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Maternal High-Fat Feeding Increases Placental Lipoprotein Lipase Activity by Reducing SIRT1 Expression in Mice

机译:孕妇高脂喂养通过降低小鼠SIRT1的表达来增加胎盘脂蛋白脂肪酶的活性

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摘要

This study investigated how maternal overnutrition and obesity regulate expression and activation of proteins that facilitate lipid transport in the placenta. To create a maternal overnutrition and obesity model, primiparous C57BL/6 mice were fed a high-fat (HF) diet throughout gestation. Fetuses from HF-fed dams had significantly increased serum levels of free fatty acid and body fat. Despite no significant difference in placental weight, lipoprotein lipase (LPL) protein levels and activity were remarkably elevated in placentas from HF-fed dams. Increased triglyceride content and mRNA levels of CD36, VLDLr, FABP3, FABPpm, and GPAT2 and -3 were also found in placentas from HF-fed dams. Although both peroxisome proliferator–activated receptor-γ (PPARγ) and CCAAT/enhancer binding protein-α protein levels were significantly increased in placentas of the HF group, only PPARγ exhibited a stimulative effect on LPL expression in cultured JEG-3 human trophoblasts. Maternal HF feeding remarkably decreased SIRT1 expression in placentas. Through use of an SIRT1 activator and inhibitor and cultured trophoblasts, an inhibitory effect of SIRT1 on LPL expression was demonstrated. We also found that SIRT1 suppresses PPARγ expression in trophoblasts. Most importantly, inhibition of PPARγ abolished the SIRT1-mediated regulatory effect on LPL expression. Together, these results indicate that maternal overnutrition induces LPL expression in trophoblasts by reducing the inhibitory effect of SIRT1 on PPARγ.
机译:这项研究调查了母亲过度营养和肥胖如何调节蛋白质的表达和激活,从而促进胎盘中脂质的运输。为了创建孕产妇营养过剩和肥胖症模型,在整个妊娠过程中,给初生C57BL / 6小鼠喂食高脂(HF)饮食。用HF喂养的大坝中的胎儿血清中的游离脂肪酸和人体脂肪水平显着增加。尽管胎盘重量没有显着差异,但HF喂养大坝的胎盘中脂蛋白脂肪酶(LPL)蛋白水平和活性显着提高。在HF喂养的大坝的胎盘中也发现了CD36,VLDLr,FABP3,FABPpm,GPAT2和-3的甘油三酸酯含量和mRNA水平的增加。尽管HF组胎盘中的过氧化物酶体增殖物激活受体-γ(PPARγ)和CCAAT /增强子结合蛋白-α蛋白水平均显着增加,但只有PPARγ对培养的JEG-3人滋养细胞中的LPL表达具有刺激作用。母体HF喂养显着降低胎盘SIRT1表达。通过使用SIRT1激活剂和抑制剂以及培养的滋养细胞,证明了SIRT1对LPL表达的抑制作用。我们还发现SIRT1抑制滋养细胞中PPARγ的表达。最重要的是,抑制PPARγ消除了SIRT1介导的对LPL表达的调节作用。总之,这些结果表明,母体营养过剩通过减少SIRT1对PPARγ的抑制作用而在滋养细胞中诱导LPL表达。

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