Suppr超能文献

母体高脂喂养通过降低小鼠体内SIRT1表达来增加胎盘脂蛋白脂肪酶活性。

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

作者信息

Qiao Liping, Guo Zhuyu, Bosco Chris, Guidotti Stefano, Wang Yunfeng, Wang Mingyong, Parast Mana, Schaack Jerome, Hay William W, Moore Thomas R, Shao Jianhua

机构信息

Department of Pediatrics, University of California San Diego, La Jolla, CA.

Department of Pediatrics, China-Japan Friendship Hospital, Beijing, China.

出版信息

Diabetes. 2015 Sep;64(9):3111-20. doi: 10.2337/db14-1627. Epub 2015 May 6.

Abstract

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.

摘要

本研究调查了母体营养过剩和肥胖如何调节胎盘脂质转运相关蛋白的表达与激活。为建立母体营养过剩和肥胖模型,初产C57BL/6小鼠在整个妊娠期均喂食高脂(HF)饮食。来自喂食HF饮食母鼠的胎儿血清游离脂肪酸水平和体脂显著增加。尽管胎盘重量无显著差异,但喂食HF饮食母鼠的胎盘脂蛋白脂肪酶(LPL)蛋白水平和活性显著升高。在喂食HF饮食母鼠的胎盘中还发现甘油三酯含量增加,以及CD36、极低密度脂蛋白受体(VLDLr)、脂肪酸结合蛋白3(FABP3)、胎盘脂肪酸结合蛋白(FABPpm)和甘油磷酸酰基转移酶2(GPAT2)及-3的mRNA水平升高。虽然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蛋白水平在HF组胎盘中均显著增加,但只有PPARγ对培养的JEG-3人滋养层细胞中的LPL表达具有刺激作用。母体喂食HF显著降低了胎盘中沉默信息调节因子1(SIRT1)的表达。通过使用SIRT1激活剂和抑制剂以及培养的滋养层细胞,证实了SIRT1对LPL表达具有抑制作用。我们还发现SIRT1抑制滋养层细胞中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降低SIRT1对PPARγ的抑制作用诱导滋养层细胞中LPL的表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e695/4542442/a42d3cb18826/db141627f1-1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验