Interleukin 6 modulates c-sis gene expression in cultured human endothelial cells

Cell Immunol. 1992 Aug;143(1):118-26. doi: 10.1016/0008-8749(92)90010-m.

Abstract

Human vascular endothelial cells secrete platelet-derived growth factor (PDGF)-like polypeptides which may mediate some of the vascular effects in the inflammatory process. We have demonstrated that IL-6 caused a significant increase in the mRNA level of the c-sis gene (PDGF B chain) in cultured human endothelial cells. IL-1 alpha and IL-1 beta also increased c-sis mRNA transcripts after an extended incubation period and both cytokines acted synergistically with IL-6 in increasing c-sis expression. Tumor necrosis factor enhanced the accumulation of c-sis mRNA and interferon-gamma decreased its level. In the inflammatory process specific cytokines can modulate c-sis expression in human endothelial cells. Their subsequent production of PDGF-like polypeptides could stimulate cell migration and proliferation, and cause the release of vascular inflammatory mediators.

Publication types

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

MeSH terms

  • Cells, Cultured
  • Endothelium, Vascular / metabolism*
  • Gene Expression / drug effects*
  • Humans
  • Interferon-gamma / pharmacology
  • Interleukin-1 / pharmacology
  • Interleukin-6 / pharmacology*
  • Platelet-Derived Growth Factor / genetics*
  • Proto-Oncogene Proteins / genetics*
  • Proto-Oncogene Proteins c-sis
  • Proto-Oncogenes*
  • Receptors, Immunologic / genetics
  • Receptors, Interleukin-6
  • Recombinant Proteins / pharmacology
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Interleukin-1
  • Interleukin-6
  • Platelet-Derived Growth Factor
  • Proto-Oncogene Proteins
  • Proto-Oncogene Proteins c-sis
  • Receptors, Immunologic
  • Receptors, Interleukin-6
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma