Chriett Sabrina, Le Huërou-Luron Isabelle, Vidal Hubert, Pirola Luciano
Carmen (Cardiology, Metabolism and Nutrition) Laboratory, INSERM U1060, Lyon-1 University, South Lyon Medical Faculty, 69921 Oullins, France.
INRA - UR 1341 ADNC, 35590 Saint-Gilles, France.
Gen Comp Endocrinol. 2016 Jun 1;232:76-85. doi: 10.1016/j.ygcen.2015.12.028. Epub 2016 Jan 6.
Prenatal and early postnatal life determines future health, and intrauterine growth restriction (IUGR) - associated low birth weight predisposes to metabolic syndrome in adulthood. We hypothesize here that IUGR might induce hormonal and gene expression alterations predisposing to metabolic disease. Using a porcine model of spontaneous IUGR, we determined in utero (71, 112days post-conception) and early-postnatal (2days post-birth) IGF-1, insulin and leptin levels, and in parallel we investigated, in skeletal muscle, the developmental expression patterns of sirtuins and metabolic and signaling genes IRS1, GLUT4, HK2 and GAPDH. IUGR was associated with impaired IGF-1 plasmatic levels. Gene expression of sirtuin 1, 5, 6, 7, GLUT4 and HK2 exhibited significant correlations with gestational age or body weight. SIRT1 and HK2 expression displayed an age- and weight-dependent downregulation in controls, which was lost in IUGR pigs. Conversely, SIRT2 and GLUT4 were upregulated in IUGR pigs. Within the set of genes studied, we found a significant correlation between IGF-1 levels and gene expression in control, but not IUGR samples, indicating that lower IGF-1 may be a limiting factor in IUGR. IUGR-dependent gene alterations were partly linked to epigenetic changes on histone H3 acetylation and methylation. Overall, our data indicate that several sirtuins and metabolic genes display specific gene expression trajectories during fetal and early postnatal life. Gene expression alterations observed in IUGR are correlated to IGF-1 dysregulation. Given the importance of the genes studied in metabolic control, their perinatal alterations might contribute to the predisposition to metabolic disease of adulthood.
产前和产后早期生活决定未来健康,与宫内生长受限(IUGR)相关的低出生体重易导致成年期代谢综合征。我们在此假设,IUGR可能会诱导激素和基因表达改变,从而易患代谢性疾病。利用自发性IUGR的猪模型,我们测定了子宫内(受孕后71、112天)和出生后早期(出生后2天)的IGF-1、胰岛素和瘦素水平,同时我们研究了骨骼肌中沉默调节蛋白、代谢和信号基因IRS1、GLUT4、HK2和GAPDH的发育表达模式。IUGR与IGF-1血浆水平受损有关。沉默调节蛋白1、5、6、7、GLUT4和HK2的基因表达与胎龄或体重呈显著相关性。在对照组中,SIRT1和HK2表达呈现年龄和体重依赖性下调,而在IUGR猪中则消失。相反,SIRT2和GLUT4在IUGR猪中上调。在所研究的基因组中,我们发现对照组而非IUGR样本中IGF-1水平与基因表达之间存在显著相关性,这表明较低的IGF-1可能是IUGR中的一个限制因素。IUGR依赖性基因改变部分与组蛋白H3乙酰化和甲基化的表观遗传变化有关。总体而言,我们的数据表明,几种沉默调节蛋白和代谢基因在胎儿期和出生后早期生活中显示出特定的基因表达轨迹。在IUGR中观察到的基因表达改变与IGF-1失调相关。鉴于所研究的基因在代谢控制中的重要性,它们在围产期的改变可能有助于成年期代谢性疾病的易感性。