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Serological assessment of neutrophil elastase activity on elastin during lung ECM remodeling
BACKGROUND: During the pathological destruction of lung tissue, neutrophil elastase (NE) degrades elastin, one of the major constituents of lung parenchyma. However there are no non-invasive methods to quantify NE degradation of elastin. We selected specific elastin fragments generated by NE for ant...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426538/ https://www.ncbi.nlm.nih.gov/pubmed/25935650 http://dx.doi.org/10.1186/s12890-015-0048-5 |
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author | Kristensen, Jacob H Karsdal, Morten A Sand, Jannie MB Willumsen, Nicholas Diefenbach, Claudia Svensson, Birte Hägglund, Per Oersnes-Leeming, Diana J |
author_facet | Kristensen, Jacob H Karsdal, Morten A Sand, Jannie MB Willumsen, Nicholas Diefenbach, Claudia Svensson, Birte Hägglund, Per Oersnes-Leeming, Diana J |
author_sort | Kristensen, Jacob H |
collection | PubMed |
description | BACKGROUND: During the pathological destruction of lung tissue, neutrophil elastase (NE) degrades elastin, one of the major constituents of lung parenchyma. However there are no non-invasive methods to quantify NE degradation of elastin. We selected specific elastin fragments generated by NE for antibody generation and developed an ELISA assay (EL-NE) for the quantification of NE-degraded elastin. METHODS: Monoclonal antibodies were developed against 10 NE-specific cleavage sites on elastin. One EL-NE assay was tested for analyte stability, linearity and intra- and inter-assay variation. The NE specificity was demonstrated using elastin cleaved in vitro with matrix metalloproteinases (MMPs), cathepsin G (CatG), NE and intact elastin. Clinical relevance was assessed by measuring levels of NE-generated elastin fragments in serum of patients diagnosed with idiopathic pulmonary fibrosis (IPF, n = 10) or lung cancer (n = 40). RESULTS: Analyte recovery of EL-NE for human serum was between 85% and 104%, the analyte was stable for four freeze/thaw cycles and after 24 h storage at 4°C. EL-NE was specific for NE-degraded elastin. Levels of NE-generated elastin fragments for elastin incubated in the presence of NE were 900% to 4700% higher than those seen with CatG or MMP incubation or in intact elastin. Serum levels of NE-generated elastin fragments were significantly increased in patients with IPF (137%, p = 0.002) and in patients with lung cancer (510%, p < 0.001) compared with age- and sex-matched controls. CONCLUSIONS: The EL-NE assay was specific for NE-degraded elastin. The EL-NE assay was able to specifically quantify NE-degraded elastin in serum. Serum levels of NE-degraded elastin might be used to detect excessive lung tissue degradation in lung cancer and IPF. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-015-0048-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4426538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44265382015-05-12 Serological assessment of neutrophil elastase activity on elastin during lung ECM remodeling Kristensen, Jacob H Karsdal, Morten A Sand, Jannie MB Willumsen, Nicholas Diefenbach, Claudia Svensson, Birte Hägglund, Per Oersnes-Leeming, Diana J BMC Pulm Med Research Article BACKGROUND: During the pathological destruction of lung tissue, neutrophil elastase (NE) degrades elastin, one of the major constituents of lung parenchyma. However there are no non-invasive methods to quantify NE degradation of elastin. We selected specific elastin fragments generated by NE for antibody generation and developed an ELISA assay (EL-NE) for the quantification of NE-degraded elastin. METHODS: Monoclonal antibodies were developed against 10 NE-specific cleavage sites on elastin. One EL-NE assay was tested for analyte stability, linearity and intra- and inter-assay variation. The NE specificity was demonstrated using elastin cleaved in vitro with matrix metalloproteinases (MMPs), cathepsin G (CatG), NE and intact elastin. Clinical relevance was assessed by measuring levels of NE-generated elastin fragments in serum of patients diagnosed with idiopathic pulmonary fibrosis (IPF, n = 10) or lung cancer (n = 40). RESULTS: Analyte recovery of EL-NE for human serum was between 85% and 104%, the analyte was stable for four freeze/thaw cycles and after 24 h storage at 4°C. EL-NE was specific for NE-degraded elastin. Levels of NE-generated elastin fragments for elastin incubated in the presence of NE were 900% to 4700% higher than those seen with CatG or MMP incubation or in intact elastin. Serum levels of NE-generated elastin fragments were significantly increased in patients with IPF (137%, p = 0.002) and in patients with lung cancer (510%, p < 0.001) compared with age- and sex-matched controls. CONCLUSIONS: The EL-NE assay was specific for NE-degraded elastin. The EL-NE assay was able to specifically quantify NE-degraded elastin in serum. Serum levels of NE-degraded elastin might be used to detect excessive lung tissue degradation in lung cancer and IPF. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12890-015-0048-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-05-03 /pmc/articles/PMC4426538/ /pubmed/25935650 http://dx.doi.org/10.1186/s12890-015-0048-5 Text en © Kristensen et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), 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 Kristensen, Jacob H Karsdal, Morten A Sand, Jannie MB Willumsen, Nicholas Diefenbach, Claudia Svensson, Birte Hägglund, Per Oersnes-Leeming, Diana J Serological assessment of neutrophil elastase activity on elastin during lung ECM remodeling |
title | Serological assessment of neutrophil elastase activity on elastin during lung ECM remodeling |
title_full | Serological assessment of neutrophil elastase activity on elastin during lung ECM remodeling |
title_fullStr | Serological assessment of neutrophil elastase activity on elastin during lung ECM remodeling |
title_full_unstemmed | Serological assessment of neutrophil elastase activity on elastin during lung ECM remodeling |
title_short | Serological assessment of neutrophil elastase activity on elastin during lung ECM remodeling |
title_sort | serological assessment of neutrophil elastase activity on elastin during lung ecm remodeling |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4426538/ https://www.ncbi.nlm.nih.gov/pubmed/25935650 http://dx.doi.org/10.1186/s12890-015-0048-5 |
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