4.8 Article

Pulmonary Exposure to Magneli Phase Titanium Suboxides Results in Significant Macrophage Abnormalities and Decreased Lung Function

Journal

FRONTIERS IN IMMUNOLOGY
Volume 10, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2019.02714

Keywords

cytotoxicity; air pollution; nanoparticle; TixO2x-1; in vivo; environmental exposure

Categories

Funding

  1. Virginia-Maryland College of Veterinary Medicine
  2. National Natural Science Foundation of China [41522111, 4176114462]
  3. Center for the Environmental Implications of Nanotechnology (NSF) [EF-0830093]
  4. Virginia Tech Institute for Critical Technology and Applied Science (ICTAS)
  5. Open Foundation of East China Normal University
  6. Virginia Tech National Center for Earth and Environmental Nanotechnology Infrastructure (NSF) [ECCS-1542100]
  7. STAR Fellowship Assistance Agreement - U.S. Environmental Protection Agency (EPA) [FP-91780101-1]
  8. National Institutes of Health [R01 ES019311]
  9. National Institute of Allergy and Infectious Diseases Animal Model Research for Veterinarians (AMRV) training grant [T32-OD010430]
  10. American Association of Immunologist Careers in Immunology Fellowship Program

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Coal is one of the most abundant and economic sources for global energy production. However, the burning of coal is widely recognized as a significant contributor to atmospheric particulate matter linked to deleterious respiratory impacts. Recently, we have discovered that burning coal generates large quantities of otherwise rare Magneli phase titanium suboxides from TiO2 minerals naturally present in coal. These nanoscale Magneli phases are biologically active without photostimulation and toxic to airway epithelial cells in vitro and to zebrafish in vivo. Here, we sought to determine the clinical and physiological impact of pulmonary exposure to Magneli phases using mice as mammalian model organisms. Mice were exposed to the most frequently found Magneli phases, Ti6O11, at 100 parts per million (ppm) via intratracheal administration. Local and systemic titanium concentrations, lung pathology, and changes in airway mechanics were assessed. Additional mechanistic studies were conducted with primary bone marrow derived macrophages. Our results indicate that macrophages are the cell type most impacted by exposure to these nanoscale particles. Following phagocytosis, macrophages fail to properly eliminate Magneli phases, resulting in increased oxidative stress, mitochondrial dysfunction, and ultimately apoptosis. In the lungs, these nanoparticles become concentrated in macrophages, resulting in a feedback loop of reactive oxygen species production, cell death, and the initiation of gene expression profiles consistent with lung injury within 6 weeks of exposure. Chronic exposure and accumulation of Magneli phases ultimately results in significantly reduced lung function impacting airway resistance, compliance, and elastance. Together, these studies demonstrate that Magneli phases are toxic in the mammalian airway and are likely a significant nanoscale environmental pollutant, especially in geographic regions where coal combustion is a major contributor to atmospheric particulate matter.

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