Proteoglycans decorin and biglycan differentially modulate TGF-beta-mediated fibrotic responses in the lung

Am J Physiol Lung Cell Mol Physiol. 2001 Jun;280(6):L1327-34. doi: 10.1152/ajplung.2001.280.6.L1327.

Abstract

Transforming growth factor (TGF)-beta is a key cytokine in the pathogenesis of pulmonary fibrosis, and pharmacological interference with TGF-beta can ameliorate the fibrotic tissue response. The small proteoglycans decorin and biglycan are able to bind and inhibit TGF-beta activity in vitro. Although decorin has anti-TGF-beta properties in vivo, little is known about the physiological role of biglycan in vivo. Adenoviral gene transfer was used to overexpress active TGF-beta, decorin, and biglycan in cell culture and in murine lungs. Both proteoglycans were able to interfere with TGF-beta bioactivity in vitro in a dose-dependant manner. In vivo, overexpression of TGF-beta resulted in marked lung fibrosis, which was significantly reduced by concomitant overexpression of decorin. Biglycan, however, had no significant effect on lung fibrosis induced by TGF-beta. The data suggest that differences in tissue distribution are responsible for the different effects on TGF-beta bioactivity in vivo, indicating that decorin, but not biglycan, has potential therapeutic value in fibrotic disorders of the lung.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae / genetics
  • Animals
  • Biglycan
  • Bronchoalveolar Lavage Fluid / chemistry
  • Bronchoalveolar Lavage Fluid / cytology
  • Cell Line
  • Decorin
  • Dose-Response Relationship, Drug
  • Extracellular Matrix Proteins
  • Female
  • Fibroblasts / cytology
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Gene Transfer Techniques
  • Genetic Vectors / genetics
  • Genetic Vectors / metabolism
  • Genetic Vectors / pharmacology
  • Humans
  • Hydroxyproline / metabolism
  • Immunohistochemistry
  • Lung / metabolism*
  • Lung / pathology
  • Mice
  • Mice, Inbred C57BL
  • Proteoglycans / genetics
  • Proteoglycans / metabolism
  • Proteoglycans / pharmacology*
  • Pulmonary Fibrosis / chemically induced
  • Pulmonary Fibrosis / metabolism
  • Pulmonary Fibrosis / pathology
  • Pulmonary Fibrosis / prevention & control*
  • Tissue Distribution
  • Transforming Growth Factor beta / antagonists & inhibitors*
  • Transforming Growth Factor beta / biosynthesis
  • Transforming Growth Factor beta / genetics
  • Treatment Outcome

Substances

  • BGN protein, human
  • Bgn protein, mouse
  • Biglycan
  • DCN protein, human
  • Dcn protein, mouse
  • Decorin
  • Extracellular Matrix Proteins
  • Proteoglycans
  • Transforming Growth Factor beta
  • Hydroxyproline