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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
E-cigarette-induced changes in cell stress and mitochondrial function
Ramamurthy Chitteti1, Juan Pablo Zuniga-Hertz1, Jorge A Masso-Silva2
1VA San Diego Healthcare System, San Diego, CA, USA; Department of Anesthesiology, School of Medicine, University of California San Diego, USA.
Electronic cigarette (e-cig) use alters blood exosomes and mitochondrial function. E-cig aerosols harm cells, increasing stress and inflammation risk.
Area of Science:
- Biomedical Science
- Toxicology
- Cell Biology
Background:
- Electronic nicotine delivery systems (e-cigarettes or e-cigs) are increasingly popular.
- Inhaling e-cig aerosols may cause health issues beyond nicotine addiction.
- E-cig aerosol exposure can impact cellular processes and lead to chronic diseases.
Purpose of the Study:
- To investigate the effects of e-cig use on circulating exosome profiles in young adults.
- To assess markers of cell stress in e-cig users.
- To determine how plasma from e-cig users affects mitochondrial function in human cells.
Main Methods:
- Analysis of plasma exosome profiles and biomarkers (mtDNA, protein carbonyls, 4-HNE) in e-cig users and non-users.
- In vitro study using endothelial (EA.hy926) and epithelial (A549) cells exposed to plasma from e-cig users.
- Assessment of mitochondrial respiration, metabolic stress, mitochondrial membrane potential (MMP), and reactive oxygen species (ROS) levels.
Main Results:
- E-cig users exhibited altered plasma exosome profiles with increased cell-free mitochondrial DNA (mtDNA), protein carbonyls, and 4-HNE.
- Plasma from e-cig users reduced maximal mitochondrial respiration and spare capacity in exposed cells.
- Increased metabolic stress, altered mitochondrial morphology, elevated MMP, and heightened ROS levels were observed in cells exposed to e-cig user plasma.
Conclusions:
- E-cig use leads to significant alterations in plasma exosome profiles and increased markers of mitochondrial stress.
- Circulating factors in e-cig user plasma drive metabolic stress in endothelial and epithelial cells.
- E-cig use adversely affects mitochondrial function, potentially contributing to chronic inflammation.
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