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Inflamm Res ; 51(9): 457-63, 2002 Sep.
Article in English | MEDLINE | ID: mdl-12365719

ABSTRACT

OBJECTIVE: Interleukin (IL)-18 is involved in host defense mechanisms and inflammatory diseases, among them rheumatoid arthritis (RA). High levels of IL-18 expression in RA joints are contrasted by reduced IL-18 expression in RA peripheral blood mononuclear cells (PBMC). Here, we investigated a putative IL-18 regulating role of corticosteroids. METHODS: IL-18 transcript and protein levels in PBMC from untreated and prednisolone treated RA patients, and from healthy donors were assessed by semiquantitative reverse transcriptase polymerase chain reaction (RT-PCR) and immunoblotting. IL-18 regulation was determined in PBMC and U937 cells upon exposure to prednisolone in vitro by RT-PCR and Northern Blot analysis, by ELISA in cell culture supernatants, and in transiently transfected THP-1 cells by IL-18 promoter activity luciferase assays. RESULTS: In RA PBMC, IL-18 transcript levels were dose dependently restored, in parallel with administered prednisolone treatment, to subnormal levels. The corresponding intracellular IL-18 deposits in contrast were depleted. In cultured PBMC and promonocytic cell lines, prednisolone up-regulated IL-18 transcription in parallel with increasing the IL- 18 protein release into cell culture supernatants. CONCLUSION: Prednisolone increases IL-18 expression and release in PBMC and monocytic cell lines.


Subject(s)
Arthritis, Rheumatoid/metabolism , Glucocorticoids/pharmacology , Interleukin-18/metabolism , Monocytes/metabolism , Myeloid Progenitor Cells/metabolism , Prednisolone/pharmacology , Adult , Aged , Cells, Cultured , Female , Humans , Interleukin-18/genetics , Male , Middle Aged , Monocytes/drug effects , Myeloid Progenitor Cells/drug effects , RNA, Messenger/metabolism
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