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Advanced glycation endproducts and their receptor in different body compartments in COPD
BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a chronic lung disease characterized by chronic airway inflammation and emphysema, and is caused by exposure to noxious particles or gases, e.g. cigarette smoke. Smoking and oxidative stress lead to accelerated formation and accumulation of...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847335/ https://www.ncbi.nlm.nih.gov/pubmed/27117828 http://dx.doi.org/10.1186/s12931-016-0363-2 |
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author | Hoonhorst, Susan J. M. Lo Tam Loi, Adèle T. Pouwels, Simon D. Faiz, Alen Telenga, Eef D. van den Berge, Maarten Koenderman, Leo Lammers, Jan-Willem J. Boezen, H. Marike van Oosterhout, Antoon J. M. Lodewijk, Monique E. Timens, Wim Postma, Dirkje S. ten Hacken, Nick H. T. |
author_facet | Hoonhorst, Susan J. M. Lo Tam Loi, Adèle T. Pouwels, Simon D. Faiz, Alen Telenga, Eef D. van den Berge, Maarten Koenderman, Leo Lammers, Jan-Willem J. Boezen, H. Marike van Oosterhout, Antoon J. M. Lodewijk, Monique E. Timens, Wim Postma, Dirkje S. ten Hacken, Nick H. T. |
author_sort | Hoonhorst, Susan J. M. |
collection | PubMed |
description | BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a chronic lung disease characterized by chronic airway inflammation and emphysema, and is caused by exposure to noxious particles or gases, e.g. cigarette smoke. Smoking and oxidative stress lead to accelerated formation and accumulation of advanced glycation end products (AGEs), causing local tissue damage either directly or by binding the receptor for AGEs (RAGE). This study assessed the association of AGEs or RAGE in plasma, sputum, bronchial biopsies and skin with COPD and lung function, and their variance between these body compartments. METHODS: Healthy smoking and never-smoking controls (n = 191) and COPD patients (n = 97, GOLD stage I-IV) were included. Autofluorescence (SAF) was measured in the skin, AGEs (pentosidine, CML and CEL) and sRAGE in blood and sputum by ELISA, and in bronchial biopsies by immunohistochemistry. eQTL analysis was performed in bronchial biopsies. RESULTS: COPD patients showed higher SAF values and lower plasma sRAGE levels compared to controls and these values associated with decreased lung function (p <0.001; adjusting for relevant covariates). Lower plasma sRAGE levels significantly and independently predicted higher SAF values (p < 0.001). One SNP (rs2071278) was identified within a region of 50 kB flanking the AGER gene, which was associated with the gene and protein expression levels of AGER and another SNP (rs2071278) which was associated with the accumulation of AGEs in the skin. CONCLUSION: In COPD, AGEs accumulate differentially in body compartments, i.e. they accumulate in the skin, but not in plasma, sputum and bronchial biopsies. The association between lower sRAGE and higher SAF levels supports the hypothesis that the protective mechanism of sRAGE as a decoy-receptor is impaired in COPD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-016-0363-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4847335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48473352016-04-28 Advanced glycation endproducts and their receptor in different body compartments in COPD Hoonhorst, Susan J. M. Lo Tam Loi, Adèle T. Pouwels, Simon D. Faiz, Alen Telenga, Eef D. van den Berge, Maarten Koenderman, Leo Lammers, Jan-Willem J. Boezen, H. Marike van Oosterhout, Antoon J. M. Lodewijk, Monique E. Timens, Wim Postma, Dirkje S. ten Hacken, Nick H. T. Respir Res Research BACKGROUND: Chronic obstructive pulmonary disease (COPD) is a chronic lung disease characterized by chronic airway inflammation and emphysema, and is caused by exposure to noxious particles or gases, e.g. cigarette smoke. Smoking and oxidative stress lead to accelerated formation and accumulation of advanced glycation end products (AGEs), causing local tissue damage either directly or by binding the receptor for AGEs (RAGE). This study assessed the association of AGEs or RAGE in plasma, sputum, bronchial biopsies and skin with COPD and lung function, and their variance between these body compartments. METHODS: Healthy smoking and never-smoking controls (n = 191) and COPD patients (n = 97, GOLD stage I-IV) were included. Autofluorescence (SAF) was measured in the skin, AGEs (pentosidine, CML and CEL) and sRAGE in blood and sputum by ELISA, and in bronchial biopsies by immunohistochemistry. eQTL analysis was performed in bronchial biopsies. RESULTS: COPD patients showed higher SAF values and lower plasma sRAGE levels compared to controls and these values associated with decreased lung function (p <0.001; adjusting for relevant covariates). Lower plasma sRAGE levels significantly and independently predicted higher SAF values (p < 0.001). One SNP (rs2071278) was identified within a region of 50 kB flanking the AGER gene, which was associated with the gene and protein expression levels of AGER and another SNP (rs2071278) which was associated with the accumulation of AGEs in the skin. CONCLUSION: In COPD, AGEs accumulate differentially in body compartments, i.e. they accumulate in the skin, but not in plasma, sputum and bronchial biopsies. The association between lower sRAGE and higher SAF levels supports the hypothesis that the protective mechanism of sRAGE as a decoy-receptor is impaired in COPD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12931-016-0363-2) contains supplementary material, which is available to authorized users. BioMed Central 2016-04-26 2016 /pmc/articles/PMC4847335/ /pubmed/27117828 http://dx.doi.org/10.1186/s12931-016-0363-2 Text en © Hoonhorst et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Hoonhorst, Susan J. M. Lo Tam Loi, Adèle T. Pouwels, Simon D. Faiz, Alen Telenga, Eef D. van den Berge, Maarten Koenderman, Leo Lammers, Jan-Willem J. Boezen, H. Marike van Oosterhout, Antoon J. M. Lodewijk, Monique E. Timens, Wim Postma, Dirkje S. ten Hacken, Nick H. T. Advanced glycation endproducts and their receptor in different body compartments in COPD |
title | Advanced glycation endproducts and their receptor in different body compartments in COPD |
title_full | Advanced glycation endproducts and their receptor in different body compartments in COPD |
title_fullStr | Advanced glycation endproducts and their receptor in different body compartments in COPD |
title_full_unstemmed | Advanced glycation endproducts and their receptor in different body compartments in COPD |
title_short | Advanced glycation endproducts and their receptor in different body compartments in COPD |
title_sort | advanced glycation endproducts and their receptor in different body compartments in copd |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4847335/ https://www.ncbi.nlm.nih.gov/pubmed/27117828 http://dx.doi.org/10.1186/s12931-016-0363-2 |
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