首页> 外文期刊>亚太热带医药杂志(英文版) >Higher production of tumor necrosis factor alpha in hemozoin-fed human adherent monocytes is dependent on lipidic component of malarial pigment:new evidences on cytokine regulation inPlasmodium falciparummalaria
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Higher production of tumor necrosis factor alpha in hemozoin-fed human adherent monocytes is dependent on lipidic component of malarial pigment:new evidences on cytokine regulation inPlasmodium falciparummalaria

机译:靠血红素喂养的人类贴壁单核细胞中肿瘤坏死因子α的更高产量取决于疟疾色素的脂质成分:恶性疟原虫细胞因子调控的新证据

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摘要

Objective:To investigate whether the increase of tumor necrosis factor alpha is dependent on lipidic component of malarial pigment.Methods: Adherent human monocytes were fed for 3 hours with different meals (native hemozoin; lipid free hemozoin; and control latex particles), then tumor necrosis factor alpha was monitored in cell supernatants up to 48 hours through western blotting or specific enzyme-linked immunoadsorbent assay. In selected experiments, unfed monocytes were treated with different doses of 15(S,R)-hydroxy-6,8,11,13-eicosatetraenoic acid or 4-hydroxynonenal instead of phagocytosis.Results: Hemozoin-fed monocytes produced higher levels of tumor necrosis factor alpha than unstimulated and latex-fed cells, while lipid-free hemozoin did not reproduce these results. Additionally, hemozoin effects were mimicked dose-dependently by 15(S,R)-hydroxy-6,8,11,13-eicosatetraenoic acid, but not by 4-hydroxynonenal.Conclusions: Present data suggest an essential role for lipids in hemozoin-dependent enhanced release of tumor necrosis factor alpha from monocytes, and 15(S,R)-hydroxy-6,8,11,13-eicosatetraenoic acid could be one possible specific mediator.
机译:目的:研究肿瘤坏死因子α的增加是否与疟疾色素的脂质成分有关。方法:将人单核细胞粘附3小时,分别饲喂天然血红蛋白,无脂质血红蛋白和对照乳胶颗粒,然后进食肿瘤通过蛋白质印迹或特异性酶联免疫吸附测定法,在细胞上清液中监测坏死因子α长达48小时。在选定的实验中,未喂养的单核细胞用不同剂量的15(S,R)-羟基-6,8,11,13-二十碳四烯酸或4-羟基壬烯醛代替吞噬作用进行治疗。结果:血红素喂养的单核细胞产生更高水平的肿瘤坏死因子α比未刺激和乳胶喂养的细胞要好,而无脂质的zozoin没有重现这些结果。此外,用15(S,R)-羟基-6,8,11,13-二十碳四烯酸来剂量依赖性地模拟血红蛋白的作用,但不能用4-羟基壬烯醛来模拟血红蛋白的作用。结论:目前的数据表明脂质在血红蛋白-中的重要作用依赖的单核细胞中肿瘤坏死因子α的增强释放,以及15(S,R)-羟基-6,8,11,13-二十碳四烯酸可能是一种可能的特异性介体。

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    《亚太热带医药杂志(英文版)》 |2010年第002期|85-89|共5页
  • 作者单位

    Department of Genetics, Biology and Biochemistry, University of Torino Medical School, Torino, Italy;

    Department of Genetics, Biology and Biochemistry, University of Torino Medical School, Torino, Italy;

    Department of Genetics, Biology and Biochemistry, University of Torino Medical School, Torino, Italy;

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