Constitutive expression of IL-18 and IL-18R in differentiated IEC-6 cells: effect of TNF-alpha and IFN-gamma treatment

J Interferon Cytokine Res. 2008 May;28(5):287-96. doi: 10.1089/jir.2006.0130.

Abstract

The multifunctional cytokine interleukin-18 (IL-18) is an important mediator in intestinal inflammatory processes. The aim of this study was to evaluate the constitutive expression of IL-18 and its receptors (IL-18Ralpha and IL-18Rbeta) in intestinal epithelial cells (IEC) stimulated by tumor necrosis factor-alpha (TNF-alpha) and interferon-gamma (IFN-gamma). In addition, cellular proliferation and evaluation of brush border enzymes as differentiation markers were studied. Nontransformed rat intestinal epithelial IEC-6 cells were grown on an extracellular matrix (ECM) in medium with or without TNF-alpha, IFN-gamma, or a combination of both. Gene expression of IL-18, its receptors and apoptotic markers was evaluated using real-time PCR. Expression of IL-18Ralpha protein was demonstrated by flow cytometry and Western blot. Enzymatic activities of brush border enzymes and caspase-1 were determined. The constitutive expression of IL-18, IL-18Ralpha and IL-18Rbeta mRNAs and proteins were detected in IEC-6 cells. The biologically active form of IL-18 was released in response to TNF-alpha and IFN-gamma treatment. Exogenous IL-18 had no effect on cellular proliferation, brush border enzyme activities, and gene expression of apoptotic markers. However, the addition of IL-18 stimulated production and release of the chemokine IL-8. These data suggest that IEC-6 cells may be not only a source of IL-18 but also a target for its action.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Biomarkers / metabolism
  • Caspase 1 / metabolism
  • Cell Count
  • Cell Differentiation / drug effects*
  • Cell Line
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Chemokine CCL2 / metabolism
  • Culture Media
  • Epithelial Cells / cytology*
  • Epithelial Cells / drug effects
  • Epithelial Cells / enzymology
  • Epithelial Cells / metabolism
  • Gene Expression Regulation / drug effects
  • Interferon-gamma / pharmacology*
  • Interleukin-18 / genetics*
  • Interleukin-18 / metabolism
  • Interleukin-18 Receptor alpha Subunit / genetics*
  • Interleukin-18 Receptor alpha Subunit / metabolism
  • Interleukin-18 Receptor beta Subunit / genetics*
  • Interleukin-18 Receptor beta Subunit / metabolism
  • Intestines / cytology
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • Biomarkers
  • Chemokine CCL2
  • Culture Media
  • Interleukin-18
  • Interleukin-18 Receptor alpha Subunit
  • Interleukin-18 Receptor beta Subunit
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma
  • Caspase 1