Fractalkine-mediated signals regulate cell-survival and immune-modulatory responses in intestinal epithelial cells

Gastroenterology. 2002 Jan;122(1):166-77. doi: 10.1053/gast.2002.30329.

Abstract

Background & aims: In this study, we determined the signal transduction and functional consequences after ligand-specific activation of the fractalkine receptor CX3CR1 in human intestinal epithelial cells.

Methods: CX3CR1 expression in human colonic tissues and intestinal epithelial cell lines was determined by immunohistochemistry, immunoblotting, and reverse-transcription polymerase chain reaction. The regulation of mitogen-activated protein kinase (MAPK) activation was assessed by immunoblotting. Regulation of chemokine messenger RNA (mRNA) expression was determined by Northern blotting. NF-kappa B and p53 activation was assessed by electromobility shift assays.

Results: Fractalkine mediated the MEK-1 and G alpha i-dependent but phosphatidylinositol-3-kinase-independent activation of extracellular signal-regulated kinase-MAPK. Fractalkine activated NF-kappa B and p53 resulting in interleukin 8 and fractalkine mRNA expression. CX3CR1-mediated activation of intestinal epithelial cells was able to induce migration of human neutrophils into but not through the intestinal epithelial cell monolayer.

Conclusions: CX3CR1 mediates distinct functional responses in intestinal epithelial cells, which include the autocrine regulation of cell-survival signals and activation of immune modulators, indicating a role of CX3CR1 in host defense mechanisms originating from the intestinal epithelium.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adjuvants, Immunologic / metabolism*
  • Autocrine Communication / immunology
  • CX3C Chemokine Receptor 1
  • Caco-2 Cells
  • Cell Division / physiology
  • Cell Membrane / metabolism
  • Cell Nucleus / metabolism
  • Cell Survival / physiology
  • GTP-Binding Protein alpha Subunits, Gi-Go / metabolism
  • Gene Expression / physiology
  • Humans
  • Intestinal Mucosa / cytology
  • Intestinal Mucosa / immunology
  • Intestinal Mucosa / metabolism*
  • MAP Kinase Kinase 1
  • MAP Kinase Signaling System / immunology*
  • Mitogen-Activated Protein Kinase 1 / metabolism
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinase Kinases / metabolism
  • Mitogen-Activated Protein Kinases / metabolism
  • NF-kappa B / metabolism
  • Neutrophils / cytology
  • Phosphatidylinositol 3-Kinases / metabolism
  • Protein Serine-Threonine Kinases / metabolism
  • Receptors, Cytokine / genetics*
  • Receptors, Cytokine / immunology
  • Receptors, Cytokine / metabolism*
  • Receptors, HIV / genetics*
  • Receptors, HIV / immunology
  • Receptors, HIV / metabolism*
  • Stomach Neoplasms
  • Tumor Suppressor Protein p53 / metabolism

Substances

  • Adjuvants, Immunologic
  • CX3C Chemokine Receptor 1
  • NF-kappa B
  • Receptors, Cytokine
  • Receptors, HIV
  • Tumor Suppressor Protein p53
  • Protein Serine-Threonine Kinases
  • Mitogen-Activated Protein Kinase 1
  • Mitogen-Activated Protein Kinase 3
  • Mitogen-Activated Protein Kinases
  • MAP Kinase Kinase 1
  • MAP2K1 protein, human
  • Mitogen-Activated Protein Kinase Kinases
  • GTP-Binding Protein alpha Subunits, Gi-Go