Das Undurti N, Rao Allam A
UND Life Sciences, 13800 Fairhill Road, #321, Shaker Heights, OH 44120, USA.
Lipids Health Dis. 2007 Dec 14;6:35. doi: 10.1186/1476-511X-6-35.
Obesity is an important component of metabolic syndrome X and predisposes to the development of type 2 diabetes mellitus. The incidence of obesity, type 2 diabetes mellitus and metabolic syndrome X is increasing, and the cause(s) for this increasing incidence is not clear. Although genetics could play an important role in the higher prevalence of these diseases, it is not clear how genetic factors interact with environmental and dietary factors to increase their incidence. We performed gene expression profile in subjects with obesity and type 2 diabetes mellitus with and without family history of these diseases. It was noted that genes involved in carbohydrate, lipid and amino acid metabolism pathways, glycan of biosynthesis, metabolism of cofactors and vitamin pathways, ubiquitin mediated proteolysis, signal transduction pathways, neuroactive ligand-receptor interaction, nervous system pathways, neurodegenerative disorders pathways are upregulated in obesity compared to healthy subjects. In contrast genes involved in cell adhesion molecules, cytokine-cytokine receptor interaction, insulin signaling and immune system pathways are downregulated in obese. Genes involved in signal transduction, regulation of actin cytoskeleton, antigen processing and presentation, complement and coagulation cascades, axon guidance and neurodegenerative disorders pathways are upregulated in subjects with type 2 diabetes with family history of diabetes compared to those who are diabetic but with no family history. Genes involved in oxidative phosphorylation, immune, nervous system, and metabolic disorders pathways are upregulated in those with diabetes with family history of diabetes compared to those with diabetes but with no family history. In contrast, genes involved in lipid and amino acid pathways, ubiquitin mediated proteolysis, signal transduction, insulin signaling and PPAR signaling pathways are downregulated in subjects with diabetes with family history of diabetes. It was noted that genes involved in inflammatory pathway are differentially expressed both in obesity and type 2 diabetes. These results suggest that genes concerned with carbohydrate, lipid and amino acid metabolic pathways, neuronal function and inflammation play a significant role in the pathobiology of obesity and type 2 diabetes.
肥胖是代谢综合征X的重要组成部分,易引发2型糖尿病。肥胖症、2型糖尿病和代谢综合征X的发病率正在上升,而发病率上升的原因尚不清楚。虽然遗传学可能在这些疾病的较高患病率中起重要作用,但尚不清楚遗传因素如何与环境和饮食因素相互作用以增加其发病率。我们对有或无这些疾病家族史的肥胖和2型糖尿病患者进行了基因表达谱分析。结果发现,与健康受试者相比,肥胖患者中参与碳水化合物、脂质和氨基酸代谢途径、聚糖生物合成、辅因子和维生素代谢途径、泛素介导的蛋白水解、信号转导途径、神经活性配体-受体相互作用、神经系统途径、神经退行性疾病途径的基因上调。相比之下,肥胖患者中参与细胞粘附分子、细胞因子-细胞因子受体相互作用、胰岛素信号传导和免疫系统途径的基因下调。与无糖尿病家族史的糖尿病患者相比,有糖尿病家族史的2型糖尿病患者中参与信号转导、肌动蛋白细胞骨架调节、抗原加工和呈递、补体和凝血级联反应、轴突导向和神经退行性疾病途径的基因上调。与无糖尿病家族史的糖尿病患者相比,有糖尿病家族史的糖尿病患者中参与氧化磷酸化、免疫、神经系统和代谢紊乱途径的基因上调。相反,有糖尿病家族史的糖尿病患者中参与脂质和氨基酸途径、泛素介导的蛋白水解、信号转导、胰岛素信号传导和PPAR信号传导途径的基因下调。值得注意的是,参与炎症途径的基因在肥胖和2型糖尿病中均有差异表达。这些结果表明,与碳水化合物、脂质和氨基酸代谢途径、神经元功能和炎症相关的基因在肥胖和2型糖尿病的病理生物学中起重要作用。