Altered Extracellular Vesicle-Derived Protein and microRNA Signatures in Bronchoalveolar Lavage Fluid from Patients with Chronic Obstructive Pulmonary Disease

被引:0
|
作者
Bartel, Sabine [1 ,2 ]
Wolters, Justina C. [3 ]
Noor, Hasnat [1 ,2 ]
Rafie, Karim [4 ]
Fang, Jiahua [1 ,2 ]
Kirchner, Benedikt [5 ,6 ]
Nolte-'t Hoen, Esther [7 ]
Pfaffl, Michael W. [5 ]
Rutgers, Steven [8 ]
Timens, Wim [1 ,2 ]
van den Berge, Maarten [2 ,9 ]
Hylkema, Machteld N. [1 ,2 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Pathol & Med Biol, NL-9713 GZ Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Groningen Res Inst Asthma & COPD GRIAC, NL-9713 GZ Groningen, Netherlands
[3] Univ Groningen, Univ Med Ctr Groningen, Dept Pediat, NL-9713 GZ Groningen, Netherlands
[4] Univ Groningen, Groningen Res Inst Pharm GRIP, Dept Mol Pharmacol, NL-9712 CP Groningen, Netherlands
[5] Tech Univ Munich, Sch Life Sci Weihenstephan, Div Anim Physiol & Immunol, D-85354 Freising Weihenstephan, Germany
[6] Ludwig Maximilians Univ Munchen, LMU Univ Hosp, Inst Human Genet, D-80539 Munich, Germany
[7] Univ Utrecht, Fac Vet Med, Dept Biomol Hlth Sci, NL-3584 CS Utrecht, Netherlands
[8] Scheper Hosp, NL-7824 AA Emmen, Netherlands
[9] Univ Groningen, Univ Med Ctr Groningen, Dept Pulm Dis, NL-9713 GZ Groningen, Netherlands
关键词
chronic obstructive pulmonary disease (COPD); extracellular vesicle (EV); proteomics; miRNA; bronchoalveolar lavage (BAL); inflammation; COPD; LACTOFERRIN; LYSOZYME; EXOSOMES; SPUTUM;
D O I
10.3390/cells13110945
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chronic obstructive pulmonary disease (COPD) is a progressive lung disease for which there is no cure. Accumulating research results suggest a role for extracellular vesicles (EVs) in the pathogenesis of COPD. This study aimed to uncover the involvement of EVs and their molecular cargo in the progression of COPD by identification of EV-associated protein and microRNA (miRNA) profiles. We isolated EVs from the bronchial alveolar lavage fluid (BALF) of 18 patients with COPD and 11 healthy controls using size-exclusion chromatography. EV isolates were characterized using nanoparticle tracking analysis and protein content. Proteomic analysis revealed a higher abundance of 284 proteins (log2FC > 1) and a lower abundance of 3 proteins (log2FC < -1) in EVs derived from patients with COPD. Ingenuity pathway analysis showed that proteins enriched in COPD-associated EVs trigger inflammatory responses, including neutrophil degranulation. Variances in surface receptors and ligands associated with COPD EVs suggest a preferential interaction with alveolar cells. Small RNAseq analysis identified a higher abundance of ten miRNAs and a lower abundance of one miRNA in EVs from COPD versus controls (Basemean > 100, FDR < 0.05). Our data indicate that the molecular composition of EVs in the BALF of patients with COPD is altered compared to healthy control EVs. Several components in COPD EVs were identified that may perpetuate inflammation and alveolar tissue destruction.
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页数:21
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