• Title of article

    Vitamin C-treated murine bone marrow-derived dendritic cells preferentially drive naïve T cells into Th1 cells by increased IL-12 secretions

  • Author/Authors

    Jeong، نويسنده , , Young-Joo and Hong، نويسنده , , Seung-Woo and Kim، نويسنده , , Jin-Hee and Jin، نويسنده , , Dong-Hoon and Kang، نويسنده , , Jae-Seung and Lee، نويسنده , , Wang Jae and Hwang، نويسنده , , Young-il، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2011
  • Pages
    8
  • From page
    192
  • To page
    199
  • Abstract
    Vitamin C has been reported to shift immune responses toward Th1. In this study, we evaluated whether this effect was by way of dendritic cells. Murine dendritic cells (DCs) were prepared from bone marrow precursors. DCs treated with vitamin C secreted an increased amount of IL-12p70 after activation with LPS. These cells rendered naïve T cells to secrete more Th1 cytokine, IFN-γ, and less Th2-cytokine, IL-5 in the culture supernatants. Vitamin C-treatment also increased phosphorylation of p38 and ERK1/2 in DCs. p38 inhibitor in culture media suppressed the effect of vitamin C to elevate IL-12p70 secretion. In contrast, ERK inhibitor elevated IL-12p70 secretion. In summary, vitamin C taken up into DCs increased IL-12p70 secretion of these cells by modulating the activation of signal molecules, and thus shifted immune responses toward Th1. These data provide us a new insight on the role of vitamin C in modulating immune responses.
  • Keywords
    dendritic cell , Sodium-dependent vitamin C transporter , Th1-shifting , P38 , IL-12p70 , Vitamin C , ERK1/2
  • Journal title
    Cellular Immunology
  • Serial Year
    2011
  • Journal title
    Cellular Immunology
  • Record number

    1861301