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首页> 外文期刊>American Journal of Physiology >Increased placental fatty acid transporter 6 and binding protein 3 expression and fetal liver lipid accumulation in a mouse model of obesity in pregnancy
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Increased placental fatty acid transporter 6 and binding protein 3 expression and fetal liver lipid accumulation in a mouse model of obesity in pregnancy

机译:增加胎盘脂肪酸转运蛋白6和结合蛋白3表达和胎儿肝脂肪积累在肥胖的肥胖小鼠模型中

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Obesity in pregnancy is associated with increased fetal growth and adiposity, which, in part, is determined by transplacental nutrient supply, Trophoblast uptake and intracellular trafficking of lipids are dependent on placental fatty acid transport proteins (FATP), translocase (FAT/CD36), and fatty acid binding proteins (FABP). We hypothesized that maternal obesity in mice leads to increased placental expression of FAT/ CD36, FATPs, and FABPs, and lipid accumulation in the fetal liver. C57/BL6J female mice were fed either a control (C; n = 10) or an obesogenic (OB; n = 10) high-fat, high-sugar diet before mating and throughout pregnancy. At E18.5, placentas and fetal livers were collected. Trophoblast plasma membranes (TPM) were isolated from placental homogenates. Expression of FAT/CD36 and FATP (TPM) and FABP (homogenates) was determined by immunoblotting. Gene expression was assessed by RT-quantitative PCR. Sections of fetal livers were stained for Oil Red O, and lipid droplets were quantified. TPM protein expression of FAT/CD36, FATP 2, and FATP 4 was comparable between C and OB groups. Conversely, TPM FATP 6 expression was increased by 35% in OB compared with C placentas without changes in mRNA expression. FABPs 1, 3-5 and PPARgamma were expressed in homogenates, and FABP 3 expression increased 27% in OB compared with C placentas; however, no changes were observed in mRNA expression. Lipid droplet accumulation was 10-fold higher in the livers of fetuses from OB compared with C group. We propose that increased lipid transport capacity in obese mice promotes transplacental fatty acid transport and contributes to excess lipid accumulation in the fetal liver.
机译:怀孕的肥胖与增加的胎儿生长和肥胖有关,部分是通过转血管营养供应,滋养板吸收和细胞内运输脂质依赖于胎盘脂肪酸输送蛋白(FATP),转译(脂肪/ CD36),和脂肪酸结合蛋白(Fabp)。我们假设小鼠的母体肥胖导致胎儿肝脏脂肪/ CD36,FATP和FABP的胎盘表达增加,以及胎儿肝脏的脂质积累。 C57 / BL6J雌性小鼠被喂食(C; n = 10)或在交配和整个怀孕之前的高脂,高糖饮食。在E18.5,收集胎盘和胎儿肝脏。从胎盘匀浆中分离滋养细胞血浆膜(TPM)。通过免疫印迹测定脂肪/ CD36和FATP(TPM)和FABP(匀浆)的表达。通过RT-定量PCR评估基因表达。诱导胎儿肝脏的剖面为油红色o,量化脂液滴。脂肪/ CD36,FATP 2和FATP 4的TPM蛋白表达在C和OB组之间是可比的。相反,与C胎盘相比,TPM FATP 6表达在没有变化的mRNA表达的情况下增加了35%。在匀浆中表达Fabps 1,3-5和Pparγ,与C胎盘相比,FABP 3表达增加了27%;但是,在mRNA表达中没有观察到变化。与C组相比,脂肪液滴积聚在胎儿的肝脏中高10倍。我们提出肥胖小鼠中的脂质传输能力增加促进转脑脂肪酸输送,并有助于胎儿肝脏的过度脂质积累。

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