Lie Shervi, Morrison Janna L, Williams-Wyss Olivia, Suter Catherine M, Humphreys David T, Ozanne Susan E, Zhang Song, MacLaughlin Severence M, Kleemann David O, Walker Simon K, Roberts Claire T, McMillen I Caroline
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, Australia;
Sansom Institute for Health Research, School of Pharmacy and Medical Sciences, University of South Australia, Adelaide, Australia; Discipline of Physiology, School of Medical Sciences, University of Adelaide, Adelaide, Australia;
Am J Physiol Endocrinol Metab. 2016 Jan 15;310(2):E148-59. doi: 10.1152/ajpendo.00600.2014. Epub 2015 Oct 20.
We have investigated the effects of embryo number and maternal undernutrition imposed either around the time of conception or before implantation on hepatic lipid metabolism in the sheep fetus. We have demonstrated that periconceptional undernutrition and preimplantation undernutrition each resulted in decreased hepatic fatty acid β-oxidation regulators, PGC-1α (P < 0.05), PDK2 (P < 0.01), and PDK4 (P < 0.01) mRNA expression in singleton and twin fetuses at 135-138 days gestation. In singletons, there was also lower hepatic PDK4 (P < 0.01), CPT-1 (P < 0.01), and PKCζ (P < 0.01) protein abundance in the PCUN and PIUN groups and a lower protein abundance of PDPK-1 (P < 0.05) in the PCUN group. Interestingly, in twins, the hepatic protein abundance of p-AMPK (Ser(485)) (P < 0.01), p-PDPK-1 (Ser(41)) (P < 0.05), and PKCζ (P < 0.05) was higher in the PCUN and PIUN groups, and hepatic PDK4 (P < 0.001) and CPT-1 (P < 0.05) protein abundance was also higher in the PIUN twin fetus. We also found that the expression of a number of microRNAs was altered in response to PCUN or PIUN and that there is evidence that these changes may underlie the changes in the protein abundance of key regulators of hepatic fatty acid β-oxidation in the PCUN and PIUN groups. Therefore, embryo number and the timing of maternal undernutrition in early pregnancy have a differential impact on hepatic microRNA expression and on the factors that regulate hepatic fatty acid oxidation and lipid synthesis.
我们研究了受孕前后或着床前施加的胚胎数量和母体营养不足对绵羊胎儿肝脏脂质代谢的影响。我们已经证明,受孕前后营养不足和着床前营养不足均导致妊娠135 - 138天时单胎和双胎胎儿肝脏脂肪酸β -氧化调节因子PGC - 1α(P < 0.05)、PDK2(P < 0.01)和PDK4(P < 0.01)的mRNA表达降低。在单胎中,PCUN和PIUN组肝脏中PDK4(P < 0.01)、CPT - 1(P < 0.01)和PKCζ(P < 0.01)的蛋白丰度也较低,PCUN组中PDPK - 1的蛋白丰度较低(P < 0.05)。有趣的是,在双胎中,PCUN和PIUN组肝脏中p - AMPK(Ser(485))(P < 0.01)、p - PDPK - 1(Ser(41))(P < 0.05)和PKCζ(P < 0.05)的蛋白丰度较高,PIUN双胎胎儿肝脏中PDK4(P < 0.001)和CPT - 1(P < 0.05)的蛋白丰度也较高。我们还发现,许多微小RNA的表达因PCUN或PIUN而改变,并且有证据表明这些变化可能是PCUN和PIUN组中肝脏脂肪酸β -氧化关键调节因子蛋白丰度变化的基础。因此,胚胎数量和孕早期母体营养不足的时间对肝脏微小RNA表达以及调节肝脏脂肪酸氧化和脂质合成的因素有不同影响。