PHF-2在氧化型低密度脂蛋白诱导THP-1源性
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国家自然科学基金(81100213);湖南省研究生科研创新项目(2012SCX13);国家级大学生创新创业训练计划(201210555018)


The Role of Plant Homeodomain Finger-2 in Oxidized Low Density Lipoprotein-induced Activation of Nuclear Factor-kappa B in THP-1 Macrophages
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    摘要:

    目的 观察氧化型低密度脂蛋白对THP-1巨噬细胞植物同源结构域指蛋白2(PHF-2)表达的影响,探讨表观遗传调节在氧化型低密度脂蛋白诱导巨噬细胞炎症反应中的作用。方法 用不同浓度(0、50、100、150 mg/L)氧化型低密度脂蛋白处理THP-1巨噬细胞4 h,采用酶联免疫吸附法检测肿瘤坏死因子α和巨噬细胞炎性蛋白1β的表达;采用实时荧光定量聚合酶链反应和Western blot分别检测PHF-2 mRNA和蛋白质的表达;采用免疫共沉淀法检测PHF-2和p65核因子κB的结合。结果 100~150 mg/L氧化型低密度脂蛋白处理THP-1巨噬细胞4 h后,肿瘤坏死因子α和巨噬细胞炎性蛋白1β的表达明显上调;氧化型低密度脂蛋白呈浓度依赖性上调THP-1巨噬细胞PHF-2 mRNA和蛋白质的表达,并促进PHF-2和p65核因子κB的结合。结论 PHF-2参与氧化型低密度脂蛋白诱导THP-1巨噬细胞核因子κB激活和炎症因子表达。

    Abstract:

    Aim To investigate the effect of oxidized low density lipoprotein (ox-LDL) on the expression of plant homeodomain finger-2 (PHF-2) and explore the potential effect of epigenetic regulation on ox-LDL-induced inflammatory response in macrophages. Methods THP-1 macrophages were exposed to ox-LDL with different levels (0, 50, 100, 150 mg/L) for 4 h. Enzyme linked immunosorbent assay was used to determine levels of tumor necrosis factor-α (TNF-α) and macrophage inflammatory protein-1β (MIP-1β). Real-time quantitative polymerase chain reaction (Real-time PCR) and Western blot were used to determine mRNA and protein levels of PHF-2. Coimmunoprecipitation was used to determine the interaction of PHF-2 and p65 nuclear factor-kappa B (p65 NF-κB). Results ox-LDL from 100 mg/L to 150 mg/L increased the levels of TNF-α and MIP-1β. PHF-2 mRNA and protein were induced by ox-LDL in a concentration-dependent manner in THP-1 macrophages. Ox-LDL promoted the interaction of PHF-2 and p65 NF-κB. Conclusion PHF-2 may play a crucial role in the NF-κB activation and proinflammatroy cytokines expression in THP-1 macrophages.

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涂光辉,李金凤,谢 笛,桂庆军,唐朝克,尹 凯. PHF-2在氧化型低密度脂蛋白诱导THP-1源性[J].中国动脉硬化杂志,2013,21(09):780~784.

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  • 收稿日期:2013-05-13
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