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Pluronic Nanoparticles do not Modulate Immune Responses Mounted by Macrophages

机译:Pluronic纳米粒子不会调节巨噬细胞安装的免疫反应。

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Nanomatenals have been developed for the target delivery of medicine because they shbwfhe characteristics of selective emission or controlled release Although accumulated data suggest the efficacy of these materials for the target delivery, it still remams to be determined whether they modulate immune responses to paihogens or foreign materials In this study, we examined whether Pluromc nanoparticles (NPs),a type of nanomaterial, alter immune responses mediated by macrophages When RAW 264 7 cells (RAW cells) were treated with Pluronic NPs in the presence or absence of lipopolysaccharides (LPS), they produced normal levels of nitrie oxide(NO).Further-more, the treatment with Pluronic nanomatenals did not induce cytotoxicity with or without LPS. Further, LPS-Stim-ulated RAW cells expressed comparable levels of proinflammatory cytokine genes, such as interleukin (IL)-1β, IL-6 and tumor necrosis factor (TNF)-a, with or without treatment by Pluromc NPs These data suggest that Pluromc NPs do not modulate immune responses mediated by macrophages
机译:由于纳米材料具有选择性发射或控释的特性,因此已开发出用于药物靶标的纳米材料。尽管积累的数据表明这些材料对靶标材料的功效,但仍需要确定它们是否调节对致癌物或异物的免疫反应。在这项研究中,我们检查了Pluromc纳米颗粒(NPs)是一种纳米材料,是否改变了巨噬细胞介导的免疫反应。在存在或不存在脂多糖(LPS)的情况下,使用Pluronic NPs处理RAW 264 7细胞(RAW细胞)时,它们产生正常水平的一氧化二氮(NO)。此外,使用或不使用LPS的Pluronic纳米材料治疗均不会诱导细胞毒性。此外,LPS刺激的RAW细胞在经过或未经过Pluromc NP处理的情况下,均表达了相当水平的促炎细胞因子基因,例如白介素(IL)-1β,IL-6和肿瘤坏死因子(TNF)-a。这些数据表明Pluromc NP不调节巨噬细胞介导的免疫反应

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