Transcriptional control of human diploid fibroblast collagen synthesis by γ-interferon

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Abstract

Recombinant γ-interferon (rec γ-IFN) caused potent inhibition of collagen synthesis by cultured confluent human diploid fibroblasts in a dose-dependent manner. Gel electrophoresis of the newly synthesized proteins from the culture media of rec γ-IFN-treated fibroblasts demonstrated a selective depression of procollagen without a significant change in non-collagenous proteins. Dot blot hybridization to a Type I procollagen cDNA probe showed that the inhibition of collagen production was accompanied by a decrease in the levels of collagen mRNA. These results indicate that rec γ-IFN is capable of exerting transcriptional modulation of collagen biosynthesis and suggest that it may play an important role in regulation of normal and pathologic fibrogenesis.

References (15)

  • S.R. Pinnell

    J. Invest. Dermatol

    (1982)
  • K. Juva et al.

    Anal. Biochem

    (1966)
  • W. Burnett et al.

    Biochem. Biophys. Res. Commun

    (1979)
  • J.C. Myers et al.

    J. Biol. Chem

    (1983)
  • E.C. LeRoy

    J. Clin. Invest

    (1974)
  • R.L. Johnson et al.

    J. Clin. Invest

    (1976)
  • S.M. Wahl et al.

    J. Immunol

    (1978)
There are more references available in the full text version of this article.

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