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Effects of the medicinal herb, Panax notoginseng, on the fate and function of professional antigen presenting cells.

机译:三七药对专业抗原呈递细胞的命运和功能的影响。

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摘要

Antigen presenting cells (APCs) perform the essential task of integrating responses between the innate and adaptive immune system. Several approaches have been undertaken to manipulate the effects of APCs for therapeutic purposes. Panax notoginseng is a medicinal herb that is purported to possess a number of properties including modulation of the immune system. However, limited information exists on the effects and toxicities of this herbal on APCs. In this regard, we assessed the effects of Panax notoginseng on the fate and function of professional APCs in murine models using macrophages and dendritic cells (DCs). APCs were stimulated with the toll-like receptor ligands LPS, CpG and poly(I:C) and treated with notoginseng (0-200 mug/ml). The LPS induced levels of the proinflammatory cytokine TNF-alpha, as well as the expression of accessory molecules MHC II, CD40 and CD86, were decreased dependent on notoginseng exposure time-points relative to LPS stimulation. LPS induced IL-1beta, IL-6 and IL-12 production was also decreased with concurrent notoginseng treatment for 24 hours. Notoginseng decreased TNF-alpha and CD40 activation by CpG and poly(I:C), but had varied effects on the induction of IL-6 and CD86. Furthermore, treatment of APCs with ginsenosides Rb1 and Rg1 had differential effects on the production of TNF-alpha and IL-6. Phagocytosis of FITC-conjugated ovalbumin antigen by DCs was decreased by notoginseng. Furthermore, the uptake of FITC-conjugated modified LDL was reduced in notoginseng treated DCs. However, T cell proliferation in response to notoginseng-treated-antigen-loaded DCs was not affected in vitro or in vivo. Mechanistically, notoginseng reduced nuclear levels of the transcription factor NFkappaB, but had no effect on glucocorticoid receptor activation. No immunotoxicities were observed with low dose notoginseng (660 mug/kg) treatment of Balb/c mice in vivo . Collectively, our results indicate that notoginseng decreased inflammatory mediator production by APCs, without altering their ability to induce antigen specific CD 4+ T cell proliferation. Our research provides insight into the potential use of this herbal in the treatment of inflammatory diseases as a safe and effective complement to existing remedies.
机译:抗原呈递细胞(APC)执行整合先天性和适应性免疫系统之间反应的基本任务。为了治疗目的,已经采取了几种方法来操纵APC的作用。三七是一种药用草药,据称具有多种特性,包括调节免疫系统。但是,关于这种草药对APC的作用和毒性的信息有限。在这方面,我们评估了三七对使用巨噬细胞和树突状细胞(DC)的鼠模型中专业APC的命运和功能的影响。用收费型受体配体LPS,CpG和poly(I:C)刺激APC,并用三七(0-200杯/毫升)处理。 LPS诱导的促炎细胞因子TNF-α水平以及辅助分子MHC II,CD40和CD86的表达相对于LPS刺激依赖于三七暴露时间点而降低。 LPS诱导的IL-1β,IL-6和IL-12的产生在同时使用三七处理24小时后也降低了。三七能降低CpG和poly(I:C)对TNF-α和CD40的激活,但对IL-6和CD86的诱导具有不同的作用。此外,用人参皂苷Rb1和Rg1处理APC对TNF-α和IL-6的产生具有不同的影响。三七能减少DC对FITC结合的卵清蛋白抗原的吞噬作用。此外,在三七处理的DC中,FITC缀合的修饰的LDL的摄取减少。然而,在体外或体内,响应于三七处理过的抗原的DCs的T细胞增殖均未受到影响。从机制上讲,三七可以降低转录因子NFkappaB的核水平,但对糖皮质激素受体的激活没有影响。低剂量三七(660杯/千克)在体内治疗Balb / c小鼠时未观察到免疫毒性。总的来说,我们的结果表明三七能降低APC的炎症介质产生,而不会改变它们诱导抗原特异性CD 4+ T细胞增殖的能力。我们的研究提供了对这种草药作为治疗现有疾病的安全有效补充的炎性疾病的潜在用途的见解。

著录项

  • 作者

    Rhule, Ava-Gaye Tania.;

  • 作者单位

    University of Montana.;

  • 授予单位 University of Montana.;
  • 学科 Health Sciences Pharmacology.;Health Sciences Immunology.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 169 p.
  • 总页数 169
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;预防医学、卫生学;
  • 关键词

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