Regulation of collagen synthesis and mRNA expression in normal and hypertrophic scar fibroblasts in vitro by interferon-gamma

J Surg Res. 1995 May;58(5):471-7. doi: 10.1006/jsre.1995.1074.

Abstract

Development of hypertrophic scarring (HTS) is a major problem for patients who survive extensive thermal injuries. HTS and other fibroproliferative disorders are associated with excessive accumulation of collagen and other extracellular matrix proteins. Recent in vitro and in vivo studies have demonstrated that proteins of the interferon family have an inhibitory effect on collagen production by fibroblasts in some fibroproliferative disorders. This study investigated the effects of interferon-gamma (IFN-gamma) on cell proliferation, collagen production, and expression of types I and III procollagen mRNA in human postburn HTS fibroblasts. Paired fibroblast cultures were established from explants of biopsies obtained from HTS and normal skin (matched for location and skin tension) in five patients recovering from thermal injuries. Thus, normal dermis from each patient was used as a paired control. Administration of IFN-gamma (1000 U/ml) to proliferating fibroblast cultures for 5 days resulted in 51% reduction (P < 0.05) in HTS cell proliferation. Using hydroxyproline as an index for collagen production, a 34% reduction (P < 0.05) in collagen synthesis was observed in HTS fibroblast culture media after treatment with IFN-gamma (1000 u/ml) for 48 hr. Northern blot analysis demonstrated 55 and 36% reductions (P < 0.05 for each) in type I and type III procollagen mRNA levels, respectively, after treatment for 12 hr with IFN-gamma (1000 u/ml). The effect of IFN-gamma on each of these parameters was at least as pronounced in HTS fibroblasts as their normal controls.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Cell Division / drug effects
  • Cells, Cultured
  • Child
  • Cicatrix, Hypertrophic / metabolism*
  • Cicatrix, Hypertrophic / pathology
  • Collagen / biosynthesis*
  • Collagen / genetics*
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Humans
  • Infant
  • Interferon-gamma / pharmacology*
  • Male
  • Middle Aged
  • Procollagen / genetics
  • RNA, Messenger / metabolism*
  • Reference Values

Substances

  • Procollagen
  • RNA, Messenger
  • Interferon-gamma
  • Collagen