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Metabolic sialic acid blockade lowers the activation threshold of moDCs for TLR stimulation

机译:代谢唾液酸阻断降低了用于TLR刺激的MODC的激活阈值

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摘要

Sialic acid sugars cover the surface of dendritic cells (DCs) and have been suggested to impact several aspects of DC biology. Research into the role of sialic acids in DCs, however, is complicated by the limited number of tools available to modulate sialic acid expression. Here we report on a synthetic, fluorinated sialic acid mimetic, Ac(5)3F(ax)Neu5Ac, which potently blocks sialic acid expression in human monocyte-derived DCs (moDCs). Sialic acid blockade enhanced the responsiveness of moDCs to Toll-like receptor (TLR) stimulation as measured by increased maturation marker expression and cytokine production. Consequently, the T-cell activation capacity of Ac(5)3F(ax)Neu5Ac-treated moDCs was strongly increased. In addition to sialic acids, moDCs also expressed the sialic acid-binding immunoglobulin-like lectins (Siglecs) -3, -5, -7, -9 and -10, immune inhibitory receptors recognizing these sialic acids. Treatment with Ac(5)3F(ax)Neu5Ac abrogated putative cis and trans interactions between sialic acids and Siglec-7/-9. Together, these data indicate that sialic acids limit the activation of moDCs via the TLR pathway, potentially by interacting with Siglec-7 or Siglec-9. Metabolic sialic acid blockade with Ac(5)3F(ax)Neu5Ac could therefore potentially be used to generate more potent DC-based vaccines for induction of robust anti-viral or anti-tumor immune responses.
机译:唾液酸糖覆盖树突细胞(DCS)的表面,并提出了影响DC生物学的若干方面。然而,通过可用于调节唾液酸表达的有限工具,唾液酸在DCS中的作用是复杂的。在这里,我们报告了合成,氟化唾液酸模拟物,AC(5)3F(AX)Neu5ac,其易于阻断人单核细胞衍生的DCS(MODC)中的唾液酸表达。唾液酸阻断增强了ModCs对Toll样受体(TLR)刺激的反应性,通过增加成熟标记表达和细胞因子产生来测量。因此,强烈增加了AC(5)3F(AX)Neu5Ac处理的MODC的T细胞活化能力。除了唾液酸外,MODC还表达了鉴定这些唾液酸的免疫抑制剂的唾液酸结合免疫球蛋白样凝集素(Siglecs)-3,-5,-7,-9和-10。用AC(5)3F(AX)NEU5AC废弃调用的顺式和唾液酸和SIGLEC-7 / -9之间的反相载体处理。这些数据在一起表明,唾液酸通过TLR途径限制了MODC的激活,可能通过与SIGLEC-7或SIGLEC-9相互作用。因此,具有AC(5)3F(AX)NEU5AC的代谢唾液酸阻断可能用于产生更有效的基于DC的疫苗,用于诱导鲁棒抗病毒或抗肿瘤免疫应答。

著录项

  • 来源
    《Immunology and Cell Biology》 |2017年第4期|共8页
  • 作者单位

    Radboud Univ Nijmegen Med Ctr Radboud Inst Mol Life Sci Dept Tumor Immunol Geert Grootepl 28;

    Radboud Univ Nijmegen Med Ctr Radboud Inst Mol Life Sci Dept Tumor Immunol Geert Grootepl 28;

    Radboud Univ Nijmegen Med Ctr Radboud Inst Mol Life Sci Dept Tumor Immunol Geert Grootepl 28;

    Radboud Univ Nijmegen Inst Mol &

    Mat Cluster Mol Chem Nijmegen Netherlands;

    Radboud Univ Nijmegen Med Ctr Radboud Inst Mol Life Sci Dept Tumor Immunol Geert Grootepl 28;

    Radboud Univ Nijmegen Med Ctr Radboud Inst Mol Life Sci Dept Tumor Immunol Geert Grootepl 28;

    Radboud Univ Nijmegen Med Ctr Radboud Inst Mol Life Sci Dept Tumor Immunol Geert Grootepl 28;

    Radboud Univ Nijmegen Inst Mol &

    Mat Cluster Mol Chem Nijmegen Netherlands;

    Radboud Univ Nijmegen Med Ctr Radboud Inst Mol Life Sci Dept Tumor Immunol Geert Grootepl 28;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 医学免疫学;
  • 关键词

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