Cytokine-induced upregulation of hepatic intercellular adhesion molecule-1 messenger RNA expression and its role in the pathophysiology of murine endotoxin shock and acute liver failure

Hepatology. 1995 Jun;21(6):1632-9.

Abstract

Neutrophil-induced liver injury during endotoxemia is dependent on the adhesion molecule Mac-1 (CD11b/CD18) on neutrophils. The potential involvement of its counterreceptor, intercellular adhesion molecule-1 (ICAM-1), in the pathogenesis was investigated after administration of 100 micrograms/kg Salmonella abortus equi endotoxin (ET) in galactosamine-sensitized mice (Gal). In ET-sensitive mice (C3Heb/FeJ), which generated large amounts of tumor necrosis factor-alpha (TNF-alpha), massive neutrophil infiltration and severe liver injury were observed. In an ET-resistant strain (C3H/HeJ), which did not generate TNF-alpha Gal/ET failed to cause neutrophil accumulation or injury. ICAM-1 messenger RNA (mRNA), negligible in control livers, was selectively induced by Gal/ET in ET-sensitive mice. Intravenous injection of murine TNF-alpha, interleukin-1 alpha (IL-1 alpha) or IL-I beta (13 to 23 micrograms/kg) strongly induced the ICAM-1 message in both strains, showing a comparable capacity for ICAM-1 mRNA synthesis. All cytokines caused similar neutrophil accumulation in the liver; however, only Gal/TNF-alpha also caused upregulation of Mac-1 on circulating neutrophils and liver injury. The anti-murine ICAM-1 monoclonal antibody YN.1 (3 mg/kg) attenuated liver injury in ET-sensitive mice by 67% to 90% compared with isotype-matched control antibody-treated animals but did not reduce neutrophil accumulation in hepatic sinusoids. Our data suggest that the cytokines TNF-alpha and IL-1 are the main mediators responsible for upregulation of ICAM-1 mRNA in the liver during endotoxemia. The upregulation of both adhesion molecules, ICAM-1 and Mac-1, is necessary for a neutrophil-induced liver injury to occur. (ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Cytokines / pharmacology*
  • DNA Primers
  • Endotoxins / toxicity
  • Flow Cytometry
  • Gene Expression Regulation / drug effects*
  • Intercellular Adhesion Molecule-1 / biosynthesis*
  • Interleukin-1 / pharmacology
  • Liver / drug effects
  • Liver / pathology
  • Liver / physiopathology*
  • Liver Failure, Acute / pathology
  • Liver Failure, Acute / physiopathology*
  • Male
  • Mice
  • Mice, Inbred C3H
  • Molecular Sequence Data
  • Neutrophils / drug effects
  • Neutrophils / physiology*
  • Polymerase Chain Reaction
  • RNA, Messenger / biosynthesis
  • Salmonella
  • Shock, Septic / pathology
  • Shock, Septic / physiopathology*
  • Species Specificity
  • Tumor Necrosis Factor-alpha / pharmacology

Substances

  • Cytokines
  • DNA Primers
  • Endotoxins
  • Interleukin-1
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Intercellular Adhesion Molecule-1