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IL-18-stimulated GADD45 beta required in cytokine-induced, but not TCR-induced, IFN-gamma production.
- Source :
-
Nature immunology [Nat Immunol] 2001 Feb; Vol. 2 (2), pp. 157-64. - Publication Year :
- 2001
-
Abstract
- Interleukin-12 (IL-12) and IL-18 induce synergistic transcription of interferon gamma (IFN-gamma) that is T cell receptor (TCR)-independent, not inhibited by cyclosporin A and requires new protein synthesis. To characterize this pathway, we screened for genes that are induced in IL-12- and IL-18-treated T helper type 1 cells. GADD45 beta, which activates mitogen-activated protein kinase (MAPK)-extracellular signal-regulated kinase kinase 4 (MEKK4), was induced by IL-18 and augmented by IL-12. GADD45 beta expression in naïve CD4+ T cells activated p38 MAPK and selectively increased cytokine-induced, but not TCR-induced, IFN-gamma production. Kinase-inactive MEKK4 and inhibition of the p38 MAPK pathway both selectively inhibit cytokine-induced, but not TCR-induced, IFN-gamma production. Thus, the synergy between IL-12 and IL-18 may involve GADD45 beta induction, which can maintain the MEKK4 and p38 MAPK activation that is necessary for cytokine-induced, but not TCR-induced, IFN-gamma production.
- Subjects :
- Animals
Base Sequence
Cell Line
Cytokines pharmacology
DNA Primers genetics
Humans
Interleukin-12 pharmacology
Intracellular Signaling Peptides and Proteins
MAP Kinase Kinase Kinase 4
MAP Kinase Kinase Kinases genetics
MAP Kinase Kinase Kinases metabolism
Mice
Mice, Transgenic
Mitogen-Activated Protein Kinases metabolism
Protein Biosynthesis
Proteins genetics
Receptors, Antigen, T-Cell metabolism
T-Lymphocytes drug effects
T-Lymphocytes immunology
T-Lymphocytes metabolism
p38 Mitogen-Activated Protein Kinases
GADD45 Proteins
Interferon-gamma biosynthesis
Interleukin-18 pharmacology
Proteins metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1529-2908
- Volume :
- 2
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Nature immunology
- Publication Type :
- Academic Journal
- Accession number :
- 11175814
- Full Text :
- https://doi.org/10.1038/84264