Down-regulation of IRAK1 attenuates podocyte apoptosis in diabetic nephropathy through PI3K/Akt signaling pathway

被引:37
|
作者
Zhang, Yuan [1 ]
Chen, Xiangfan [2 ]
Yuan, Li [1 ]
Zhang, Yide [1 ]
Wu, Jianhua [1 ]
Guo, Naifeng [1 ]
Chen, Xu [1 ]
Liu, Jing [1 ]
机构
[1] Nantong Univ, Dept Nephrol, Affiliated Hosp, 20 Xisi Rd, Nantong 226000, Peoples R China
[2] Nantong Univ, Dept Pharmacol, Sch Med, Nantongs 226000, Peoples R China
基金
国家重点研发计划;
关键词
Interleukin 1 receptor associated kinases; Diabetic nephropathy (DN); Podocyte; Apoptosis; PI3K/Akt; INFLAMMATION; SUPPRESSION; NEPHRIN; INJURY;
D O I
10.1016/j.bbrc.2018.09.175
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetic nephropathy (DN) is one of the most common microvascular complications of diabetes mellitus and often results in chronic renal failure. Here, we found that Interleukin 1 receptor associated kinases (IRAK1) was up-regulated in kidney in both DN patients and high-fat diet (HFD)/streptozotocin (STZ)-induced diabetic mice. In vivo, down regulation of IRAK1 ameliorated renal injury and function, with lower podocyte apoptosis, increased expression of Nephrin, attenuated thickness of the glomerular basement membrane and podocyte footprocess effacement. Furthermore, in vitro, down regulation of IRAK1 in podocytes treated with high glucose (HG), podocyte apoptosis and inflammatory cytokines were significantly decreased, but Nephrin increased. Meanwhile, apoptosis-related genes caspase-3/-9 were inhibited and phosphorylation levels of PI3K/Akt were dramatically down regulated. Thus, IRAK1 is one of the critical components involved in podocyte apoptosis in DN. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:529 / 535
页数:7
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