文化大學機構典藏 CCUR:Item 987654321/36135
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    Please use this identifier to cite or link to this item: https://irlib.pccu.edu.tw/handle/987654321/36135


    Title: Glossogyne tenuifolia (Hsiang-ju) extract suppresses T cell activation by inhibiting activation of c-Jun N-terminal kinase
    Authors: Houng, JY (Houng, Jer-Yiing)
    Tai, TS (Tai, Tzong-Shyuan)
    Hsu, SC (Hsu, Shu-Ching)
    Hsu, HF (Hsu, Hsia-Fen)
    Hwang, TS (Hwang, Tzann-Shun)
    Lin, CJ (Lin, Chih-Jiun)
    Fang, LW (Fang, Li-Wen)
    Contributors: 生科所
    Keywords: KAPPA-B
    CANCER-IMMUNOTHERAPY
    ANTIOXIDANT ACTIVITY
    DEATH
    LYMPHOCYTES
    APOPTOSIS
    PROLIFERATION
    JNK
    CTL
    EXPRESSION
    Date: 2017-04
    Issue Date: 2017-06-08 11:05:12 (UTC+8)
    Abstract: Background: Glossogyne tenuifolia (GT) (Hsiang-ju) is a Chinese herbal medicine previously exhibited an anti-inflammatory activity. This study aimed to investigate the effect of GT ethanol extract (GTE) on T cell-mediated adaptive immunity.

    Methods: Human peripheral blood mononuclear cells (PBMCs) and Jurkat T cells were activated by phytohemagglutinin in the presence of various doses (3.13-50 mu g/mL) of GTE. The effect of GTE on T cell activation was examined by a proliferation assay of activated PBMCs and the level of the activation marker CD69 on the surface of activated Jurkat T cells. Apoptosis was determined by propidium iodide staining in hypotonic solution. Signaling pathway molecules were assessed by western blotting.

    Results: Glossogyne tenuifolia ethanol extract was demonstrated to inhibit T cell activation, not only in the proliferation of human PBMCs at the concentrations of 12.5, 25 and 50 mu g/mL (P = 0.0118, 0.0030 and 0.0021) but also in the CD69 expression in Jurkat cells, which was not due to the cytotoxicity of GTE. The presence of GTE did not change the activity of nuclear factor kappa-light-chain-enhancer of activated B cells or extracellular signal-regulated kinase upon T cell activation. In addition, GTE significantly reduced activation of c-Jun N-terminal kinase (JNK) (P = 0.0167) and p38 (P = 0.0278). Furthermore, decreased JNK activation mediated the preventive effect of GTE on T cell activation-induced cell death (AICD).

    Conclusion: Glossogyne tenuifolia ethanol extract inhibited T cell activation of Jurkat cells and freshly prepared human PBMCs due to suppression of JNK activity. Furthermore, GTE inhibited AICD by blocking prolonged JNK phosphorylation in activated T cells. Taken together, the anti-inflammatory effects exerted by GTE were mediated via suppression of JNK phosphorylation in T cell activation.
    Relation: CHINESE MEDICINE 卷: 12 文獻號碼: 9
    Appears in Collections:[Graduate Institute of Biotechnology ] journal articles

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