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Dermal tumour necrosis factor-alpha induces dendritic cell migration to draining lymph nodes and possibly provides one stimulus for Langerhans cell migration.

机译:皮肤肿瘤坏死因子-α诱导树突状细胞迁移至引流淋巴结并可能为朗格汉斯细胞迁移提供一种刺激。

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摘要

Previous studies have shown that following skin sensitization there is an accumulation of dendritic cells (DC) in lymph nodes draining the site of exposure. A significant number of the DC which arrive in the lymph nodes bear high levels of antigen, and the available evidence indicates that they are derived from epidermal Langerhans' cells (LC). Although freshly isolated LC are relatively inefficient antigen-presenting cells, the antigen-bearing DC which are found within draining nodes following skin sensitization are highly immunostimulatory. Recent investigations indicate that the functional maturation of LC as they migrate from the skin is reflected by an enhanced capacity to form stable clusters with lymphocytes, and is associated with an increased expression of membrane major histocompatibility complex (MHC) class II (Ia) antigen. By analogy with in vitro studies of LC maturation, it is possible that such changes are effected by granulocyte/macrophage colony-stimulating factor (GM-CSF) and interleukin-1 (IL-1), both of which are products of epidermal cells. The question remains as to the nature of the stimulus that initiates LC migration. In the present study we have examined in mice the effects of intradermal injection of tumour necrosis factor-alpha (TNF-alpha), another epidermal cytokine, on the accumulation of DC in lymph nodes. Murine recombinant TNF-alpha was found to cause a concentration- and time-dependent increase in the number of DC within draining nodes. Under the same conditions of exposure murine recombinant GM-CSF was without effect. Heat treatment of mouse TNF-alpha resulted in an equivalent inhibition of both DC accumulation and cytotoxic activity measured by in vitro bioassay. An interesting observation was that equal concentrations of human TNF-alpha, of equivalent specific activity, failed to influence the frequency of lymph node DC. These data demonstrate that TNF-alpha induces DC accumulation in draining lymph nodes, and we propose that this cytokine may provide one stimulus for LC migration during cutaneous immune responses.
机译:先前的研究表明,在皮肤致敏后,淋巴结中有树突状细胞(DC)积聚,流失了暴露部位。到达淋巴结的大量DC含有高水平的抗原,现有证据表明它们源自表皮朗格汉斯细胞(LC)。尽管新鲜分离的LC是效率相对较低的抗原呈递细胞,但是在皮肤致敏后在引流节点内发现的带有抗原的DC具有高度的免疫刺激性。最近的研究表明,当LC从皮肤迁移时,其功能成熟与淋巴细胞形成稳定簇的能力增强有关,并且与膜主要组织相容性复合物(MHC)II类(Ia)抗原的表达增加有关。与体外LC成熟研究类似,此类变化可能受粒细胞/巨噬细胞集落刺激因子(GM-CSF)和白介素-1(IL-1)的影响,这两者都是表皮细胞的产物。问题仍然是引发LC迁移的刺激的性质。在本研究中,我们已经在小鼠中检查了皮内注射另一种表皮细胞因子肿瘤坏死因子-α(TNF-α)对淋巴结中DC积累的影响。发现鼠重组TNF-α引起引流节点内DC数量的浓度和时间依赖性增加。在相同暴露条件下,鼠重组GM-CSF无效。小鼠TNF-α的热处理导致对DC积累和通过体外生物测定法测量的细胞毒性活性具有同等的抑制作用。有趣的观察是,等浓度的同等比活的人TNF-α不能影响淋巴结DC的频率。这些数据表明,TNF-α诱导DC积累在引流淋巴结中,我们建议这种细胞因子可能为皮肤免疫反应中LC迁移提供一种刺激。

著录项

  • 期刊名称 Immunology
  • 作者

    M Cumberbatch; I Kimber;

  • 作者单位
  • 年(卷),期 1992(75),2
  • 年度 1992
  • 页码 257–263
  • 总页数 7
  • 原文格式 PDF
  • 正文语种
  • 中图分类 免疫学;
  • 关键词

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