Calcium-dependent activation of interleukin-21 gene expression in T cells

Hyoung Pyo Kim, Lisa L. Korn, Ana M. Gamero, Warren J. Leonard

Research output: Contribution to journalArticlepeer-review

77 Scopus citations

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 languageEnglish
Pages (from-to)25291-25297
Number of pages7
JournalJournal of Biological Chemistry
Volume280
Issue number26
DOIs
StatePublished - 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

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