Edlow Andrea G, Guedj Faycal, Pennings Jeroen L A, Sverdlov Deanna, Neri Caterina, Bianchi Diana W
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Tufts Medical Center, Boston, MA; Mother Infant Research Institute, Tufts Medical Center, Boston, MA.
Mother Infant Research Institute, Tufts Medical Center, Boston, MA.
Am J Obstet Gynecol. 2016 May;214(5):623.e1-623.e10. doi: 10.1016/j.ajog.2016.02.054. Epub 2016 Mar 3.
Maternal obesity is associated with adverse neurodevelopmental outcomes in children, including autism spectrum disorders, developmental delay, and attention-deficit hyperactivity disorder. The underlying mechanisms remain unclear. We previously identified second-trimester amniotic fluid and term cord blood gene expression patterns suggesting dysregulated brain development in fetuses of obese compared with lean women.
We sought to investigate the biological significance of these findings in a mouse model of maternal diet-induced obesity. We evaluated sex-specific differences in fetal growth, brain gene expression signatures, and associated pathways.
Female C57BL/6J mice were fed a 60% high-fat diet or 10% fat control diet for 12-14 weeks prior to mating. During pregnancy, obese dams continued on the high-fat diet or transitioned to the control diet. Lean dams stayed on the control diet. On embryonic day 17.5, embryos were weighed and fetal brains were snap frozen. RNA was extracted from male and female forebrains (10 per diet group per sex) and hybridized to whole-genome expression arrays. Significantly differentially expressed genes were identified using a Welch's t test with the Benjamini-Hochberg correction. Functional analyses were performed using ingenuity pathways analysis and gene set enrichment analysis.
Embryos of dams on the high-fat diet were significantly smaller than controls, with males more severely affected than females (P = .01). Maternal obesity and maternal obesity with dietary change in pregnancy resulted in significantly more dysregulated genes in male vs female fetal brains (386 vs 66, P < .001). Maternal obesity with and without dietary change in pregnancy was associated with unique brain gene expression signatures for each sex, with an overlap of only 1 gene. Changing obese dams to a control diet in pregnancy resulted in more differentially expressed genes in the fetal brain than maternal obesity alone. Functional analyses identified common dysregulated pathways in both sexes, but maternal obesity and maternal dietary change affected different aspects of brain development in males compared with females.
Maternal obesity is associated with sex-specific differences in fetal size and fetal brain gene expression signatures. Male fetal growth and brain gene expression may be more sensitive to environmental influences during pregnancy. Maternal diet during pregnancy has a significant impact on the embryonic brain transcriptome. It is important to consider both fetal sex and maternal diet when evaluating the effects of maternal obesity on fetal neurodevelopment.
母亲肥胖与儿童不良神经发育结局相关,包括自闭症谱系障碍、发育迟缓及注意力缺陷多动障碍。其潜在机制尚不清楚。我们之前鉴定了孕中期羊水和足月脐带血基因表达模式,提示肥胖女性胎儿的脑发育失调,而瘦女性胎儿的脑发育正常。
我们试图在母亲饮食诱导肥胖的小鼠模型中研究这些发现的生物学意义。我们评估了胎儿生长、脑基因表达特征及相关通路中的性别特异性差异。
在交配前,给雌性C57BL/6J小鼠喂食60%高脂肪饮食或10%脂肪对照饮食12 - 14周。在怀孕期间,肥胖的母鼠继续食用高脂肪饮食或转换为对照饮食。瘦母鼠继续食用对照饮食。在胚胎第17.5天,对胚胎称重并将胎儿脑速冻。从雄性和雌性前脑提取RNA(每个饮食组每种性别10个样本),并与全基因组表达阵列杂交。使用经Benjamini - Hochberg校正的Welch's t检验鉴定显著差异表达基因。使用 Ingenuity Pathways Analysis和基因集富集分析进行功能分析。
食用高脂肪饮食的母鼠所产胚胎明显小于对照组,雄性受影响比雌性更严重(P = 0.01)。母亲肥胖以及孕期饮食改变的母亲肥胖导致雄性胎儿脑与雌性胎儿脑中失调基因显著更多(分别为386个和66个,P < 0.001)。孕期母亲肥胖且有或无饮食改变与每种性别的独特脑基因表达特征相关,仅1个基因重叠。孕期将肥胖母鼠转换为对照饮食导致胎儿脑中差异表达基因比单纯母亲肥胖更多。功能分析确定了两性中常见的失调通路,但母亲肥胖和母亲饮食改变对雄性脑发育的影响与对雌性脑发育的影响不同。
母亲肥胖与胎儿大小及胎儿脑基因表达特征中的性别特异性差异相关。雄性胎儿生长和脑基因表达在孕期可能对环境影响更敏感。孕期母亲饮食对胚胎脑转录组有显著影响。在评估母亲肥胖对胎儿神经发育的影响时,考虑胎儿性别和母亲饮食都很重要。