Department of Inflammation and Immunity, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio, United States.
Enterprise Respiratory Care Research Cleveland Clinic, Cleveland Clinic Children's, Cleveland, Ohio, United States.
Am J Physiol Lung Cell Mol Physiol. 2023 Nov 1;325(5):L580-L593. doi: 10.1152/ajplung.00135.2023. Epub 2023 Sep 12.
The use of electronic cigarettes (e-cigs), especially among teenagers, has reached alarming and epidemic levels, posing a significant threat to public health. However, the short- and long-term effects of vaping on the airway epithelial barrier are unclear. Airway epithelial cells are the forefront protectors from viruses and pathogens. They contain apical junctional complexes (AJCs), which include tight junctions (TJs) and adherens junctions (AJs) formed between adjacent cells. Previously, we reported respiratory syncytial virus (RSV) infection, the leading cause of acute lower respiratory infection-related hospitalization in children and high-risk adults, induces a "leaky airway" by disrupting the epithelial AJC structure and function. We hypothesized chemical components of e-cigs disrupt airway epithelial barrier and exacerbate RSV-induced airway barrier dysfunction. Using confluent human bronchial epithelial (16HBE) cells and well-differentiated normal human bronchial epithelial (NHBE) cells, we found that exposure to extract and aerosol e-cig nicotine caused a significant decrease in transepithelial electrical resistance (TEER) and the structure of the AJC even at noncytotoxic concentrations. Western blot analysis of 16HBE cells exposed to e-cig nicotine extract did not reveal significant changes in AJC proteins. Exposure to aerosolized e-cig cinnamon or menthol flavors also induced barrier disruption and aggravated nicotine-induced airway barrier dysfunction. Moreover, preexposure to nicotine aerosol increased RSV infection and the severity of RSV-induced airway barrier disruption. Our findings demonstrate that e-cig exposure disrupts the airway epithelial barrier and exacerbates RSV-induced damage. Knowledge gained from this study will provide awareness of adverse e-cig respiratory effects and positively impact the mitigation of e-cig epidemic. Electronic cigarette (e-cig) use, especially in teens, is alarming and at epidemic proportions, threatening public health. Our study shows that e-cig nicotine exposure disrupts airway epithelial tight junctions and increases RSV-induced barrier dysfunction. Furthermore, exposure to aerosolized flavors exaggerates e-cig nicotine-induced airway barrier dysfunction. Our study confirms that individual and combined components of e-cigs deleteriously impact the airway barrier and that e-cig exposure increases susceptibility to viral infection.
电子烟(e-cigs)的使用,尤其是在青少年中的使用,已经达到了惊人的、流行的程度,对公共健康构成了重大威胁。然而,蒸气对气道上皮屏障的短期和长期影响尚不清楚。气道上皮细胞是抵御病毒和病原体的第一道防线。它们包含顶端连接复合体(AJCs),包括紧密连接(TJs)和相邻细胞之间形成的黏着连接(AJs)。此前,我们报道呼吸道合胞病毒(RSV)感染,是导致儿童和高危成人急性下呼吸道感染相关住院的主要原因,通过破坏上皮 AJC 的结构和功能导致“气道渗漏”。我们假设电子烟的化学物质成分破坏气道上皮屏障,并使 RSV 诱导的气道屏障功能障碍恶化。我们使用贴壁的人支气管上皮(16HBE)细胞和分化良好的正常人支气管上皮(NHBE)细胞,发现即使在非细胞毒性浓度下,暴露于电子烟尼古丁提取物和雾化电子烟尼古丁也会导致跨上皮电阻(TEER)和 AJC 结构显著降低。对暴露于电子烟尼古丁提取物的 16HBE 细胞进行的 Western blot 分析并未显示 AJC 蛋白有明显变化。暴露于雾化电子烟肉桂或薄荷风味也会引起屏障破坏,并加重尼古丁诱导的气道屏障功能障碍。此外,预先暴露于尼古丁雾化会增加 RSV 感染和 RSV 诱导的气道屏障破坏的严重程度。我们的研究结果表明,电子烟暴露会破坏气道上皮屏障,并加重 RSV 诱导的损伤。从这项研究中获得的知识将提高对电子烟呼吸不良影响的认识,并积极影响电子烟流行的缓解。电子烟(e-cigs)的使用,尤其是在青少年中,令人震惊且呈流行趋势,对公共健康构成威胁。我们的研究表明,电子烟尼古丁暴露会破坏气道上皮紧密连接,并增加 RSV 引起的屏障功能障碍。此外,暴露于雾化风味会加剧电子烟尼古丁引起的气道屏障功能障碍。我们的研究证实,电子烟的个体和组合成分对气道屏障有害,电子烟暴露会增加对病毒感染的易感性。