IL-21 up-regulates the expression of genes associated with innate immunity and Th1 response

J Immunol. 2002 Oct 1;169(7):3600-5. doi: 10.4049/jimmunol.169.7.3600.

Abstract

IL-21 is a recently characterized T cell-derived cytokine that regulates NK and T cell function. IL-21R shares the common gamma-chain (gamma(c)) with the receptors for IL-2, IL-4, IL-7, IL-9, and IL-15. Despite the same gamma(c), these cytokines have different effects on diverse cells. In this study, we have studied IL-15- and IL-21-induced gene expression in human primary NK and T cells and the NK-92 cell line. Both IL-15 and IL-21 rapidly induced mRNA synthesis for IFN-gamma, T-bet, IL-2Ralpha, IL-12Rbeta2, IL-18R, and myeloid differentiation factor 88 (MyD88), the genes that are important in activating innate immunity and Th1 response. IL-15 induced STAT5 DNA binding to the IL-2Ralpha IFN-gamma-activated sequence (GAS), MyD88 GAS, and c-cis-inducible elements, whereas IL-21 induced STAT3 DNA binding to MyD88 GAS and c-sis-inducible elements. IL-21-induced STAT3 activation was verified by immunoprecipitation and Western blotting with anti-phosphotyrosine Ab. In addition, pretreatment of NK-92 cells with IL-15 or IL-21 strongly enhanced IL-12-induced STAT4 DNA binding to IL-2Ralpha GAS. The induction of IFN-gamma, T-bet, IL-12Rbeta2, and IL-18R gene expression in NK cells, along with STAT3 activation, suggests that IL-21 is involved in the activation of innate immune responses. Moreover, the enhanced transcription of these genes in T cells establishes a significant role for IL-21 also in the Th1 response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Antigens, Differentiation / metabolism
  • Cells, Cultured
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation / immunology*
  • Humans
  • Immunity, Innate / genetics*
  • Interferon Regulatory Factor-1
  • Interleukin-15 / pharmacology
  • Interleukins / pharmacology
  • Interleukins / physiology*
  • Janus Kinase 1
  • Janus Kinase 3
  • Killer Cells, Natural / metabolism
  • Lymphocyte Activation / genetics
  • Lymphocyte Activation / immunology
  • Milk Proteins*
  • Myeloid Differentiation Factor 88
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Protein Binding / immunology
  • Protein-Tyrosine Kinases / metabolism
  • Receptors, Immunologic / metabolism
  • Response Elements / immunology
  • STAT1 Transcription Factor
  • STAT3 Transcription Factor
  • STAT5 Transcription Factor
  • T-Box Domain Proteins
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism
  • Th1 Cells / immunology*
  • Th1 Cells / metabolism
  • Trans-Activators / metabolism
  • Transcription Factors / metabolism
  • Tyrosine / metabolism
  • Up-Regulation / genetics*
  • Up-Regulation / immunology*

Substances

  • Adaptor Proteins, Signal Transducing
  • Antigens, Differentiation
  • DNA-Binding Proteins
  • IRF1 protein, human
  • Interferon Regulatory Factor-1
  • Interleukin-15
  • Interleukins
  • MYD88 protein, human
  • Milk Proteins
  • Myeloid Differentiation Factor 88
  • Phosphoproteins
  • Receptors, Immunologic
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT3 Transcription Factor
  • STAT3 protein, human
  • STAT5 Transcription Factor
  • T-Box Domain Proteins
  • T-box transcription factor TBX21
  • Trans-Activators
  • Transcription Factors
  • Tyrosine
  • Protein-Tyrosine Kinases
  • JAK1 protein, human
  • JAK3 protein, human
  • Janus Kinase 1
  • Janus Kinase 3
  • interleukin-21