首页> 美国卫生研究院文献>Infection and Immunity >Fatty Acids Isolated from Toxoplasma gondii Reduce Glycosylphosphatidylinositol-Induced Tumor Necrosis Factor Alpha Production through Inhibition of the NF-κB Signaling Pathway
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Fatty Acids Isolated from Toxoplasma gondii Reduce Glycosylphosphatidylinositol-Induced Tumor Necrosis Factor Alpha Production through Inhibition of the NF-κB Signaling Pathway

机译:从弓形虫中分离出的脂肪酸通过抑制NF-κB信号通路降低糖基磷脂酰肌醇的糖基化诱导的肿瘤坏死因子的产生

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摘要

Glycosylphosphatidylinositols (GPIs) are involved in the pathogenicity of protozoan parasites and are known to induce inflammatory cytokines. However, we have previously shown that the family of six GPIs of Toxoplasma gondii extracted together from tachyzoites could not induce tumor necrosis factor alpha (TNF-α) secretion by macrophages, whereas GPIs individually separated from this extract by thin-layer chromatography (TLC) were able to stimulate the cells. In the present study we show that the TLC step makes it possible to eliminate inhibitors extracted together with the T. gondii GPIs. Among the non-GPI molecules we have isolated fatty acids able to inhibit the secretion of TNF-α induced by the T. gondii GPIs. Myristic and palmitic acids reduce the production of TNF-α through the inhibition of tyrosine phosphorylation of cytoplasmic proteins and the inhibition of NF-κB activation in a peroxisome proliferator-activated receptor-independent pathway and after a rapid entry into the cytoplasm of macrophages. GPIs are considered toxins inducing irreversible damage in the host, and fatty acids produced in parallel by the parasite could reduce the immune response, thus favoring the persistence of parasite infection.
机译:糖基磷脂酰肌醇(GPI)参与原生动物寄生虫的致病性,并已知可诱导炎症性细胞因子。但是,我们以前已经表明,从速殖子一起提取的弓形虫的六个GPI家族不能诱导巨噬细胞分泌肿瘤坏死因子α(TNF-α),而GPI则通过薄层色谱法(TLC)单独分离出来能够刺激细胞。在本研究中,我们表明TLC步骤可以消除与弓形虫GPI一起提取的抑制剂。在非GPI分子中,我们分离出能够抑制弓形虫GPI诱导的TNF-α分泌的脂肪酸。肉豆蔻酸和棕榈酸通过抑制细胞质蛋白的酪氨酸磷酸化和抑制过氧化物酶体增殖物激活的受体非依赖性途径以及迅速进入巨噬细胞的细胞质后抑制NF-κB的活化来减少TNF-α的产生。 GPI被认为是在宿主中引起不可逆损害的毒素,寄生虫并行产生的脂肪酸可降低免疫反应,从而有利于寄生虫感染的持续存在。

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