A Review of Pulmonary Neutrophilia and Insights into the Key Role of Neutrophils in Particle-Induced Pathogenesis in the Lung from Animal Studies of Lunar Dusts and Other Poorly Soluble Dust Particles

Details

• Personal Author:
  Castranova, Vincent ; Crucian B ; Driscoll K ; Gardner D ; Hunter R ; James J ; Lam C-w ; McClellan R ; McCluskey R ; Nelman M ; Renne R ; Ryder V ; Scully R ; Wallace W ; Warheit D ; Zeidler-Erdely P ; Zhang Y
• Description:
  The mechanisms of particle-induced pathogenesis in the lung remain poorly understood. Neutrophilic inflammation and oxidative stress in the lung are hallmarks of toxicity. Some investigators have postulated that oxidative stress from particle surface reactive oxygen species (psROS) on the dust produces the toxicopathology in the lungs of dust-exposed animals. This postulate was tested concurrently with the studies to elucidate the toxicity of lunar dust (LD), which is believed to contain psROS due to high-speed micrometeoroid bombardment that fractured and pulverized lunar surface regolith. Results from studies of rats intratracheally instilled (ITI) with three LDs (prepared from an Apollo-14 lunar regolith), which differed 14-fold in levels of psROS, and two toxicity reference dusts (TiO2 and quartz) indicated that psROS had no significant contribution to the dusts' toxicity in the lung. Reported here are results of further investigations by the LD toxicity study team on the toxicological role of oxidants in alveolar neutrophils that were harvested from rats in the 5-dust ITI study and from rats that were exposed to airborne LD for 4 weeks. The oxidants per neutrophils and all neutrophils increased with dose, exposure time and dust's cytotoxicity. The results suggest that alveolar neutrophils play a critical role in particle-induced injury and toxicity in the lung of dust-exposed animals. Based on these results, we propose an adverse outcome pathway (AOP) for particle-associated lung disease that centers on the crucial role of alveolar neutrophil-derived oxidant species. A critical review of the toxicology literature on particle exposure and lung disease further supports a neutrophil-centric mechanism in the pathogenesis of lung disease and may explain previously reported animal species differences in responses to poorly soluble particles. Key findings from the toxicology literature indicate that (1) after exposures to the same dust at the same amount, rats have more alveolar neutrophils than hamsters; hamsters clear more particles from their lungs, consequently contributing to fewer neutrophils and less severe lung lesions; (2) rats exposed to nano-sized TiO2 have more neutrophils and more severe lesions in their lungs than rats exposed to the same mass-concentration of micron-sized TiO2; nano-sized dust has a greater number of particles and a larger total particle-cell contact surface area than the same mass of micron-sized dust, which triggers more alveolar epithelial cells (AECs) to synthesize and release more cytokines that recruit a greater number of neutrophils leading to more severe lesions. Thus, we postulate that, during chronic dust exposure, particle-inflicted AECs persistently release cytokines, which recruit neutrophils and activate them to produce oxidants resulting in a prolonged continuous source of endogenous oxidative stress that leads to lung toxicity. This neutrophil-driven lung pathogenesis explains why dust exposure induces more severe lesions in rats than hamsters; why, on a mass-dose basis, nano-sized dusts are more toxic than the micron-sized dusts; why lung lesions progress with time; and why dose-response curves of particle toxicity exhibit a hockey stick like shape with a threshold. The neutrophil centric AOP for particle-induced lung disease has implications for risk assessment of human exposures to dust particles and environmental particulate matter. [Description provided by NIOSH]
• Subjects:
  Animals Dust Immune System Lung Occupational Health Particulate Matter Respiratory System Safety Toxicology
• Keywords:
  Animal Studies Author Keywords: Lunar Dust Cytokines Diesel Particles Dust Particles Immune Reaction Inhalation Studies Inhalation Toxicity Intratracheal Instillation Lung Irritants Lung Pathogenesis Mechanism Of Toxicity Moon Dust Neutrophilia Neutrophils Oxidative Stress Particulate Matter Particulates Pathogenesis PM PSP Pulmonary Effects ROS Toxicopathology

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• ISSN:
  1040-8444
• Document Type:
  Text
• Genre:
  Journal Article
• Place as Subject:
  Delaware ; Florida ; Georgia ; New Jersey ; New Mexico ; Oklahoma ; OSHA Region 10 ; OSHA Region 2 ; OSHA Region 3 ; OSHA Region 4 ; OSHA Region 6 ; Texas ; Washington ; West Virginia
• CIO:
  National Institute for Occupational Safety and Health (NIOSH)
• Division:
  HELD - Health Effects Laboratory Division
• Topic:
  Workplace Safety & Health
• Location:
  North America
• Pages in Document:
  441-479
• Volume:
  53
• Issue:
  8
• NIOSHTIC Number:
  nn:20068640
• Citation:
  Crit Rev Toxicol 2023 Sep; 53(8):441-479
• Contact Point Address:
  Chiu-wing Lam, Biomedical Research and Environmental Sciences Division, NASA Johnson Space Center, Houston, TX, USA
• Email:
  chiu-wing.lam-1@nasa.gov
• Federal Fiscal Year:
  2023
• Peer Reviewed:
  True
• Source Full Name:
  Critical Reviews in Toxicology
• Collection(s):
  National Institute for Occupational Safety and Health
• Main Document Checksum:
  urn:sha-512:4dfa3e758d8849a43c297db244ab2d12c1f46b6296b1a559bef308fc8972db1be073060b05397783947bc20623de36717ec243d6a76d048acd1054959f117a6c
• Download URL:
  https://stacks.cdc.gov/view/cdc/207241/cdc_207241_DS1.pdf
• File Type:
  [PDF - 7.24 MB ]