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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...

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Autores principales: Kristensen, Jacob H, Karsdal, Morten A, Sand, Jannie MB, Willumsen, Nicholas, Diefenbach, Claudia, Svensson, Birte, Hägglund, Per, Oersnes-Leeming, Diana J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
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.
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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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