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Propofol Suppresses Proinflammatory Cytokine Production by Increasing ABCA1 Expression via Mediation by the Long Noncoding RNA LOC286367

机译:通过通过长的非数量RNA LOC286367通过调解增加ABCA1表达,PROPOFOL抑制促炎细胞因子产生

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摘要

We previously reported that propofol upregulated the expression of ATP-binding cassette transporter subfamily A member 1 (ABCA1) via peroxisome proliferator-activated receptor gamma/liver X receptor in macrophage-derived foam cells. Here, we provide evidence that in addition to inducing ABCA1 expression, propofol represses proinflammatory cytokine production by increasing ABCA1 expression in a LOC286367-dependent manner. Western blot analysis showed that ABCA1 expression was elevated in macrophages by propofol treatment and this effect was markedly reduced by LOC286367 overexpression. Moreover, propofol treatment downregulated the production of the proinflammatory cytokines interleukin-6, tumor necrosis factor, and interferon gamma in lipopolysaccharide-stimulated macrophages by enhancing ABCA1 expression. Notably, propofol achieved this effect in a LOC286367-dependent manner. To the best of our knowledge, this is the first report of the mechanism in which propofol represses proinflammatory cytokine production mediated by ABCA1.
机译:我们之前报道了ProPofol在巨噬细胞衍生的泡沫细胞中通过过氧缺体增殖物激活的受体γ/肝X受体将ATP结合盒式磁带转运蛋白A(ABCA1)的表达上调。在这里,我们提供了证据,除了诱导ABCA1表达外,异丙酚还通过增加依赖于LOM286367的依赖性的ABCA1表达来抑制促炎细胞因子产生。 Western印迹分析表明,ABCA1表达通过异丙酚处理在巨噬细胞中升高,并且通过LOM286367过表达显着降低了这种效果。此外,通过增强ABCA1表达,Proofol治疗下调了脂多糖刺激的巨噬细胞的促炎细胞因子白细胞介素-6,肿瘤坏死因子和干扰素γ。值得注意的是,异丙酚以依赖于LOC286367依赖性的方式实现了这种效果。据我们所知,这是第一个机制的第一个报告,其中丙糊酚抑制由ABCA1介导的促炎细胞因子生产。

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