Selective eosinophil adhesion to fibroblast via IFN-gamma-induced galectin-9

J Immunol. 2002 Nov 15;169(10):5912-8. doi: 10.4049/jimmunol.169.10.5912.

Abstract

Among galectin family members, galectin-9 was first described as a potent eosinophil chemoattractant derived from Ag-stimulated T cells. In the present study a role of galectin-9 in the interaction between eosinophils and fibroblasts was investigated using a human lung fibroblast cell line, HFL-1. RT-PCR, real-time PCR, and Western blot analyses revealed that both galectin-9 mRNA and protein in HFL-1 cells were up-regulated by IFN-gamma stimulation. On the one hand, IL-4, known as a Th2 cytokine, did not affect the galectin-9 expression in HFL-1 cells. We further confirmed that IFN-gamma up-regulated the expression of galectin-9 in primary human dermal fibroblasts. Flow cytometric analysis revealed that IFN-gamma up-regulated surface galectin-9 expression on HFL-1 cells. Stimulation of HFL-1 cells with IFN-gamma up-regulated adhesion of eosinophils, but not neutrophils, to HFL-1 cells. This adherence of eosinophils to HFL-1 cells was inhibited by both lactose and anti-galectin-9 Ab. These findings demonstrate that IFN-gamma-induced galectin-9 expression in fibroblasts mediates eosinophil adhesion to the cells, suggesting a crucial role of galectin-9 in IFN-gamma-stimulated fibroblasts as a physiological modulator at the inflammatory sites.

MeSH terms

  • Adult
  • Cell Adhesion / physiology
  • Cell Line
  • Cell-Free System / chemistry
  • Cell-Free System / physiology
  • Chemotactic Factors, Eosinophil / biosynthesis
  • Chemotactic Factors, Eosinophil / isolation & purification
  • Chemotactic Factors, Eosinophil / physiology
  • Eosinophils / physiology*
  • Female
  • Fibroblasts / metabolism
  • Fibroblasts / physiology*
  • Galectins / biosynthesis*
  • Galectins / isolation & purification
  • Galectins / physiology*
  • Humans
  • Interferon-gamma / pharmacology*
  • Lung / metabolism
  • Lung / pathology
  • Lung Diseases, Interstitial / metabolism
  • Lung Diseases, Interstitial / pathology
  • Middle Aged
  • Neutrophils / physiology
  • Pulmonary Eosinophilia / metabolism
  • Pulmonary Eosinophilia / pathology

Substances

  • Chemotactic Factors, Eosinophil
  • Galectins
  • LGALS9 protein, human
  • Interferon-gamma