Differential expression of EC-SOD, Mn-SOD and CuZn-SOD in rat lung exposed to crystalline silica

J Occup Health. 2007 May;49(3):242-8. doi: 10.1539/joh.49.242.

Abstract

Superoxide dismutases (SODs) are antioxidant enzymes that catalyze the dismutation of superoxide into hydrogen peroxide. There are 3 kinds of isozymes: extracellular superoxide dismutase (EC-SOD), manganese-containing superoxide dismutase (Mn-SOD) and copper- and zinc-containing superoxide dismutase (CuZn-SOD). To examine the expression of SOD isozymes in lungs injured by crystalline silica, we intratracheally instilled male Wistar rats with 2 mg (8 mg/kg) of crystalline silica and investigated the mRNA, protein level and distribution of SOD isozymes in the rat lungs using RT-PCR, western blot analysis and immunostaining, respectively at from 3 d to 180 d of recovery following the exposure. EC-SOD mRNA levels significantly increased from 3 d to 90 d and the EC-SOD protein level was significantly higher after 90 and 180 d recovery in the crystalline silica exposed groups than in the control groups. Mn-SOD increased in silica treated rat lungs at both mRNA and protein levels, peaking at 30 d post-exposure. CuZn-SOD mRNA levels were decreased at 3, 7 and 30 d, and CuZn-SOD protein levels were also significantly lower than the control group at 90 and 180 d recovery. There was prominent EC-SOD immunostaining mainly in the plasma and alveolar macrophages and strong Mn-SOD staining in alveolar macrophages and interstitial cells of the proximal and distal portions of the alveolar duct following crystalline silica exposure. There was less CuZn-SOD staining in epithelial cells at terminal bronchioles in the crystalline silica-exposed group. These findings suggest that these SOD isozymes may be related to lung injury induced by crystalline silica.

MeSH terms

  • Animals
  • Japan
  • Lung / enzymology*
  • Lung Injury*
  • Male
  • Polymerase Chain Reaction / methods
  • Rats
  • Rats, Wistar
  • Silicon Dioxide / administration & dosage*
  • Silicon Dioxide / pharmacology
  • Superoxide Dismutase / analysis*
  • Superoxide Dismutase / metabolism

Substances

  • Silicon Dioxide
  • Sod3 protein, rat
  • Superoxide Dismutase