4.5 Article

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

期刊

CELLULAR IMMUNOLOGY
卷 266, 期 2, 页码 192-199

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.cellimm.2010.10.005

关键词

Vitamin C; Dendritic cell; Sodium-dependent vitamin C transporter; Th1-shifting; ERK1/2; p38; IL-12p70

资金

  1. Korean Science & Engineering Foundation (KOSEF) through the Tumor Immunity Medical Research Center (TIMRC) at Seoul National University, College of Medicine

向作者/读者索取更多资源

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 naive T cells to secrete more Th1 cytokine, IFN-gamma, 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 1L-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. (C) 2010 Elsevier Inc. All rights reserved.

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