Centre for Trophoblast Research, Department of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3EG, UK.
J Physiol. 2010 Feb 1;588(Pt 3):527-38. doi: 10.1113/jphysiol.2009.181214. Epub 2009 Nov 30.
Undernutrition during pregnancy reduces birth weight and programmes adult phenotype with consequences for life expectancy, but its effects on the phenotype of the placenta, responsible for supplying nutrients for fetal growth, remain largely unknown. Using molecular, morphological and functional analyses, placental phenotype was examined in mice during restriction of dietary intake to 80% of control from day 3 of pregnancy. At day 16, undernutrition reduced placental, but not fetal, weight in association with decreased junctional zone volume and placental expression of glucose transporter Slc2a1. At day 19, both placental and fetal weights were reduced in undernourished mice (91% and 87% of control, respectively, P < 0.01), as were the volume and surface area of the labyrinthine zone responsible for placental nutrient transfer (85% and 86%, respectively, P < 0.03). However, unidirectional materno-fetal clearance of tracer glucose was maintained and methyl-aminoisobutyric acid increased 166% (P < 0.005) per gram of undernourished placenta, relative to controls. This was associated with an 18% and 27% increased placental expression of glucose and system A amino acid transporters Slc2a1 and Slc38a2, respectively, at day 19 (P < 0.04). At both ages, undernutrition decreased expression of the placental specific transcript of the Igf2 gene by 35% (P < 0.01), although methylation of its promoter was unaffected. The placenta, therefore, adapts to help maintain fetal growth when its own growth is compromised by maternal undernutrition. Consequently, placental phenotype is responsive to environmental conditions and may help predict the risk of adult disease programmed in utero.
妊娠期间营养不良会降低出生体重,并影响成年后的表型,从而影响预期寿命,但它对胎盘表型的影响(胎盘负责为胎儿生长提供营养)在很大程度上仍不清楚。本研究使用分子、形态和功能分析方法,在妊娠第 3 天开始将饮食摄入量限制为对照组的 80%,以检查小鼠胎盘的表型。在第 16 天,与对照组相比,营养不良减少了胎盘(减少了 29%),但不减少胎儿(减少了 9%)的体重,这与胎盘的连接区体积减少和葡萄糖转运蛋白 Slc2a1 的胎盘表达减少有关。在第 19 天,与对照组相比,营养不良的小鼠的胎盘和胎儿的重量均减少(分别减少了 87%和 87%),胎盘营养转运的绒毛膜区的体积和表面积也分别减少了 86%和 86%)(均 P < 0.03)。然而,示踪葡萄糖的单向母体-胎儿清除率保持不变,且甲基丙氨酸的含量增加了 166%(P < 0.005),与对照组相比,每克营养不良的胎盘增加 166%(P < 0.005)。这与葡萄糖和系统 A 氨基酸转运蛋白 Slc2a1 和 Slc38a2 的胎盘表达分别增加 18%和 27%有关(P < 0.04)。在这两个年龄阶段,营养不良导致胎盘特异性 Igf2 基因转录物的表达减少了 35%(P < 0.01),尽管其启动子的甲基化不受影响。因此,当胎盘自身的生长因母体营养不良而受损时,胎盘会适应以帮助维持胎儿的生长。因此,胎盘表型对环境条件有反应,并可能有助于预测宫内编程的成年疾病的风险。