Constitutive expression of IL-18 and IL-18R in differentiated IEC-6 cells: effect of TNF-alpha and IFN-gamma treatment
Language English Country United States Media print
Document type Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't
Grant support
HD-47237
NICHD NIH HHS - United States
PubMed
18547159
DOI
10.1089/jir.2006.0130
Knihovny.cz E-resources
- MeSH
- Apoptosis drug effects MeSH
- Biomarkers metabolism MeSH
- Cell Differentiation drug effects MeSH
- Cell Membrane drug effects metabolism MeSH
- Cell Line MeSH
- Chemokine CCL2 metabolism MeSH
- Epithelial Cells cytology drug effects enzymology metabolism MeSH
- Interferon-gamma pharmacology MeSH
- Interleukin-18 genetics metabolism MeSH
- Caspase 1 metabolism MeSH
- Rats MeSH
- Culture Media MeSH
- RNA, Messenger genetics metabolism MeSH
- Cell Count MeSH
- Reverse Transcriptase Polymerase Chain Reaction MeSH
- Interleukin-18 Receptor alpha Subunit genetics metabolism MeSH
- Interleukin-18 Receptor beta Subunit genetics metabolism MeSH
- Gene Expression Regulation drug effects MeSH
- Intestines cytology MeSH
- Tumor Necrosis Factor-alpha pharmacology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, N.I.H., Extramural MeSH
- Names of Substances
- Biomarkers MeSH
- Chemokine CCL2 MeSH
- Interferon-gamma MeSH
- Interleukin-18 MeSH
- Caspase 1 MeSH
- Culture Media MeSH
- RNA, Messenger MeSH
- Interleukin-18 Receptor alpha Subunit MeSH
- Interleukin-18 Receptor beta Subunit MeSH
- Tumor Necrosis Factor-alpha MeSH
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.
References provided by Crossref.org