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Expression of calgranulin A/B heterodimer after acute inhalation of endotoxin: proteomic approach and validation
BACKGROUND: The acute inhalation of endotoxin mimicks several aspects of the inflammation related to chronic obstructive pulmonary disease (COPD). The aim of the current study was to identify and to validate biomarkers of endotoxin-induced airways’ inflammation. METHODS: The cellular count in the in...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225611/ https://www.ncbi.nlm.nih.gov/pubmed/24237763 http://dx.doi.org/10.1186/1471-2466-13-65 |
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author | Michel, Olivier Doyen, Virginie Leroy, Baptiste Bopp, Benjamin Dinh, Duc Huy Phong Corazza, Francis Wattiez, Ruddy |
author_facet | Michel, Olivier Doyen, Virginie Leroy, Baptiste Bopp, Benjamin Dinh, Duc Huy Phong Corazza, Francis Wattiez, Ruddy |
author_sort | Michel, Olivier |
collection | PubMed |
description | BACKGROUND: The acute inhalation of endotoxin mimicks several aspects of the inflammation related to chronic obstructive pulmonary disease (COPD). The aim of the current study was to identify and to validate biomarkers of endotoxin-induced airways’ inflammation. METHODS: The cellular count in the induced-sputum, was measured before and after an inhalation of 20 mcg endotoxin, in 8 healthy volunteers. A proteomic analysis was applied to identify the more relevant proteins expression, before measurement by ELISA. The amplitude and the repeatability of the markers were evaluated among another population of 12 healthy subjects. RESULTS: There was a significant rise of viable cells (p <0.01), macrophages (p <0.05), and neutrophils (p <0.02) 24 hours after endotoxin inhalation, and of neutrophils (p <0.02) and lymphocytes (p <0.05) at 6 hours. Among the highest amplitude responses, the two dimensional electrophoretic separation shown proteolytic activity and overexpression of protein spots. By MALDI-TOF mass spectrometry, the last were identified as calgranulin A and B. The expression of the bioactive A/B heterodimeric complex was confirmed by ELISA both in the sputum (p <0.01) and at the blood level (p <0.01). The intra-subject repeatability of the sputum calgranulin A/B was highly significant (p <0.0001). CONCLUSION: In healthy subjects, the inhalation of endotoxin induced expression of sputum calgranulin A/B that could be a biomarker of the endotoxin response/exposure. |
format | Online Article Text |
id | pubmed-4225611 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42256112014-11-11 Expression of calgranulin A/B heterodimer after acute inhalation of endotoxin: proteomic approach and validation Michel, Olivier Doyen, Virginie Leroy, Baptiste Bopp, Benjamin Dinh, Duc Huy Phong Corazza, Francis Wattiez, Ruddy BMC Pulm Med Research Article BACKGROUND: The acute inhalation of endotoxin mimicks several aspects of the inflammation related to chronic obstructive pulmonary disease (COPD). The aim of the current study was to identify and to validate biomarkers of endotoxin-induced airways’ inflammation. METHODS: The cellular count in the induced-sputum, was measured before and after an inhalation of 20 mcg endotoxin, in 8 healthy volunteers. A proteomic analysis was applied to identify the more relevant proteins expression, before measurement by ELISA. The amplitude and the repeatability of the markers were evaluated among another population of 12 healthy subjects. RESULTS: There was a significant rise of viable cells (p <0.01), macrophages (p <0.05), and neutrophils (p <0.02) 24 hours after endotoxin inhalation, and of neutrophils (p <0.02) and lymphocytes (p <0.05) at 6 hours. Among the highest amplitude responses, the two dimensional electrophoretic separation shown proteolytic activity and overexpression of protein spots. By MALDI-TOF mass spectrometry, the last were identified as calgranulin A and B. The expression of the bioactive A/B heterodimeric complex was confirmed by ELISA both in the sputum (p <0.01) and at the blood level (p <0.01). The intra-subject repeatability of the sputum calgranulin A/B was highly significant (p <0.0001). CONCLUSION: In healthy subjects, the inhalation of endotoxin induced expression of sputum calgranulin A/B that could be a biomarker of the endotoxin response/exposure. BioMed Central 2013-11-15 /pmc/articles/PMC4225611/ /pubmed/24237763 http://dx.doi.org/10.1186/1471-2466-13-65 Text en Copyright © 2013 Michel 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 Michel, Olivier Doyen, Virginie Leroy, Baptiste Bopp, Benjamin Dinh, Duc Huy Phong Corazza, Francis Wattiez, Ruddy Expression of calgranulin A/B heterodimer after acute inhalation of endotoxin: proteomic approach and validation |
title | Expression of calgranulin A/B heterodimer after acute inhalation of endotoxin: proteomic approach and validation |
title_full | Expression of calgranulin A/B heterodimer after acute inhalation of endotoxin: proteomic approach and validation |
title_fullStr | Expression of calgranulin A/B heterodimer after acute inhalation of endotoxin: proteomic approach and validation |
title_full_unstemmed | Expression of calgranulin A/B heterodimer after acute inhalation of endotoxin: proteomic approach and validation |
title_short | Expression of calgranulin A/B heterodimer after acute inhalation of endotoxin: proteomic approach and validation |
title_sort | expression of calgranulin a/b heterodimer after acute inhalation of endotoxin: proteomic approach and validation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4225611/ https://www.ncbi.nlm.nih.gov/pubmed/24237763 http://dx.doi.org/10.1186/1471-2466-13-65 |
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