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

  1. Author:
    Kim, H. P.
    Korn, L. L.
    Gamero, A. M.
    Leonard, W. J.
  2. Author Address

    NHLBI, Lab Mol Immunol, NIH, Bethesda, MD 20892 USA. NCI, Expt Immunol Lab, NIH, Frederick, MD 21702 USA Leonard, WJ, NHLBI, Lab Mol Immunol, NIH, Bldg 10,Rm 7N252, Bethesda, MD 20892 USA
    1. Year: 2005
    2. Date: JUL 1
  1. Journal: Journal of Biological Chemistry
    1. 280
    2. 26
    3. Pages: 25291-25297
  2. Type of Article: Article
  1. Abstract:

    Interleukin (IL)-21 is a gamma(c)-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

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External Sources

  1. WOS: 000230114000116

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