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.

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.