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Long-term smoking alters abundance of over half of the proteome in bronchoalveolar lavage cell in smokers with normal spirometry, with effects on molecular pathways associated with COPD

机译:长期吸烟会改变肺活量正常的吸烟者支气管肺泡灌洗细胞中一半以上蛋白质组的丰度,并影响与COPD相关的分子途径

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BackgroundSmoking represents a significant risk factor for many chronic inflammatory diseases, including chronic obstructive pulmonary disease (COPD). MethodsTo identify dysregulation of specific proteins and pathways in bronchoalveolar lavage (BAL) cells associated with smoking, isobaric tags for relative and absolute quantitation (iTRAQ)-based shotgun proteomics analyses were performed on BAL cells from healthy never-smokers and smokers with normal lung function from the Karolinska COSMIC cohort. Multivariate statistical modeling, multivariate correlations with clinical data, and pathway enrichment analysis were performed. ResultsSmoking exerted a significant impact on the BAL cell proteome, with more than 500 proteins representing 15 molecular pathways altered due to smoking. The majority of these alterations occurred in a gender-independent manner. The phagosomal- and leukocyte trans endothelial migration (LTM) pathways significantly correlated with FEV1/FVC as well as the percentage of CD8+ T-cells and CD8+CD69+ T-cells in smokers. The correlations to clinical parameters in healthy never-smokers were minor. ConclusionThe significant correlations of proteins in the phagosome- and LTM pathways with activated cytotoxic T-cells (CD69+) and the level of airway obstruction (FEV1/FVC) in smokers, both hallmarks of COPD, suggests that these two pathways may play a role in the molecular events preceding the development of COPD in susceptible smokers. Both pathways were found to be further dysregulated in COPD patients from the same cohort, thereby providing further support to this hypothesis. Given that not all smokers develop COPD in spite of decades of smoking, it is also plausible that some of the molecular pathways associated with response to smoking exert protective mechanisms to smoking-related pathologies in resilient individuals. Trial registration ClinicalTrials.gov identifier NCT02627872 ; Retrospectively registered on December 9, 2015.
机译:背景技术吸烟是许多慢性炎性疾病(包括慢性阻塞性肺疾病(COPD))的重要危险因素。方法为了确定与吸烟有关的支气管肺泡灌洗(BAL)细胞中特定蛋白质的失调和途径,对来自健康,从未吸烟者和肺功能正常的吸烟者的BAL细胞进行了基于等压和绝对定量(iTRAQ)的)弹蛋白质组学分析来自Karolinska COSMIC队列。进行了多元统计建模,与临床数据的多元相关性以及途径富集分析。结果吸烟对BAL细胞蛋白质组产生了重大影响,由于吸烟,改变了代表15种分子途径的500多种蛋白质。这些改变中的大多数以与性别无关的方式发生。吞噬体和白细胞跨内皮迁移(LTM)途径与FEV 1 / FVC以及CD8 + T细胞和CD8 +的百分比显着相关吸烟者 CD69 + T细胞。健康的不吸烟者与临床参数的相关性很小。结论吸烟者吞噬体和LTM途径中的蛋白质与激活的细胞毒性T细胞(CD69 +)和气道阻塞水平(FEV 1 / FVC)呈显着相关性,这两者均为COPD的标志。这两个途径可能在易感吸烟者发生COPD之前的分子事件中起作用。在同一队列的COPD患者中发现这两种途径均进一步失调,从而进一步支持了这一假设。考虑到尽管吸烟数十年,并非所有吸烟者都会发展为COPD,所以与吸烟反应相关的某些分子途径对具有弹性的个体中与吸烟相关的病理表现出保护性机制也是合理的。试验注册ClinicalTrials.gov标识符NCT02627872;追溯注册于2015年12月9日。

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