Susceptibility to COPD: differential proteomic profiling after acute smoking.
Cigarette smoking is the main risk factor for COPD (Chronic Obstructive Pulmonary Disease), yet only a subset of smokers develops COPD. Family members of patients with severe early-onset COPD have an increased risk to develop COPD and are therefore defined as "susceptible individuals". Her...
| Main Authors: | , , , , , , , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2014-01-01
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| Series: | PLoS ONE |
| Online Access: | http://europepmc.org/articles/PMC4103835?pdf=render |
| _version_ | 1818478114196422656 |
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| author | Lorenza Franciosi Dirkje S Postma Maarten van den Berge Natalia Govorukhina Peter L Horvatovich Fabrizia Fusetti Bert Poolman Monique E Lodewijk Wim Timens Rainer Bischoff Nick H T ten Hacken |
| author_facet | Lorenza Franciosi Dirkje S Postma Maarten van den Berge Natalia Govorukhina Peter L Horvatovich Fabrizia Fusetti Bert Poolman Monique E Lodewijk Wim Timens Rainer Bischoff Nick H T ten Hacken |
| author_sort | Lorenza Franciosi |
| collection | DOAJ |
| description | Cigarette smoking is the main risk factor for COPD (Chronic Obstructive Pulmonary Disease), yet only a subset of smokers develops COPD. Family members of patients with severe early-onset COPD have an increased risk to develop COPD and are therefore defined as "susceptible individuals". Here we perform unbiased analyses of proteomic profiles to assess how "susceptible individuals" differ from age-matched "non-susceptible individuals" in response to cigarette smoking. Epithelial lining fluid (ELF) was collected at baseline and 24 hours after smoking 3 cigarettes in young individuals susceptible or non-susceptible to develop COPD and older subjects with established COPD. Controls at baseline were older healthy smoking and non-smoking individuals. Five samples per group were pooled and analysed by stable isotope labelling (iTRAQ) in duplicate. Six proteins were selected and validated by ELISA or immunohistochemistry. After smoking, 23 proteins increased or decreased in young susceptible individuals, 7 in young non-susceptible individuals, and 13 in COPD in the first experiment; 23 proteins increased or decreased in young susceptible individuals, 32 in young non-susceptible individuals, and 11 in COPD in the second experiment. SerpinB3 and Uteroglobin decreased after acute smoke exposure in young non-susceptible individuals exclusively, whereas Peroxiredoxin I, S100A9, S100A8, ALDH3A1 (Aldehyde dehydrogenase 3A1) decreased both in young susceptible and non-susceptible individuals, changes being significantly different between groups for Uteroglobin with iTRAQ and for Serpin B3 with iTRAQ and ELISA measures. Peroxiredoxin I, SerpinB3 and ALDH3A1 increased in COPD patients after smoking. We conclude that smoking induces a differential protein response in ELF of susceptible and non-susceptible young individuals, which differs from patients with established COPD. This is the first study applying unbiased proteomic profiling to unravel the underlying mechanisms that induce COPD. Our data suggest that SerpinB3 and Uteroglobin could be interesting proteins in understanding the processes leading to COPD. |
| first_indexed | 2024-12-10T09:44:15Z |
| format | Article |
| id | doaj.art-cf117f202a9d485eb569de2a1a2fcfff |
| institution | Directory Open Access Journal |
| issn | 1932-6203 |
| language | English |
| last_indexed | 2024-12-10T09:44:15Z |
| publishDate | 2014-01-01 |
| publisher | Public Library of Science (PLoS) |
| record_format | Article |
| series | PLoS ONE |
| spelling | doaj.art-cf117f202a9d485eb569de2a1a2fcfff2022-12-22T01:53:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0197e10203710.1371/journal.pone.0102037Susceptibility to COPD: differential proteomic profiling after acute smoking.Lorenza FranciosiDirkje S PostmaMaarten van den BergeNatalia GovorukhinaPeter L HorvatovichFabrizia FusettiBert PoolmanMonique E LodewijkWim TimensRainer BischoffNick H T ten HackenCigarette smoking is the main risk factor for COPD (Chronic Obstructive Pulmonary Disease), yet only a subset of smokers develops COPD. Family members of patients with severe early-onset COPD have an increased risk to develop COPD and are therefore defined as "susceptible individuals". Here we perform unbiased analyses of proteomic profiles to assess how "susceptible individuals" differ from age-matched "non-susceptible individuals" in response to cigarette smoking. Epithelial lining fluid (ELF) was collected at baseline and 24 hours after smoking 3 cigarettes in young individuals susceptible or non-susceptible to develop COPD and older subjects with established COPD. Controls at baseline were older healthy smoking and non-smoking individuals. Five samples per group were pooled and analysed by stable isotope labelling (iTRAQ) in duplicate. Six proteins were selected and validated by ELISA or immunohistochemistry. After smoking, 23 proteins increased or decreased in young susceptible individuals, 7 in young non-susceptible individuals, and 13 in COPD in the first experiment; 23 proteins increased or decreased in young susceptible individuals, 32 in young non-susceptible individuals, and 11 in COPD in the second experiment. SerpinB3 and Uteroglobin decreased after acute smoke exposure in young non-susceptible individuals exclusively, whereas Peroxiredoxin I, S100A9, S100A8, ALDH3A1 (Aldehyde dehydrogenase 3A1) decreased both in young susceptible and non-susceptible individuals, changes being significantly different between groups for Uteroglobin with iTRAQ and for Serpin B3 with iTRAQ and ELISA measures. Peroxiredoxin I, SerpinB3 and ALDH3A1 increased in COPD patients after smoking. We conclude that smoking induces a differential protein response in ELF of susceptible and non-susceptible young individuals, which differs from patients with established COPD. This is the first study applying unbiased proteomic profiling to unravel the underlying mechanisms that induce COPD. Our data suggest that SerpinB3 and Uteroglobin could be interesting proteins in understanding the processes leading to COPD.http://europepmc.org/articles/PMC4103835?pdf=render |
| spellingShingle | Lorenza Franciosi Dirkje S Postma Maarten van den Berge Natalia Govorukhina Peter L Horvatovich Fabrizia Fusetti Bert Poolman Monique E Lodewijk Wim Timens Rainer Bischoff Nick H T ten Hacken Susceptibility to COPD: differential proteomic profiling after acute smoking. PLoS ONE |
| title | Susceptibility to COPD: differential proteomic profiling after acute smoking. |
| title_full | Susceptibility to COPD: differential proteomic profiling after acute smoking. |
| title_fullStr | Susceptibility to COPD: differential proteomic profiling after acute smoking. |
| title_full_unstemmed | Susceptibility to COPD: differential proteomic profiling after acute smoking. |
| title_short | Susceptibility to COPD: differential proteomic profiling after acute smoking. |
| title_sort | susceptibility to copd differential proteomic profiling after acute smoking |
| url | http://europepmc.org/articles/PMC4103835?pdf=render |
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