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首页> 外文期刊>American Journal of Translational Research >mKLRL1 regulates the maturation of dendritic cells and plays important roles in immune tolerance
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mKLRL1 regulates the maturation of dendritic cells and plays important roles in immune tolerance

机译:mKLRL1调节树突状细胞的成熟并在免疫耐受中起重要作用

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KLRL1 is a member of C-type lectin-like receptors (CLEC) and preferentially expressed on the surface of immune cells. We have previously illustrated its inhibitory role in Natural killer (NK) cells. Though cloned from dendritic cells (DCs), its role in DCs has not been fully identified. Here, we found that mKLRL1 markedly decreased during DC maturation; mKLRL1-modifed DCs showed enhanced phagocytic capability and reduced ability to induce T cell proliferation, which mimics immature DCs. Further investigation revealed that IL-10 was indispensable for mKLRL1 to suppress DC maturation. And p38 activation was responsible for preferential IL-10 production. Pretreatment with mKLRL1-modified DCs protected mice from subsequently EAE induction, indicating a role in immune tolerance. Taken together, our results have revealed an inhibitory role of KLRL1 in mouse DCs.
机译:KLRL1是C型凝集素样受体(CLEC)的成员,并优先在免疫细胞表面表达。我们先前已经说明了其在自然杀伤(NK)细胞中的抑制作用。尽管从树突状细胞(DC)克隆,但其在DC中的作用尚未完全确定。在这里,我们发现mKLRL1在DC成熟过程中明显降低; mKLRL1修饰的DC表现出增强的吞噬能力,​​并降低了诱导T细胞增殖的能力,从而模仿了未成熟的DC。进一步的研究表明,IL-10对于抑制mKLRL1抑制DC成熟是必不可少的。 p38激活负责IL-10的优先生产。用mKLRL1修饰的DC进行预处理可保护小鼠免于随后的EAE诱导,表明其在免疫耐受中起作用。两者合计,我们的结果表明KLRL1在小鼠DC中的抑制作用。

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