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首页> 外文期刊>Lipids in Health Disease >Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9
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Decreased APOE-containing HDL subfractions and cholesterol efflux capacity of serum in mice lacking Pcsk9

机译:缺乏Pcsk9的小鼠中含APOE的HDL亚组分和血清胆固醇外排能力降低

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Background Studies in animals showed that PCSK9 is involved in HDL metabolism. We investigated the molecular mechanism by which PCSK9 regulates HDL cholesterol concentration and also whether Pcsk9 inactivation might affect cholesterol efflux capacity of serum and atherosclerotic fatty streak volume. Methods Mass spectrometry and western blot were used to analyze the level of apolipoprotein E (APOE) and A1 (APOA1). A mouse model overexpressing human LDLR was used to test the effect of high levels of liver LDLR on the concentration of HDL cholesterol and APOE-containing HDL subfractions. Pcsk9 knockout males lacking LDLR and APOE were used to test whether LDLR and APOE are necessary for PCSK9-mediated HDL cholesterol regulation. We also investigated the effects of Pcsk9 inactivation on cholesterol efflux capacity of serum using THP-1 and J774.A1 macrophage foam cells and atherosclerotic fatty streak volume in the aortic sinus of Pcsk9 knockout males fed an atherogenic diet. Results APOE and APOA1 were reduced in the same HDL subfractions of Pcsk9 knockout and human LDLR transgenic male mice. In Pcsk9/Ldlr double-knockout mice, HDL cholesterol concentration was lower than in Ldlr knockout mice and higher than in wild-type controls. In Pcsk9/Apoe double-knockout mice, HDL cholesterol concentration was similar to that of Apoe knockout males. In Pcsk9 knockout males, THP-1 macrophage cholesterol efflux capacity of serum was reduced and the fatty streak lesion volume was similar to wild-type controls. Conclusions In mice, LDLR and APOE are important factors for PCSK9-mediated HDL regulation. Our data suggest that, although LDLR plays a major role in PCSK9-mediated regulation of HDL cholesterol concentration, it is not the only mechanism and that, regardless of mechanism, APOE is essential. Pcsk9 inactivation decreases the HDL cholesterol concentration and cholesterol efflux capacity in serum, but does not increase atherosclerotic fatty streak volume.
机译:动物背景研究表明PCSK9参与HDL代谢。我们研究了PCSK9调节HDL胆固醇浓度的分子机制,以及Pcsk9失活是否可能影响血清的胆固醇外流能力和动脉粥样硬化性脂肪的体积。方法采用质谱和蛋白质印迹法分析载脂蛋白E(APOE)和A1(APOA1)的水平。使用过表达人LDLR的小鼠模型来测试高水平肝脏LDLR对HDL胆固醇和含APOE的HDL组分浓度的影响。缺乏LDLR和APOE的Pcsk9基因敲除雄性用于测试LDLR和APOE对于PCSK9介导的HDL胆固醇调节是否必要。我们还研究了THC-1和J774对Pcsk9失活对血清胆固醇外排能力的影响。饲喂有动脉粥样化饮食的Pcsk9剔除雄性主动脉窦中,A1巨噬细胞泡沫细胞和主动脉窦有动脉粥样硬化脂肪条纹。结果在Pcsk9基因敲除和人LDLR转基因雄性小鼠的相同HDL亚组中,APOE和APOA1降低。在Pcsk9 / Ldlr双敲除小鼠中,HDL胆固醇浓度低于Ldlr敲除小鼠,但高于野生型对照。在Pcsk9 / Apoe双敲除小鼠中,HDL胆固醇浓度与Apoe敲除雄性相似。在Pcsk9基因敲除的男性中,血清THP-1巨噬细胞胆固醇外排能力降低,并且脂肪条纹病变体积与野生型对照相似。结论在小鼠中,LDLR和APOE是PCSK9介导的HDL调节的重要因素。我们的数据表明,尽管LDLR在PCSK9介导的HDL胆固醇浓度调节中起主要作用,但它不是唯一的机制,且无论机制如何,APOE都是必不可少的。 Pcsk9失活会降低血清中HDL胆固醇浓度和胆固醇外排能力,但不会增加动脉粥样硬化性脂肪的体积。

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