Tumour necrosis factor-alpha-induced expression of intercellular adhesion molecule-1 on human eosinophilic leukaemia EoL-1 cells is mediated by the activation of nuclear factor-kappaB pathway

Clin Exp Allergy. 2003 Feb;33(2):241-8. doi: 10.1046/j.1365-2222.2003.01585.x.

Abstract

Background: Intercellular adhesion molecule-1 (ICAM-1) has been shown to mediate the adhesion and migration of eosinophils to the site of allergic inflammation. However, molecular mechanisms regulating the expression of ICAM-1 in eosinophils are still being elucidated. We investigated the effect of tumour necrosis factor-alpha (TNF-alpha) on ICAM-1 expression of eosinophils.

Methods: The surface expression of ICAM-1 on a human eosinophilic leukaemic cell line, EoL-1, was assessed by immunocytochemical staining. The phosphorylation of inhibitor kappa B-alpha (IkappaB-alpha) and p38 mitogen-activated protein kinase (MAPK) was detected by Western blot. Nuclear factor kappa-B (NF-kappaB) pathway-related genes were evaluated by the cDNA expression array system, whereas the activity of NF-kappaB was measured by electrophoretic mobility shift assay (EMSA).

Results: TNF-alpha was found to induce the cell surface expression of ICAM-1. A specific proteasome inhibitor N-cbz-Leu-Leu-leucinal (MG-132), but not a p38 MAPK inhibitor (SB 203580), was found to suppress the TNF-alpha-induced expression of ICAM-1 on EoL-1 cells. The gene expressions of ICAM-1, NF-kappaB and IkappaBalpha were up-regulated after the stimulation with TNF-alpha. Further, TNF-alpha was shown to induce IkappaB-alpha phosphorylation and degradation, thereby indicating the activation of NF-kappaB. In EMSA, there was a shifted NF-kappaB band on TNF-alpha-treated cells with or without SB 203580, but no shifted band was observed on MG-132-treated cells.

Conclusion: In vitro studies of EoL-1 cells, an eosinophilic leukaemic cell line, confirmed that NF-kappaB plays an important role in the expression of ICAM-1 and recruitment of eosinophils in allergic inflammation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Enzyme Inhibitors / pharmacology
  • Eosinophils / metabolism*
  • Gene Expression Regulation / drug effects
  • Humans
  • Hypereosinophilic Syndrome / metabolism
  • I-kappa B Proteins / metabolism
  • Imidazoles / pharmacology
  • Intercellular Adhesion Molecule-1 / metabolism*
  • Leupeptins / pharmacology
  • Mitogen-Activated Protein Kinases / physiology
  • NF-KappaB Inhibitor alpha
  • NF-kappa B / physiology*
  • Phosphorylation / drug effects
  • Pyridines / pharmacology
  • Signal Transduction / genetics
  • Signal Transduction / physiology
  • Tumor Cells, Cultured
  • Tumor Necrosis Factor-alpha / antagonists & inhibitors
  • Tumor Necrosis Factor-alpha / pharmacology*
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Enzyme Inhibitors
  • I-kappa B Proteins
  • Imidazoles
  • Leupeptins
  • NF-kappa B
  • NFKBIA protein, human
  • Pyridines
  • Tumor Necrosis Factor-alpha
  • Intercellular Adhesion Molecule-1
  • NF-KappaB Inhibitor alpha
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • SB 203580
  • benzyloxycarbonylleucyl-leucyl-leucine aldehyde