电子烟对临床前小鼠气道上皮屏障完整性的影响。

IF 3.5 2区 医学 Q1 PHYSIOLOGY
Amelia L Beaumont, Andjela Raduka, Nannan Gao, Claire E Lee, Robert L Chatburn, Fariba Rezaee
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引用次数: 0

摘要

青少年中越来越多地使用电子烟(e-cigs)构成了重大的公共健康风险。本研究探讨了电子烟对气道上皮屏障的影响,重点研究了尖端连接复合物(AJCs),包括紧密连接(TJs)和粘附连接(AJs)。我们假设电子烟在小鼠模型中破坏AJCs,导致气道屏障通透性增加。C57BL/6小鼠暴露于36 mg/mL的电子烟气溶胶(每分钟3支),每天1小时,持续4天。采用支气管肺泡灌洗(BAL)液分析、肺炎症评估、免疫组化(IHC)染色、Western blotting (WB)和通透性分析评估气道屏障的结构和功能。暴露于电子烟的小鼠体重减轻,血清可替宁水平升高。BAL液分析显示白细胞升高。组织学分析证实肺部炎症,而免疫组化和WB显示明显的AJC破坏。值得注意的是,与对照组相比,接触电子烟的小鼠的claudin-2水平升高。众所周知,Claudin-2在促进“渗漏”上皮的通透性中起作用,它随着其他TJ成分的减少而增加,表明结构屏障受损。电子烟暴露后,气道内灌注fitc -葡聚糖升高血清fitc -葡聚糖水平,表明屏障通透性增强。电子烟气溶胶暴露会破坏气道上皮屏障的结构和功能,主要是通过破坏tj和AJs。这些发现为进一步研究电子烟的健康风险提供了潜在的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The impact of electronic cigarettes on airway epithelial barrier integrity in preclinical mouse model.

The increasing use of electronic cigarettes (e-cigs) among adolescents poses significant public health risks. This study investigates the impact of e-cigs on the airway epithelial barrier, focusing on apical junctional complexes (AJCs), including tight junctions (TJs) and adherens junctions (AJs). We hypothesized that e-cigs disrupt AJCs in a mouse model, leading to increased airway barrier permeability. C57BL/6 mice were exposed to 36 mg/mL e-cig aerosols (3 puffs/min) for 1 h daily over 4 days. Bronchoalveolar lavage (BAL) fluid analysis, lung inflammation assessment, immunohistochemistry (IHC) staining, Western blotting (WB), and permeability assays were performed to evaluate the structure and function of the airway barrier. E-cig-exposed mice showed weight loss and elevated serum cotinine levels. BAL fluid analysis revealed elevated white blood cells. Histological analysis confirmed lung inflammation, whereas IHC and WB showed significant AJC disruption. Notably, claudin-2 levels were elevated in e-cig-exposed mice compared with controls. Claudin-2, known for its role in promoting permeability in "leaky" epithelia, increased alongside decreases in other TJ components, signifying structural barrier impairment. After e-cig exposure, instilling fluorescein isothiocyanate (FITC)-dextran into the airway increased serum FITC-dextran levels, indicating enhanced barrier permeability. E-cig aerosol exposure disrupts airway epithelial barrier structure and function, primarily through the disassembly of TJs and AJs. These findings suggest potential pathways for further clinical investigation into the health risks of e-cig use.NEW & NOTEWORTHY The rising use of e-cigs among youth has become a significant public health concern. This study, using a mouse model, demonstrates that exposure to e-cig aerosol leads to airway inflammation, structural damage to the airway epithelial barrier, and increased epithelial barrier permeability.

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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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