首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid
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Small intestine lamina propria dendritic cells promote de novo generation of Foxp3 T reg cells via retinoic acid

机译:小肠固有层树突状细胞通过视黄酸促进Foxp3 T reg细胞的新生

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摘要

To maintain immune homeostasis, the intestinal immune system has evolved redundant regulatory strategies. In this regard, the gut is home to a large number of regulatory T (T reg) cells, including the Foxp3+ T reg cell. Therefore, we hypothesized that the gut environment preferentially supports extrathymic T reg cell development. We show that peripheral conversion of CD4+ T cells to T reg cells occurs primarily in gut-associated lymphoid tissue (GALT) after oral exposure to antigen and in a lymphopenic environment. Dendritic cells (DCs) purified from the lamina propria (Lp; LpDCs) of the small intestine were found to promote a high level of T reg cell conversion relative to lymphoid organ–derived DCs. This enhanced conversion by LpDCs was dependent on TGF-β and retinoic acid (RA), which is a vitamin A metabolite highly expressed in GALT. Together, these data demonstrate that the intestinal immune system has evolved a self-contained strategy to promote T reg cell neoconversion.
机译:为了维持免疫稳态,肠道免疫系统已经进化出多余的调节策略。在这方面,肠道是大量调节性T(T reg)细胞的所在地,包括Foxp3 + T reg细胞。因此,我们假设肠道环境优先支持胸腺外T reg细胞的发育。我们表明,CD4 + T细胞向T reg细胞的外周转化主要发生在口服抗原后和在淋巴细胞减少的环境中,与肠道相关的淋巴样组织(GALT)中。发现从小肠固有层(Lp; LpDCs)纯化的树突状细胞(DC)相对于淋巴器官来源的DC促进高水平的T reg细胞转化。 LpDC的这种增强的转化取决于TGF-β和视黄酸(RA),后者是在GALT中高度表达的维生素A代谢产物。总之,这些数据表明肠道免疫系统已发展出一种自成一体的策略来促进T reg细胞新转化。

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