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首页> 外文期刊>Molecular Immunology >CD25 signaling regulates the function and stability of peripheral Foxp3+regulatory T cells derived from the spleen and lymph nodes of mice
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CD25 signaling regulates the function and stability of peripheral Foxp3+regulatory T cells derived from the spleen and lymph nodes of mice

机译:CD25信号传导调节小鼠脾脏和淋巴结来源的外周Foxp3 +调节性T细胞的功能和稳定性

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Regulatory T cells (Tregs) play a critical role in sustaining immune tolerance and maintaining immune balance to alloantigen after transplatation. However, the functions of peripheral Tregs in different organs have not been fully characterized. Here, we showed that spleen-derived Tregs exhibited higher expression of Foxp3, greater suppressive capacity, and lower levels of IL-17A secretion than lymph node-derived Tregs in vitro in the presence or absence of inflammatory cytokines, such as IL-6. We found a higher percentage of CD25bright Tregs among spleen-derived Tregs than among lymph node -derived Tregs. Additionally, in vivo experiments demonstrated that adoptive transfer of spleen -derived Tregs, but not lymph node-derived Tregs, alleviated ischemia-reperfusion injury. These results reveal novel functions of Tregs derived from peripheral organs. In particular, spleen -derived Tregs, primarily consisting of CD25bright cells, may provide a more significant contribution to the suppression of immune-mediated autoimmune and inflammatory disease. (C) 2016 Elsevier Ltd. All rights reserved.
机译:调节性T细胞(Tregs)在维持免疫耐受和维持转座后同种抗原的免疫平衡方面起着关键作用。然而,尚未充分表征不同器官中外周Treg的功能。在这里,我们显示,在存在或不存在炎性细胞因子(例如IL-6)的情况下,脾脏衍生的Tregs在体外表现出比淋巴结衍生的Tregs高的Foxp3表达,更大的抑制能力和更低的IL-17A分泌水平。我们发现脾源性Treg中CD25亮Treg的百分比高于淋巴结来源Treg。另外,体内实验表明,脾脏来源的Tregs的过继转移,而非淋巴结来源的Tregs的过继转移,减轻了缺血再灌注损伤。这些结果揭示了衍生自外周器官的Treg的新功能。特别地,主要由CD25亮细胞组成的源自脾的Treg可对抑制免疫介导的自身免疫和炎性疾病提供更重要的贡献。 (C)2016 Elsevier Ltd.保留所有权利。

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