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    Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/50822


    Title: GM-CSF plays a key role in zymosan-stimulated human dendritic cells for activation of Th1 and Th17 cells
    Authors: Wei,WC;Su,YH;Chen,SS;Sheu,JH;Yang,NS
    Contributors: 生命科學系
    Keywords: TUMOR-NECROSIS-FACTOR;CANCER-IMMUNOTHERAPY;IMMUNOLOGICAL-TOLERANCE;IMMUNE-RESPONSE;T-CELLS;INFLAMMATION;DECTIN-1;VACCINE;INTERLEUKIN-12;PROMOTES
    Date: 2011
    Issue Date: 2012-03-27 18:10:44 (UTC+8)
    Publisher: 國立中央大學
    Abstract: In this study, we compared the effects of zymosan and LPS on human monocyte-derived dendritic cells. The specific effects of zymosan on the expression of several key cytokines, including granulocyte-macrophage colony-stimulating factor (GM-CSF) and interleukins (IL-1 alpha, IL-1 beta and IL-12 p70) were quite distinct from the effects of LPS. Unlike activation with LPS, DCs activated by zymosan expressed little or no IL-12 p70 due to lack of expression of the p35 subunit. However, treatment with zymosan resulted in a substantial increase in Th1 and Th17 cell-polarizing capacity of DCs. Furthermore, the GM-CSF secreted by zymosan-activated DCs enhanced IL-23 production, resulting in activation of a Th17 response. GM-CSF and IL-27, rather than IL-12 p70, were both major direct contributors to the activation of a Th1 response. This signaling mechanism is distinct and yet complementary to LPS-mediated T-cell activation. We suggest that this novel zymosan-induced GM-CSF-mediated signaling network may play a key role in regulating specific immune cell type activities. (C) 2011 Elsevier Ltd. All rights reserved.
    Relation: CYTOKINE
    Appears in Collections:[Department of Life Science] journal & Dissertation

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