Interferon-{beta} inhibits bleomycin-induced lung fibrosis by decreasing transforming growth factor-{beta} and thrombospondin

Am J Respir Cell Mol Biol. 2005 Feb;32(2):93-8. doi: 10.1165/rcmb.2003-0374OC. Epub 2004 Nov 19.

Abstract

Pulmonary fibrosis is the result of abnormal processes of repair that occur after lung injury. Transforming growth factor (TGF)-beta is a key molecule in the progression of pulmonary fibrosis. Although clinical use of interferon (IFN)-beta did not improve survival in patients with idiopathic pulmonary fibrosis, because some preclinical studies have suggested that IFN-beta is a potent inhibitor of fibrogenesis, beneficial effects of IFN-beta have been expected. We therefore attempted to determine effects of IFN-beta and investigated the mechanism of action of IFN-beta in bleomycin-induced pulmonary fibrosis. Bleomycin at Day 0 and IFN-beta for 4 wk were administered intravenously to ICR mice. At 28 d after bleomycin injection, histologic and chemical analysis was performed for evaluation of effects of IFN-beta. Tissue distribution and amounts of TGF-beta1 and thrombospondin (TSP)-1/2 were analyzed. IFN-beta attenuated prolylhydroxylase activity, resulting in inhibition of pulmonary fibrosis. Bleomycin-induced increase in TGF-beta1 in epithelial cells and extracellular matrix was attenuated by IFN-beta. TSP-1/2 was limited in platelets of control mice, but was present in foamy cells in fibrotic regions induced by bleomycin. These findings suggest that the antifibrotic effect of IFN-beta is inhibition of TGF-beta and its activation via decrease in TSP-1/2 in lung tissue and change in location of TSP-1/2 from platelets to foamy cells.

MeSH terms

  • Animals
  • Antibiotics, Antineoplastic / administration & dosage*
  • Bleomycin / administration & dosage*
  • Epithelial Cells / metabolism
  • Epithelial Cells / pathology
  • Extracellular Matrix / metabolism
  • Foam Cells / metabolism
  • Foam Cells / pathology
  • Immunohistochemistry
  • Interferon-beta / administration & dosage*
  • Lung / metabolism
  • Lung / pathology
  • Male
  • Mice
  • Mice, Inbred ICR
  • Procollagen-Proline Dioxygenase / metabolism
  • Pulmonary Fibrosis / chemically induced
  • Pulmonary Fibrosis / metabolism*
  • Pulmonary Fibrosis / pathology
  • Thrombospondin 1 / metabolism*
  • Thrombospondins / metabolism*
  • Transforming Growth Factor beta / metabolism*
  • Transforming Growth Factor beta1

Substances

  • Antibiotics, Antineoplastic
  • Tgfb1 protein, mouse
  • Thrombospondin 1
  • Thrombospondins
  • Transforming Growth Factor beta
  • Transforming Growth Factor beta1
  • thrombospondin 2
  • Bleomycin
  • Interferon-beta
  • Procollagen-Proline Dioxygenase