Genetics and Genomics Group, Sanford Research, Sioux Falls, SD, United States.
Environmental Influences on Health and Disease Group, Sanford Research, Sioux Falls, SD, United States.
Front Endocrinol (Lausanne). 2020 Sep 17;11:570846. doi: 10.3389/fendo.2020.570846. eCollection 2020.
Children born to diabetic or obese mothers have a higher risk of heart disease at birth and later in life. Using chromatin immunoprecipitation sequencing, we previously demonstrated that late-gestation diabetes, maternal high fat (HF) diet, and the combination causes distinct fuel-mediated epigenetic reprogramming of rat cardiac tissue during fetal cardiogenesis. The objective of the present study was to investigate the overall transcriptional signature of newborn offspring exposed to maternal diabetes and maternal H diet. Microarray gene expression profiling of hearts from diabetes exposed, HF diet exposed, and combination exposed newborn rats was compared to controls. Functional annotation, pathway and network analysis of differentially expressed genes were performed in combination exposed and control newborn rat hearts. Further downstream metabolic assessments included measurement of total and phosphorylated AKT2 and GSK3β, as well as quantification of glycolytic capacity by extracellular flux analysis and glycogen staining. Transcriptional analysis identified significant fuel-mediated changes in offspring cardiac gene expression. Specifically, functional pathways analysis identified two key signaling cascades that were functionally prioritized in combination exposed offspring hearts: (1) downregulation of fibroblast growth factor (FGF) activated PI3K/AKT pathway and (2) upregulation of peroxisome proliferator-activated receptor gamma coactivator alpha (PGC1α) mitochondrial biogenesis signaling. Functional metabolic and histochemical assays supported these transcriptome changes, corroborating diabetes- and diet-induced cardiac transcriptome remodeling and cardiac metabolism in offspring. This study provides the first data accounting for the compounding effects of maternal hyperglycemia and hyperlipidemia on the developmental cardiac transcriptome, and elucidates nuanced and novel features of maternal diabetes and diet on regulation of heart health.
患有糖尿病或肥胖症的母亲所生的孩子,在出生时和以后的生活中患心脏病的风险更高。我们之前使用染色质免疫沉淀测序技术证明,妊娠晚期糖尿病、母体高脂肪(HF)饮食以及两者的结合会导致胎儿心脏发生期间大鼠心脏组织发生独特的燃料介导的表观遗传重编程。本研究的目的是研究暴露于母体糖尿病和母体 H 饮食的新生后代的整体转录特征。将糖尿病暴露、HF 饮食暴露和联合暴露的新生大鼠心脏的基因表达谱进行微阵列基因表达谱分析,并与对照进行比较。对联合暴露和对照新生大鼠心脏中差异表达基因进行功能注释、通路和网络分析。进一步的下游代谢评估包括测量总蛋白和磷酸化 AKT2 和 GSK3β,以及通过细胞外通量分析和糖原染色定量测定糖酵解能力。转录分析确定了后代心脏基因表达的显著燃料介导变化。具体而言,功能途径分析确定了联合暴露后代心脏中两个功能优先的关键信号级联:(1)成纤维细胞生长因子(FGF)激活的 PI3K/AKT 途径下调,(2)过氧化物酶体增殖物激活受体 γ 共激活因子α(PGC1α)线粒体生物发生信号上调。功能代谢和组织化学测定支持这些转录组变化,证实了糖尿病和饮食引起的后代心脏转录组重塑和心脏代谢。本研究首次提供了母体高血糖和高血脂对发育中心脏转录组复合影响的数据,并阐明了母体糖尿病和饮食对心脏健康调节的细微和新颖特征。