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Constitutive expression of IL-18 and IL-18R in differentiated IEC-6 cells: effect of TNF-alpha and IFN-gamma treatment
J. Kolínská, V. Lisá, J.A. Clark, H. Kozáková, M. Zákostelecká, L. Khailová, M. Šinkora, A. Kitanovičová, B. Dvořák
Jazyk angličtina Země Spojené státy americké
NLK
ProQuest Central
od 1998-10-01 do 2018-12-31
Health & Medicine (ProQuest)
od 1998-10-01 do 2018-12-31
Public Health Database (ProQuest)
od 1998-10-01 do 2018-12-31
PubMed
18547159
DOI
10.1089/jir.2006.0130
Knihovny.cz E-zdroje
- MeSH
- apoptóza účinky léků MeSH
- biologické markery metabolismus MeSH
- buněčná diferenciace účinky léků MeSH
- buněčná membrána metabolismus účinky léků MeSH
- buněčné linie MeSH
- chemokin CCL2 metabolismus MeSH
- epitelové buňky MeSH
- financování organizované MeSH
- interferon gama farmakologie MeSH
- interleukin-18 genetika sekrece MeSH
- kaspasa 1 metabolismus MeSH
- krysa rodu rattus MeSH
- kultivační média MeSH
- messenger RNA genetika metabolismus MeSH
- počet buněk MeSH
- polymerázová řetězová reakce s reverzní transkripcí MeSH
- receptor interleukinu-18 - alfa-podjednotka genetika metabolismus MeSH
- receptor interleukinu-18 - beta-podjednotka genetika metabolismus MeSH
- regulace genové exprese účinky léků MeSH
- střeva cytologie MeSH
- TNF-alfa farmakologie MeSH
- zvířata MeSH
- Check Tag
- krysa rodu rattus MeSH
- zvířata 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.
Citace poskytuje Crossref.org
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