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Cholera toxin induces cAMP-dependent Th17 differentiation by dendritic cells.

机译:霍乱毒素通过树突状细胞诱导cAMP依赖性Th17分化。

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摘要

Cholera toxin (CT), the causative factor responsible for the life-threatening acute diarrhea caused by Vibrio cholerae, is also well known as a potent mucosal vaccine adjuvant. However, little is known about the cellular and molecular mechanisms that mediate the mucosal adjuvant properties of CT. Recent studies have shown that Th17 cells discovered at mucosal sites have important role in generating strong immune responses that can be either protective (e.g. antimicrobial immunity) or destructive (e.g. autoimmune diseases EAE). Here, we showed that CT activates dendritic cells (DC) via cAMP-dependent mechanisms to drive the differentiation of naive T cells into IL-17-producing Th17 cells in vitro and in vivo. Importantly, we identified an alternative pathway for Th17 differentiation that depends on the CT-induced secretion of calcitonin gene-related peptide (CGRP) by DC but is independent of IL-6. CGRP, a neuropeptide, in turn activates cAMP-dependent pathways in T cells that contribute to the generation of Th17 cells. These findings implicate Th17 induction as a contributing factor to the adjuvant effects of CT and identify novel pathways involved in T cell differentiation at mucosal sites.
机译:霍乱毒素(CT),是由霍乱弧菌引起的危及生命的急性腹泻的病因,也是众所周知的强效粘膜疫苗佐剂。但是,关于介导CT的粘膜佐剂特性的细胞和分子机制知之甚少。最近的研究表明,在粘膜部位发现的Th17细胞在产生强大的免疫反应中具有重要作用,这些免疫反应可以是保护性的(例如抗微生物免疫)或破坏性的(例如自身免疫性疾病EAE)。在这里,我们显示CT通过cAMP依赖性机制激活树突状细胞(DC),以在体外和体内驱动幼稚T细胞分化为产生IL-17的Th17细胞。重要的是,我们确定了Th17分化的另一种途径,这取决于CT诱导的DC降钙素基因相关肽(CGRP)的分泌,但独立于IL-6。 CGRP(一种神经肽)反过来激活T细胞中依赖cAMP的途径,从而有助于Th17细胞的生成。这些发现暗示Th17诱导是CT的辅助作用的一个因素,并确定了粘膜部位T细胞分化的新途径。

著录项

  • 作者

    Nguyen, Kim Phung Le.;

  • 作者单位

    University of California, San Diego.;

  • 授予单位 University of California, San Diego.;
  • 学科 Immunology.
  • 学位 M.S.
  • 年度 2009
  • 页码 66 p.
  • 总页数 66
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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