provide information about progression of rheumatoid diseases, and potentially response to treatment. Hence, we aimed to develop a sensitive assay specifically measuring the active form of MMP-3 (act-MMP-3) both in ex vivo models and in human sera. METHODS: A monoclonal antibody against the first 6 amino acids of act-MMP-3 was developed, and the specificity was carefully tested by comparing total and active MMP-3. A technically robust act-MMP-3 ELISA was produced. For biological validation, human synovial membrane and human cartilage explant (HEX) culture models were measured and compared by ELISA and immunoblots. For clinical relevance, the serum levels of act-MMP-3 in AS and RA patients before and after anti-TNF-α treatment were evaluated. RESULTS: A highly specific and technically robust ELISA detecting act-MMP-3 in serum was developed. The lower limit of detection was 33.7 pg/mL. The dilution and spiking recovery of human serum was within 100 ± 20%. The average intra- and inter-assay variations were 3.1% and 13.5% respectively. High levels of act-MMP-3 expression were observed in human synovial membrane culture and oncostatin M and TNF-α stimulated human cartilage. In a cross-sectional study of both AS and RA patients, serum act-MMP-3 level was correlated with C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR). In addition, in patients receiving anti-TNF-α treatment, the serum level of act-MMP-3 was significantly reduced compared to baseline level reflecting the anti-inflammatory effects of the treatment. CONCLUSION: We have successfully developed an assay measuring act-MMP-3 in human serum showing correlation to inflammatory markers. Further studies are required to clarify, whether act-MMP-3 can serve as a predictive marker for outcome in chronic rheumatoid disorders. |
format | Online Article Text |
id | pubmed-4003863 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-40038632014-04-30 The active form of MMP-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases Sun, Shu Bay-Jensen, Anne-Christine Karsdal, Morten A Siebuhr, Anne Sofie Zheng, Qinlong Maksymowych, Walter P Christiansen, Thorbjørn G Henriksen, Kim BMC Musculoskelet Disord Research Article BACKGROUND: Matrix metalloproteinase-3 (MMP-3) plays an important role in the pathology of rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Measurement of active MMP-3 in clinical samples could provide information about progression of rheumatoid diseases, and potentially response to treatment. Hence, we aimed to develop a sensitive assay specifically measuring the active form of MMP-3 (act-MMP-3) both in ex vivo models and in human sera. METHODS: A monoclonal antibody against the first 6 amino acids of act-MMP-3 was developed, and the specificity was carefully tested by comparing total and active MMP-3. A technically robust act-MMP-3 ELISA was produced. For biological validation, human synovial membrane and human cartilage explant (HEX) culture models were measured and compared by ELISA and immunoblots. For clinical relevance, the serum levels of act-MMP-3 in AS and RA patients before and after anti-TNF-α treatment were evaluated. RESULTS: A highly specific and technically robust ELISA detecting act-MMP-3 in serum was developed. The lower limit of detection was 33.7 pg/mL. The dilution and spiking recovery of human serum was within 100 ± 20%. The average intra- and inter-assay variations were 3.1% and 13.5% respectively. High levels of act-MMP-3 expression were observed in human synovial membrane culture and oncostatin M and TNF-α stimulated human cartilage. In a cross-sectional study of both AS and RA patients, serum act-MMP-3 level was correlated with C-reactive protein (CRP) and erythrocyte sedimentation rate (ESR). In addition, in patients receiving anti-TNF-α treatment, the serum level of act-MMP-3 was significantly reduced compared to baseline level reflecting the anti-inflammatory effects of the treatment. CONCLUSION: We have successfully developed an assay measuring act-MMP-3 in human serum showing correlation to inflammatory markers. Further studies are required to clarify, whether act-MMP-3 can serve as a predictive marker for outcome in chronic rheumatoid disorders. BioMed Central 2014-03-19 /pmc/articles/PMC4003863/ /pubmed/24641725 http://dx.doi.org/10.1186/1471-2474-15-93 Text en Copyright © 2014 Sun 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 credited. 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 Sun, Shu Bay-Jensen, Anne-Christine Karsdal, Morten A Siebuhr, Anne Sofie Zheng, Qinlong Maksymowych, Walter P Christiansen, Thorbjørn G Henriksen, Kim The active form of MMP-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases |
title | The active form of MMP-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases |
title_full | The active form of MMP-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases |
title_fullStr | The active form of MMP-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases |
title_full_unstemmed | The active form of MMP-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases |
title_short | The active form of MMP-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases |
title_sort | active form of mmp-3 is a marker of synovial inflammation and cartilage turnover in inflammatory joint diseases |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4003863/ https://www.ncbi.nlm.nih.gov/pubmed/24641725 http://dx.doi.org/10.1186/1471-2474-15-93 |
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