Human Mn-superoxide dismutase in pulmonary epithelial cells of transgenic mice confers protection from oxygen injury

J Biol Chem. 1992 Nov 25;267(33):23937-41.

Abstract

To test directly whether mitochondrial Mn-superoxide dismutase (Mn-SOD) protects the lung epithelium from oxygen-induced injury, transgenic mice were produced in which the expression of human Mn-SOD mRNA was directly by transcriptional elements from the human pulmonary surfactant protein C gene. Human Mn-SOD mRNA was expressed in a lung-specific manner, and increased Mn-SOD protein was detected within mitochondria of alveolar Type II and nonciliated bronchiolar cells of the distal respiratory epithelium of the transgenic mice. The activity of Mn-SOD, but not catalase, CuZn-SOD, or glutathione peroxidase, was increased in lungs of transgenic mice. Transgenic mice were highly protected from lung injury during exposure to 95% oxygen, surviving significantly longer than nontransgenic littermates. Pulmonary pathology demonstrated decreased hemorrhage, hyaline membrane formation, and alveolar and interstitial edema in transgenic animals. The finding that increased Mn-SOD in distal respiratory epithelial cells confers protection from oxygen injury provides a basis for novel therapies to protect lung from injury during oxygen therapy of acute and chronic lung diseases.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Blotting, Northern
  • Catalase / metabolism
  • Epithelium / drug effects
  • Epithelium / enzymology
  • Epithelium / pathology
  • Female
  • Genetic Therapy
  • Glutathione Peroxidase / metabolism
  • Humans
  • Isoenzymes / genetics*
  • Isoenzymes / metabolism*
  • Lung / drug effects
  • Lung / enzymology*
  • Lung / pathology*
  • Lung Diseases / therapy
  • Male
  • Mice
  • Mice, Transgenic
  • Oxygen / toxicity*
  • RNA / genetics
  • RNA / isolation & purification
  • Restriction Mapping
  • Superoxide Dismutase / genetics*
  • Superoxide Dismutase / metabolism*

Substances

  • Isoenzymes
  • RNA
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase
  • Oxygen