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Toll-like receptor triggering of a vitamin D-mediated human antimicrobial response

机译:Toll样受体触发维生素D介导的人类抗菌反应

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摘要

In innate immune responses, activation of Toll-like receptors (TLRs) triggers direct antimicrobial activity against intracellular bacteria, which in murine, but not human, monocytes and macrophages is mediated principally by nitric oxide. We report here that TLR activation of human macrophages up-regulated expression of the vitamin D receptor and the vitamin D-1-hydroxylase genes, leading to induction of the antimicrobial peptide cathelicidin and killing of intracellular Mycobacterium tuberculosis. We also observed that sera from African-American individuals, known to have increased susceptibility to tuberculosis, had low 25-hydroxyvitamin D and were inefficient in supporting cathelicidin messenger RNA induction. These data support a link between TLRs and vitamin D-mediated innate immunity and suggest that differences in ability of human populations to produce vitamin D may contribute to susceptibility to microbial infection.
机译:在先天性免疫应答中,Toll样受体(TLR)的激活触发了针对细胞内细菌的直接抗菌活性,这种细菌在鼠类而非人的单核细胞和巨噬细胞中主要由一氧化氮介导。我们在这里报告,人类巨噬细胞的TLR激活上调了维生素D受体和维生素D-1-羟化酶基因的表达,从而导致抗菌肽cathelicidin的诱导和细胞内结核分枝杆菌的杀伤。我们还观察到来自非裔美国人的血清,已知其对肺结核的敏感性增加,其25-羟基维生素D含量低,并且在支持cathelicidin信使RNA诱导方面效率低下。这些数据支持TLR和维生素D介导的先天免疫之间的联系,并表明人类生产维生素D的能力差异可能会导致对微生物感染的易感性。

著录项

  • 来源
    《Science》 |2006年第5768期|p. 1770-1773|共4页
  • 作者单位

    Univ Calif Los Angeles, Dept Microbiol Mol Genet & Immunol, Los Angeles, CA 90095 USA;

    Univ Calif Los Angeles, David Geffen Sch Med, Dept Med, Div Dermatol, Los Angeles, CA 90095 USA;

    Univ Calif Los Angeles, Howard Hughes Med Inst, Dept Chem & Biol Chem, Los Angeles, CA 90095 USA;

    Univ Calif Los Angeles, Inst Genom & Proteom, Dept Energy, Los Angeles, CA 90095 USA;

    Univ Calif San Diego, Div Dermatol, La Jolla, CA 92161 USA;

    Univ Erlangen Nurnberg, Inst Klin Mikrobiol Immunol & Hyg, D-91054 Erlangen, Germany;

    Vet Affairs San Diego Healthcare Ctr, La Jolla, CA 92161 USA;

    Med Univ S Carolina, Dept Med, Charleston, SC 29425 USA;

    Klinikum Nurnberg, Med Klin 3, D-90340 Nurnberg, Germany;

    Univ Marburg, D-35043 Marburg, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 自然科学总论;
  • 关键词

    NITRIC-OXIDE SYNTHASE; MYCOBACTERIUM-TUBERCULOSIS; SUSCEPTIBILITY; EXPRESSION; INFECTION;

    机译:一氧化氮合酶;结核分枝杆菌;敏感性;表达;感染;
  • 入库时间 2022-08-18 02:56:16

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