Granulocyte colony-stimulating factor decreases tumor necrosis factor production in whole blood: role of interleukin-10 and prostaglandin E(2)

Eur Cytokine Netw. 2004 Oct-Dec;15(4):323-6.

Abstract

Previous reports have indicated that the administration of granulocyte colony-stimulating factor (G-CSF) decreases ex vivo tumor necrosis factor (TNF) production in humans. In this study, we report that daily pretreatment of mice with G-CSF for three days decreases ex vivo lipopolysaccharide (LPS)-induced TNF production in whole blood. Conversely, production of interleukin-10 (IL-10) and prostaglandin E(2) (PGE(2)) is increased. The inhibitory effect of G-CSF pretreatment on TNF production is partially reversed by addition of an anti-IL-10 antibody, and completely reversed by combined addition of anti-IL-10 antibody and the cyclooxygenase (COX) inhibitor, ketoprofen. These results suggest that G-CSF decreases TNF production in this experimental model by increasing production of IL-10 and PGE(2), which are both known inhibitors of TNF production.

MeSH terms

  • Animals
  • Blood Cells / physiology*
  • Cells, Cultured
  • Dinoprostone / biosynthesis*
  • Granulocyte Colony-Stimulating Factor / administration & dosage*
  • In Vitro Techniques
  • Injections, Subcutaneous
  • Interleukin-10 / biosynthesis*
  • Lipopolysaccharides / toxicity*
  • Mice
  • Tumor Necrosis Factors / biosynthesis*

Substances

  • Lipopolysaccharides
  • Tumor Necrosis Factors
  • Interleukin-10
  • Granulocyte Colony-Stimulating Factor
  • Dinoprostone