Induction of CINC (interleukin-8) production in rat liver by non-parenchymal cells

J Gastroenterol Hepatol. 1998 Jul;13(7):696-702. doi: 10.1111/j.1440-1746.1998.tb00716.x.

Abstract

The production of interleukin-8 (CINC: cytokine-induced neutrophil chemo-attractant) from different cell populations in the rat liver was studied and cells related to the initiation of CINC production in lipopolysaccharide (LPS)-injected endotoxaemic rats were characterized. Sinusoidal endothelial cells (16.4 +/- 10.6 ng/mL) produced significantly higher amounts of CINC in 24 h primary cultures compared with hepatocytes (0.9 +/- 0.9 ng/mL; P < 0.05) and Kupffer cells (6.5 +/- 5.1 ng/mL; P < 0.05). Lipopolysaccharide, tumour necrosis factor-alpha (TNF-alpha), and interleukin-1 alpha (IL-1 alpha) stimulated different liver cell populations to produce CINC; LPS mainly stimulated Kupffer cells. TNF-alpha stimulated hepatocytes and IL-1 alpha stimulated all three types of cells. Intraperitoneal injection of LPS (4 mg/kg) caused CINC accumulation in non-parenchymal cells of the rat liver within 1 h of injection, as shown by immunohistochemical staining. In contrast, CINC-positive hepatocytes were not seen until 3 h after injection of LPS. Ethanol was not a direct inducer of CINC production by rat hepatocytes in vitro. These findings strongly suggest that non-parenchymal liver cells, including sinusoidal endothelial cells, are the main source of CINC. Our data also suggest that during endotoxaemia, CINC production is initiated by non-parenchymal cells and this is followed by production from hepatocytes.

Publication types

  • Comparative Study

MeSH terms

  • Animals
  • Cells, Cultured
  • Chemokines, CXC / metabolism*
  • Chemotactic Factors / metabolism*
  • Ethanol / pharmacology
  • Growth Inhibitors / metabolism*
  • Growth Substances / metabolism*
  • Intercellular Signaling Peptides and Proteins*
  • Interleukin-1 / pharmacology
  • Interleukin-8 / metabolism*
  • Kupffer Cells / metabolism
  • Lipopolysaccharides / pharmacology
  • Liver / cytology
  • Liver / metabolism*
  • Male
  • Rats
  • Rats, Sprague-Dawley
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Chemokines, CXC
  • Chemotactic Factors
  • Growth Inhibitors
  • Growth Substances
  • Intercellular Signaling Peptides and Proteins
  • Interleukin-1
  • Interleukin-8
  • Lipopolysaccharides
  • Tumor Necrosis Factor-alpha
  • Ethanol