Abstract
Interleukin (IL)-21 is a γc-dependent cytokine produced by activated T cells with important actions for T, B, and NK cells. The IL-21 gene is adjacent to the IL-2 gene, and like IL-2, IL-21 is strongly induced at the transcriptional level after T cell activation. Interestingly, however, in contrast to the IL-2 gene, a calcium ionophore alone was sufficient to induce IL-21 gene expression in preactivated T cells. Two DNase I hypersensitivity sites were found in the IL-21 gene, corresponding to nucleotide sequences that are conserved in humans and mice. One site is located at the IL-21 promoter region and conferred T cell receptor-mediated IL-21 gene transcription. TCR-induced IL-21 gene expression was inhibited by cyclosporin A and FK506. Correspondingly, the IL-21 5′-regulatory region contains three NFAT binding sites, and induction of IL-21 promoter activity was impaired when these sites were mutated or following treatment with cyclosporin A. Thus, our studies reveal that in contrast to IL-2, a calcium signal alone is sufficient to mediate induction of the IL-21 in preactivated T lymphocytes and that this induction appears to result from specific NFAT binding.
Original language | English |
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Pages (from-to) | 25291-25297 |
Number of pages | 7 |
Journal | Journal of Biological Chemistry |
Volume | 280 |
Issue number | 26 |
DOIs | |
State | Published - Jul 1 2005 |
Keywords
- Animals
- Base Sequence
- Binding Sites
- CD4 Antigens/biosynthesis
- Calcium/metabolism
- Cell Line, Tumor
- Chromatin Immunoprecipitation
- Cyclosporine/metabolism
- DNA-Binding Proteins/metabolism
- Deoxyribonuclease I/metabolism
- Gene Expression Regulation
- Humans
- Immunosuppressive Agents/pharmacology
- Interleukin-2/metabolism
- Interleukins/biosynthesis
- Ionophores/metabolism
- Luciferases/metabolism
- Mice
- Mice, Inbred C57BL
- Mice, Knockout
- Models, Genetic
- Molecular Sequence Data
- NFATC Transcription Factors
- Nuclear Proteins/metabolism
- Promoter Regions, Genetic
- Protein Binding
- RNA/metabolism
- Receptors, Antigen, T-Cell/metabolism
- Reverse Transcriptase Polymerase Chain Reaction
- Sequence Homology, Nucleic Acid
- Species Specificity
- T-Lymphocytes/metabolism
- Tacrolimus/pharmacology
- Transcription Factors/metabolism
- Transcription, Genetic