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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:妊娠肥胖小鼠模型中胎盘脂肪酸转运蛋白6和结合蛋白3的表达增加以及胎儿肝脂质蓄积

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摘要

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 PPARγ 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:怀孕期间的肥胖与胎儿生长和肥胖的增加有关,这部分取决于胎盘的营养供应。滋养细胞的摄取和脂质的细胞内运输取决于胎盘脂肪酸转运蛋白(FATP),转位酶(FAT / CD36)和脂肪酸结合蛋白(FABP)。我们假设母体肥胖会导致胎盘中FAT / CD36,FATP和FABP的胎盘表达增加,以及胎儿肝脏中的脂质蓄积。 C57 / BL6J雌性小鼠在交配前和整个怀孕期间均饲喂了对照(C; n = 10)或致肥胖(OB; n = 10)高脂,高糖饮食。在E18.5,收集胎盘和胎儿肝脏。从胎盘匀浆中分离出滋养层质膜(TPM)。 FAT / CD36和FATP(TPM)和FABP(均质)的表达通过免疫印迹法确定。通过RT定量PCR评估基因表达。对胎儿肝脏切片进行油红O染色,并对脂质滴定量。 FAT / CD36,FATP 2和FATP 4的TPM蛋白表达在C组和OB组之间相当。相反,与C胎盘相比,OB中TPM FATP 6表达增加了35%,而mRNA表达没有变化。 FABP 1、3-5和PPARγ在匀浆中表达,与C胎盘相比,OB中FABP 3的表达增加27%。然而,在mRNA表达中未观察到变化。与C组相比,OB组胎儿肝脏中的脂质液滴积累高10倍。我们建议增加肥胖小鼠脂质运输能力促进胎盘脂肪酸运输,并有助于胎儿肝脏中过多的脂质积累。

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