Zhang Haojun, Zhao Tingting, Li Zhiguo, Yan Meihua, Zhao Hailing, Zhu Bin, Li Ping
Beijing Key Lab Immune-Mediated Inflammatory Diseases, Institute of Clinical Medical Sciences, China-Japan Friendship Hospital, Beijing, China.
Department of Medical Research Center, International Science and Technology Cooperation Base of Geriatric Medicine, North China University of Science and Technology, Tangshan, China.
J Diabetes Res. 2017;2017:8391253. doi: 10.1155/2017/8391253. Epub 2017 Jan 23.
Diabetic nephropathy (DN), a common diabetic microvascular complication, is characterized by progressive glomerular sclerosis and tubulointerstitial fibrosis. However, the underlying mechanisms involved in DN remain to be elucidated. We explored changes in the transcriptional profile in spontaneous type 2 diabetic db/db mice by using the cDNA microarray. Compared with control db/m mice, the db/db mice exhibited marked increases in body weight, kidney weight, and urinary albumin excretion. Renal histological analysis revealed mesangial expansion and thickness of the basement membrane in the kidney of the db/db mice. A total of 355 differentially expressed genes (DEGs) were identified by microarray analysis. Pathway enrichment analysis suggested that biological oxidation, bile acid metabolism, and steroid hormone synthesis were the 3 major significant pathways. The top 10 hub genes were selected from the constructed PPI network of DEGs, including and , which remained largely unclear in DN. We believe that our study can help elucidate the molecular mechanisms underlying DN.
糖尿病肾病(DN)是一种常见的糖尿病微血管并发症,其特征为进行性肾小球硬化和肾小管间质纤维化。然而,DN所涉及的潜在机制仍有待阐明。我们通过使用cDNA微阵列探索了自发性2型糖尿病db/db小鼠转录谱的变化。与对照db/m小鼠相比,db/db小鼠的体重、肾脏重量和尿白蛋白排泄显著增加。肾脏组织学分析显示db/db小鼠肾脏中系膜扩张和基底膜增厚。通过微阵列分析鉴定出总共355个差异表达基因(DEG)。通路富集分析表明生物氧化、胆汁酸代谢和类固醇激素合成是3条主要的显著通路。从构建的DEG的蛋白质-蛋白质相互作用(PPI)网络中选择了前10个枢纽基因,包括 和 ,它们在DN中很大程度上仍不清楚。我们相信我们的研究有助于阐明DN潜在的分子机制。