Non-genetic mechanisms of diabetic nephropathy

被引:51
|
作者
Han, Qiuxia [1 ,2 ]
Zhu, Hanyu [1 ]
Chen, Xiangmei [1 ]
Liu, Zhangsuo [2 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Chinese PLA Inst Nephrol, Natl Clin Res Ctr Kidney Dis,Dept Nephrol, State Key Lab Kidney Dis,Beijing Key Lab Kidney D, Beijing 100853, Peoples R China
[2] Zhengzhou Univ, Affiliated Hosp 1, Dept Nephrol, Zhengzhou 450052, Henan, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
diabetic nephropathy; immune inflammatory response; epithelial-mesenchymal transition; apoptosis; mitochondrial damage; epigenetics; podocyte-endothelial communication; EPITHELIAL-MESENCHYMAL TRANSITION; ENDOPLASMIC-RETICULUM STRESS; PROMOTES RENAL FIBROSIS; MANNOSE-BINDING LECTIN; TOLL-LIKE RECEPTORS; VITAMIN-D-RECEPTOR; INOSITOL 1,4,5-TRISPHOSPHATE; NLRP3; INFLAMMASOME; VASCULAR COMPLICATIONS; ENDOTHELIAL GLYCOCALYX;
D O I
10.1007/s11684-017-0569-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Diabetic nephropathy (DN) is one of the most common microvascular complications in diabetes mellitus patients and is characterized by thickened glomerular basement membrane, increased extracellular matrix formation, and podocyte loss. These phenomena lead to proteinuria and altered glomerular filtration rate, that is, the rate initially increases but progressively decreases. DN has become the leading cause of end-stage renal disease. Its prevalence shows a rapid growth trend and causes heavy social and economic burden in many countries. However, this disease is multifactorial, and its mechanism is poorly understood due to the complex pathogenesis of DN. In this review, we highlight the new molecular insights about the pathogenesis of DN from the aspects of immune inflammation response, epithelial-mesenchymal transition, apoptosis and mitochondrial damage, epigenetics, and podocyte-endothelial communication. This work offers groundwork for understanding the initiation and progression of DN, as well as provides ideas for developing new prevention and treatment measures.
引用
收藏
页码:319 / 332
页数:14
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