Effect of age, COPD severity, and cigarette smoke exposure on bronchial epithelial barrier function.

IF 3.5 2区 医学 Q1 PHYSIOLOGY
Kingsley Okechukwu Nwozor, Tillie-Louise Hackett, Qing Chen, Chen Xi Yang, Sheila Patricia Aguilar Lozano, XinZi Zheng, May Al-Fouadi, Tessa M Kole, Alen Faiz, Rashad Mohammad Mahbub, Dirk-Jan Slebos, Karin Klooster, Wim Timens, Maarten van den Berge, Corry-Anke Brandsma, Irene H Heijink
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Abstract

We investigated the effect of age, cigarette smoke, and chronic obstructive pulmonary disease (COPD) severity on epithelial barrier function. Primary bronchial epithelial cells (PBECs) were obtained from bronchial brushings in eight younger and eight older never-smokers; seven older ex-smokers without COPD, eight patients with COPD Global Initiative for Chronic Obstructive Lung Disease (GOLD) I-III and six patients with COPD GOLD IV, and cultured in the absence/presence of cigarette smoke extract (CSE). Epithelial barrier function was assessed by electric resistance sensing and expression of junctional and antioxidant genes/proteins quantified by qPCR/immunodetection. Epithelial barrier function was comparable between PBECs from younger and older never-smokers. PBECs from ex-smokers had significantly lower barrier function compared with never-smokers, with a further decrease in COPD GOLD IV. CSE decreased epithelial barrier function from which PBECs from never-smokers, but not ex-smokers with and without COPD, recovered. Restoration of barrier function was accompanied by increased expression of barrier and antioxidant genes. At baseline, PBECs from ex-smokers with and without COPD had higher expression of junctional and antioxidant genes compared with never-smokers. However, exposure to CSE increased antioxidant (SOD1-3, CAT) gene expression only in PBECs from never-smokers and ex-smokers without COPD. In conclusion, our data indicate that cigarette smoking and COPD severity are associated with reduced epithelial barrier function, which is potentially driven by an imbalance in the antioxidant response.NEW & NOTEWORTHY Cigarette smoking and chronic obstructive pulmonary disease (COPD) severity are associated with reduced epithelial barrier function that is potentially driven by an imbalance in the antioxidant response.

年龄、COPD严重程度和吸烟暴露对支气管上皮屏障功能的影响。
我们研究了年龄、吸烟和慢性阻塞性肺疾病(COPD)严重程度对上皮屏障功能的影响。从8名年轻和8名年长从不吸烟者的支气管刷毛中获得原代支气管上皮细胞(PBECs);7名无COPD的老年前吸烟者,8名COPD全球慢性阻塞性肺疾病倡议(GOLD) I-III型患者和6名COPD GOLD IV型患者,并在没有/存在香烟烟雾提取物(CSE)的情况下进行培养。通过电阻传感和qPCR/免疫检测定量的连接和抗氧化基因/蛋白的表达来评估上皮屏障功能。上皮屏障功能在年轻和年老不吸烟者的PBECs中具有可比性。与不吸烟者相比,戒烟者的PBECs屏障功能明显较低,COPD GOLD IV进一步降低。CSE降低了上皮屏障功能,从不吸烟者的PBECs恢复,但不包括有或没有COPD的戒烟者。屏障功能的恢复伴随着屏障和抗氧化基因的表达增加。在基线时,与不吸烟者相比,伴有和不伴有COPD的戒烟者的PBECs具有更高的连接和抗氧化基因表达。然而,暴露于CSE仅在从不吸烟者和非COPD的戒烟者的PBECs中增加抗氧化剂(SOD1-3, CAT)基因表达。总之,我们的数据表明,吸烟和COPD严重程度与上皮屏障功能降低有关,这可能是由抗氧化反应的不平衡驱动的。吸烟和慢性阻塞性肺疾病(COPD)严重程度与上皮屏障功能降低相关,这可能是由抗氧化反应不平衡驱动的。
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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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