Susceptibility to COPD
| Autor: | Rainer Bischoff, Maarten van den Berge, Natalia Govorukhina, Fabrizia Fusetti, Peter Horvatovich, Wim Timens, Berend Poolman, Monique E. Lodewijk, Dirkje S. Postma, Lorenza Franciosi, Nicolaas ten Hacken |
|---|---|
| Přispěvatelé: | Analytical Biochemistry, Groningen Research Institute for Asthma and COPD (GRIAC), Medicinal Chemistry and Bioanalysis (MCB), Enzymology, Lifestyle Medicine (LM), Guided Treatment in Optimal Selected Cancer Patients (GUTS) |
| Jazyk: | angličtina |
| Rok vydání: | 2014 |
| Předmět: |
Proteomics
Male Time Factors Pulmonology PROTEIN EXPRESSION lcsh:Medicine Drug Addiction Biochemistry Epithelium Recreational Drug Addiction Pulmonary Disease Chronic Obstructive Medicine and Health Sciences Psychology Young adult OXIDATIVE STRESS lcsh:Science COPD Multidisciplinary medicine.diagnostic_test biology Immunochemistry Smoking Middle Aged medicine.anatomical_structure Female Disease Susceptibility Research Article Adult Adolescent Chronic Obstructive Pulmonary Disease Immunology BIOMARKERS Addiction OBSTRUCTIVE PULMONARY-DISEASE BRONCHOALVEOLAR LAVAGE S100A8 Young Adult medicine Humans Risk factor SPUTUM PROTEOMICS Lung business.industry Proteomic Profiling lcsh:R Biology and Life Sciences Proteins MASS-SPECTROMETRY medicine.disease respiratory tract diseases Bronchoalveolar lavage CIGARETTE-SMOKE Uteroglobin biology.protein EPITHELIAL LINING FLUID lcsh:Q business LUNG |
| Zdroj: | PLoS ONE PLoS ONE, Vol 9, Iss 7, p e102037 (2014) PLoS ONE, 9(7):e102037. PUBLIC LIBRARY SCIENCE |
| ISSN: | 1932-6203 |
| Popis: | 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. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|