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电子烟烟雾具有细胞毒性并增加人呼吸道上皮细胞上的ACE2表达:对严重急性呼吸综合征冠状病毒2(COVID-19)的影响

Electronic Cigarette Aerosol Is Cytotoxic and Increases ACE2 Expression on Human Airway Epithelial Cells: Implications for SARS-CoV-2 (COVID-19).

作者信息

McAlinden Kielan Darcy, Lu Wenying, Ferdowsi Parisa Vahidi, Myers Stephen, Markos James, Larby Josie, Chia Collin, Weber Heinrich C, Haug Greg, Eapen Mathew Suji, Sohal Sukhwinder Singh

机构信息

Respiratory Translational Research Group, Department of Laboratory Medicine, School of Health Sciences, College of Health and Medicine, University of Tasmania, Launceston, Tasmania 7248, Australia.

Department of Respiratory Medicine, Launceston General Hospital, Launceston, Tasmania 7250, Australia.

出版信息

J Clin Med. 2021 Mar 3;10(5):1028. doi: 10.3390/jcm10051028.

Abstract

Tobacco smoking has emerged as a risk factor for increasing the susceptibility to infection from severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) via increased expression of angiotensin-converting enzyme-2 (ACE2) in the lung, linked to coronavirus disease 2019 (COVID-19) development. Given the modifiable nature of electronic cigarettes and the delivery of high concentrations of nicotine, we investigate whether electronic cigarette vaping has the potential to increase susceptibility to SARS-CoV-2 infection. We exposed BEAS-2B cells (bronchial epithelium transformed with Ad12-SV40 2B) and primary small airway epithelial cells (SAECs) to electronic cigarette aerosol condensates produced from propylene glycol/vegetable glycerin or commercially bought e-liquid (±added nicotine) and cigarette smoke extract to investigate if electronic cigarette exposure, like cigarette smoke, increases the expression of ACE2 in lung epithelial cells. In BEAS-2B cells, cytotoxicity (CCK-8), membrane integrity (LDH), and ACE2 protein expression (immunofluorescence) were measured for both 4- and 24 h treatments in BEAS-2B cells and 4 h in SAECs; ACE2 gene expression was measured using quantitative polymerase chain reaction (qPCR) for 4 h treatment in BEAS-2B cells. Nicotine-free condensates and higher concentrations of nicotine-containing condensates were cytotoxic to BEAS-2B cells. Higher LDH release and reduced membrane integrity were seen in BEAS-2B cells treated for 24 h with higher concentrations of nicotine-containing condensates. ACE2 protein expression was observably increased in all treatments compared to cell controls, particularly for 24 h exposures. ACE2 gene expression was significantly increased in cells exposed to the locally bought e-liquid condensate with high nicotine concentration and cigarette smoke extract compared with cell controls. Our study suggests that vaping alone and smoking alone can result in an increase in lung ACE2 expression. Vaping and smoking are avoidable risk factors for COVID-19, which, if avoided, could help reduce the number of COVID-19 cases and the severity of the disease. This is the first study to utilize electronic cigarette aerosol condensates, novel and developed in our laboratory, for investigating ACE2 expression in human airway epithelial cells.

摘要

吸烟已成为一种风险因素,通过增加肺部血管紧张素转换酶2(ACE2)的表达,使人更易感染严重急性呼吸综合征冠状病毒2(SARS-CoV-2),这与2019冠状病毒病(COVID-19)的发展有关。鉴于电子烟的可改变性质以及其高浓度尼古丁的输送,我们研究电子烟的雾化是否有可能增加对SARS-CoV-2感染的易感性。我们将BEAS-2B细胞(用Ad12-SV40 2B转化的支气管上皮细胞)和原代小气道上皮细胞(SAECs)暴露于由丙二醇/蔬菜甘油或市售电子烟液(±添加尼古丁)产生的电子烟气溶胶冷凝物以及香烟烟雾提取物中,以研究电子烟暴露是否像香烟烟雾一样会增加肺上皮细胞中ACE2的表达。在BEAS-2B细胞中,对4小时和24小时处理的BEAS-2B细胞以及4小时处理的SAECs测量细胞毒性(CCK-8)、膜完整性(LDH)和ACE2蛋白表达(免疫荧光);使用定量聚合酶链反应(qPCR)测量BEAS-2B细胞4小时处理的ACE2基因表达。不含尼古丁的冷凝物和较高浓度含尼古丁的冷凝物对BEAS-2B细胞具有细胞毒性。用较高浓度含尼古丁的冷凝物处理24小时的BEAS-2B细胞中可见较高的LDH释放和降低的膜完整性。与细胞对照相比,所有处理中ACE2蛋白表达均明显增加,尤其是24小时暴露。与细胞对照相比,暴露于高尼古丁浓度的市售电子烟液冷凝物和香烟烟雾提取物的细胞中ACE2基因表达显著增加。我们的研究表明,单独雾化和单独吸烟都会导致肺ACE2表达增加。雾化和吸烟是COVID-19可避免的风险因素,如果避免,可能有助于减少COVID-19病例数和疾病严重程度。这是第一项利用我们实验室新开发的电子烟气溶胶冷凝物来研究人呼吸道上皮细胞中ACE2表达的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/de38/7958963/df685a1bd366/jcm-10-01028-g001.jpg

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