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The Polyunsaturated Fatty Acids Arachidonic Acid and Docosahexaenoic Acid Induce Mouse Dendritic Cells Maturation but Reduce T-Cell Responses In Vitro

机译:多不饱和脂肪酸花生四烯酸和二十二碳六烯酸可诱导小鼠树突状细胞成熟但可降低体外T细胞反应。

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摘要

Long-chain polyunsaturated fatty acids (PUFAs) might regulate T-cell activation and lineage commitment. Here, we measured the effects of omega-3 (n-3), n-6 and n-9 fatty acids on the interaction between dendritic cells (DCs) and naïve T cells. Spleen DCs from BALB/c mice were cultured in vitro with ovalbumin (OVA) with 50 μM fatty acids; α-linolenic acid, arachidonic acid (AA), eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), linoleic acid or oleic acid and thereafter OVA-specific DO11.10 T cells were added to the cultures. Fatty acids were taken up by the DCs, as shown by gas chromatography analysis. After culture with arachidonic acid or DHA CD11c+ CD11b+ and CD11c+ CD11bneg DCs expressed more CD40, CD80, CD83, CD86 and PDL-1, while IAd remained unchanged. However, fewer T cells co-cultured with these DCs proliferated (CellTrace Violetlow) and expressed CD69 or CD25, while more were necrotic (7AAD+). We noted an increased proportion of T cells with a regulatory T cell (Treg) phenotype, i.e., when gating on CD4+ FoxP3+ CTLA-4+, CD4+ FoxP3+ Helios+ or CD4+ FoxP3+ PD-1+, in co-cultures with arachidonic acid- or DHA-primed DCs relative to control cultures. The proportion of putative Tregs was inversely correlated to T-cell proliferation, indicating a suppressive function of these cells. With arachidonic acid DCs produced higher levels of prostaglandin E2 while T cells produced lower amounts of IL-10 and IFNγ. In conclusion arachidonic acid and DHA induced up-regulation of activation markers on DCs. However arachidonic acid- and DHA-primed DCs reduced T-cell proliferation and increased the proportion of T cells expressing FoxP3, indicating that these fatty acids can promote induction of regulatory T cells.
机译:长链多不饱和脂肪酸(PUFA)可能调节T细胞活化和沿袭承诺。在这里,我们测量了omega-3(n-3),n-6和n-9脂肪酸对树突状细胞(DC)与幼稚T细胞之间相互作用的影响。将BALB / c小鼠的脾脏DC与卵清蛋白(OVA)和50μM脂肪酸进行体外培养;将α-亚麻酸,花生四烯酸(AA),二十碳五烯酸(EPA),二十二碳六烯酸(DHA),亚油酸或油酸,然后向培养物中添加OVA特异性DO11.10 T细胞。如气相色谱分析所示,脂肪酸被DC吸收。用花生四烯酸或DHA培养后,CD11b + CD11b + 和CD11c + CD11b neg DC表现出更多的CD40,CD80 ,CD83,CD86和PDL-1,而IA d 保持不变。然而,与这些DC共培养的T细胞增殖较少(CellTrace Violet low )并表达CD69或CD25,而更多的坏死细胞(7AAD + )。我们注意到具有调节性T细胞(Treg)表型的T细胞比例增加,即,在CD4 + FoxP3 + CTLA-4 + ,CD4 + FoxP3 + Helios + 或CD4 + FoxP3 + PD相对于对照培养物,在与花生四烯酸或DHA引发的DC的共培养物中,-1 + 。假定的Tregs的比例与T细胞增殖成反比,表明这些细胞具有抑制功能。用花生四烯酸,DC产生较高水平的前列腺素E2,而T细胞产生较低量的IL-10和IFNγ。总之,花生四烯酸和DHA诱导DC上激活标记的上调。但是,花生四烯酸和DHA引发的DC减少了T细胞增殖,并增加了表达FoxP3的T细胞的比例,表明这些脂肪酸可以促进诱导调节性T细胞。

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