期刊
RESPIROLOGY
卷 26, 期 10, 页码 960-973出版社
WILEY
DOI: 10.1111/resp.14111
关键词
biomarkers; cigarette smoke; emphysema; experimental chronic obstructive pulmonary disease; mouse model; proteomics; therapeutic targets
资金
- Cancer Council NSW [1099119, 1157073]
- National Health and Medical Research Council [1079187, 1175134, 1137995, 1079184, 1003593, 1179092, 1156589, 1099095]
- University of Technology Sydney
- University of Newcastle
- Australia ECF
- Cancer Institute NSW
- National Health and Medical Research Council of Australia [1179092, 1156589, 1137995, 1099095, 1079184] Funding Source: NHMRC
The study utilized proteomics to uncover major protein changes associated with the pathogenesis and disease progression of COPD, including alterations in RNA biosynthesis, inflammatory responses, mitochondrial function, and oxidative stress. These changes provide insight for developing new effective treatment strategies.
Background and objective Chronic obstructive pulmonary disease (COPD) is the third leading cause of illness and death worldwide. Current treatments aim to control symptoms with none able to reverse disease or stop its progression. We explored the major molecular changes in COPD pathogenesis. Methods We employed quantitative label-based proteomics to map the changes in the lung tissue proteome of cigarette smoke-induced experimental COPD that is induced over 8 weeks and progresses over 12 weeks. Results Quantification of 7324 proteins enabled the tracking of changes to the proteome. Alterations in protein expression profiles occurred in the induction phase, with 18 and 16 protein changes at 4- and 6-week time points, compared to age-matched controls, respectively. Strikingly, 269 proteins had altered expression after 8 weeks when the hallmark pathological features of human COPD emerge, but this dropped to 27 changes at 12 weeks with disease progression. Differentially expressed proteins were validated using other mouse and human COPD bronchial biopsy samples. Major changes in RNA biosynthesis (heterogeneous nuclear ribonucleoproteins C1/C2 [HNRNPC] and RNA-binding protein Musashi homologue 2 [MSI2]) and modulators of inflammatory responses (S100A1) were notable. Mitochondrial dysfunction and changes in oxidative stress proteins also occurred. Conclusion We provide a detailed proteomic profile, identifying proteins associated with the pathogenesis and disease progression of COPD establishing a platform to develop effective new treatment strategies.
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