• Title of article

    TLR4-independent and PKR-dependent interleukin 1 receptor antagonist expression upon LPS stimulation

  • Author/Authors

    Na، نويسنده , , Hye Young and Mazumdar، نويسنده , , Kaushiki and Moon، نويسنده , , Hye-Jung and Chang، نويسنده , , Sooghee and Seong، نويسنده , , Seung-Yong، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2009
  • Pages
    8
  • From page
    33
  • To page
    40
  • Abstract
    Dendritic cells (DCs) induce innate immune responses by recognizing bacterial LPS through TLR4 receptor complexes. In this study, we compared gene expression profiles of TLR4 knockout (TLR4neg) DCs and wild type (TLR4pos) DCs after stimulating with LPS. We found that the expression of various inflammatory genes by LPS were TLR4-independent. Among them, interleukin 1 receptor antagonist (IL-1rn) was of particular interest since IL-1rn is a potent natural inhibitor of proinflammatory IL-1. Using RT-PCR, real-time PCR, immunoblotting and ELISA, we demonstrated that IL-1rn was induced by DCs stimulated with LPS in the absence of TLR4. 2-Aminopurine, a pharmacological PKR inhibitor, completely abrogated LPS-induced expression of IL-1rn in TLR4neg DCs, suggesting that LPS-induced TLR4-independent expression of IL-1rn might be mediated by PKR pathways. Considering that IL-1rn is a physiological inhibitor of IL-1, TLR4-independent and PKR-dependent pathways might be crucial in counter-balancing proinflammatory effector functions of DCs resulted from TLR4-dependent activation by LPS.
  • Keywords
    PKR , LPS , Sepsis , TLR4 , IL-1RN
  • Journal title
    Cellular Immunology
  • Serial Year
    2009
  • Journal title
    Cellular Immunology
  • Record number

    1860601