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Generation of Electronic Cigarette Aerosol by a Third-Generation Machine-Vaping Device: Application to Toxicological Studies
Published on: August 25, 2018
Electronic Nicotine Delivery System Aerosol-induced Cell Death and Dysfunction in Macrophages and Lung Epithelial
Gregory L Serpa1, Nicholas D Renton1, Nari Lee1
1Division of Biology and Medicine, Department of Molecular Microbiology and Immunology, Brown University, Providence, Rhode Island.
Abstract:
Electronic nicotine delivery system (ENDS) use is outpacing our understanding of its potential harmful effects. Homeostasis of the lung is maintained through proper balance of cell death, efferocytic clearance, and phagocytosis of pathogens. To investigate whether ENDS use has the potential to alter this balance, we developed physiologically relevant ENDS exposure paradigms for lung epithelial cells and primary macrophages. In our studies, cells were exposed directly to aerosol made from carefully controlled components with and without nicotine. We found that ENDS aerosol exposure led to apoptosis, secondary necrosis, and necrosis in lung epithelial cell models. In contrast, macrophages died mostly by apoptosis and inflammatory caspase-mediated cell death when exposed to ENDS aerosol. The clearance of dead cells and pathogens by efferocytosis and phagocytosis, respectively, is an important process in maintaining a healthy lung. To investigate the impact of ENDS aerosol on macrophage function independent of general toxicity, we used an exposure time that did not induce cell death in primary macrophages. Exposure to ENDS aerosol containing nicotine inhibited nearly all phagocytic and greatly reduced the efferocytic abilities of primary macrophages. When challenged with a bacterial pathogen, there was decreased bacterial clearance. The presence of nicotine in the ENDS aerosol increased its toxicity and functional impact; however, nicotine exposure alone did not have any deleterious effects. These data demonstrate that ENDS aerosol exposure could lead to increased epithelial cell and macrophage death in the lung and impair important macrophage functions that are essential for maintenance of lung function.
Insights
Electronic nicotine delivery system (ENDS) aerosol harms lung homeostasis by increasing cell death and impairing macrophage function. Nicotine exacerbates these ENDS effects, impacting lung health.
Area of Science:
- Pulmonary toxicology
- Cellular biology
- Immunology
Background:
- Lung homeostasis relies on balanced cell death, efferocytosis, and phagocytosis.
- Electronic nicotine delivery system (ENDS) use is rising, but its lung health effects are not fully understood.
Purpose of the Study:
- To investigate the impact of ENDS aerosol on lung epithelial cells and macrophages.
- To determine if ENDS aerosol alters lung homeostasis by affecting cell death and macrophage function.
Main Methods:
- Developed physiologically relevant ENDS exposure models for lung epithelial cells and primary macrophages.
- Exposed cells directly to ENDS aerosol with and without nicotine.
- Assessed cell death (apoptosis, necrosis) and macrophage phagocytic/efferocytic functions.
Main Results:
- ENDS aerosol induced apoptosis, secondary necrosis, and necrosis in lung epithelial cells.
- Macrophages exposed to ENDS aerosol died primarily via apoptosis and inflammatory caspase-mediated pathways.
- Nicotine-containing ENDS aerosol significantly inhibited macrophage phagocytosis and efferocytosis, reducing bacterial clearance.
- Nicotine alone did not cause these deleterious effects, indicating aerosol components are key.
Conclusions:
- ENDS aerosol exposure can increase lung epithelial and macrophage cell death.
- ENDS aerosol impairs critical macrophage functions essential for lung health.
- Nicotine potentiates the toxic and functional impacts of ENDS aerosol on lung cells.
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