PM2.5-induced airway inflammation and hyperresponsiveness in NC/Nga mice

Environ Toxicol. 2017 Mar;32(3):1047-1054. doi: 10.1002/tox.22303. Epub 2016 Jun 24.

Abstract

The allergic inflammatory effects of particulate matter (PM) 2.5, collected with the cyclone system in Yokohama city in Japan, were investigated in NC/Nga mice, which are hypersensitive to mite allergens. PM2.5 with alum was injected intraperitoneally for sensitization. Five days later, 200 μg of PM2.5 in 25 μL of saline was administered to mice intranasally five times for further sensitization. On the 11th day, PM2.5 was administered as a challenge. On the 12th day, mice were examined for airway hyperresponsiveness (AHR), the bronchoalveolar lavage fluid (BALF) cell count, mRNA expression of Th1 , Th2 cytokines, and metallothioneins in lung tissue, and histopathology. PM2.5 increased AHR, total cell numbers including eosinophils in BALF, and mRNA levels of IL-5, IL-22, eotaxin, eotaxin 2, and metallothionein 3. In PM2.5-induced lungs, inflammation was observed around the bronchus. These results demonstrate that PM2.5 alone, collected with the cyclone system in Yokohama city in Japan, induces asthma-like airway inflammation. © 2016 Wiley Periodicals, Inc. Environ Toxicol 32: 1047-1054, 2017.

Keywords: NC/Nga mice; PM2.5; allergic airway inflammation.

MeSH terms

  • Animals
  • Asthma / chemically induced
  • Asthma / pathology
  • Asthma / physiopathology
  • Bronchial Hyperreactivity / chemically induced*
  • Bronchial Hyperreactivity / immunology
  • Bronchial Hyperreactivity / pathology
  • Bronchial Hyperreactivity / physiopathology
  • Bronchoalveolar Lavage Fluid / chemistry
  • Cytokines / metabolism
  • Inflammation / chemically induced
  • Inflammation / metabolism
  • Lung / drug effects
  • Lung / metabolism
  • Lung / pathology
  • Male
  • Mice
  • Mice, Inbred Strains
  • Particle Size
  • Particulate Matter / toxicity*
  • Pneumonia / chemically induced*
  • Pneumonia / immunology
  • Pneumonia / pathology
  • Pneumonia / physiopathology*

Substances

  • Cytokines
  • Particulate Matter