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在早期糖尿病肾病中,Swiprosin-1通过P38丝裂原活化蛋白激酶途径促进肾小球足细胞的线粒体依赖性凋亡。

Swiprosin-1 Promotes Mitochondria-Dependent Apoptosis of Glomerular Podocytes via P38 MAPK Pathway in Early-Stage Diabetic Nephropathy.

作者信息

Wang Rong-Mei, Wang Zhi-Bin, Wang Yue, Liu Wei-Ye, Li Ya, Tong Ling-Chang, Zhang Su, Su Ding-Feng, Cao Yong-Bing, Li Ling, Zhang Li-Chao

机构信息

Department of Pharmacy, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai, China.

Department of Pharmacology, College of Pharmacy, Second Military Medical University, Shanghai, China.

出版信息

Cell Physiol Biochem. 2018;45(3):899-916. doi: 10.1159/000487285. Epub 2018 Feb 2.

Abstract

BACKGROUND/AIMS: Podocyte injury, especially podocyte apoptosis, plays a major role in early-stage diabetic nephropathy (DN). Swiprosin-1, also known as EF hand domain containing 2 (EFhd2), is a Ca2+-binding protein in different cell types. However, the function of swiprosin-1 in podocytes remains unknown.

METHODS

The expression and distribution of swiprosin-1 were investigated in the mouse renal glomerulus and conditionally immortalized mouse podocyte cell line MPC-5. The expression of swiprosin-1 was also detected in streptozotocin (STZ)-treated mice and MPC-5 cells treated with high glucose (HG). Nephrin and podocin were detected by immunohistochemistry and immunofluroscence. Collagen IV, transforming growth factor-β (TGF-β) and fibronectin mRNA expressions were assayed by real-time PCR. Apoptotic proteins and phosphorylation of p38 mitogen-activated protein kinase (MAPK) were detected by immunoblotting.

RESULTS

Swiprosin-1 was found to be expressed in podocytes of the mouse glomerulus and MPC-5 cells. Swiprosin-1 expression was increased in STZ-treated mice and MPC-5 cells treated with HG. In Swiprosin-1-/- diabetic mice, kidney/ body weight, urinary albumin, podocyte foot process effacement and glomerular basement membrane thickening were attenuated; the downregulation of nephrin and podocin expression in the glomerulus was inhibited; and the upregulation of collagen IV, TGF-β and fibronectin mRNA expression in the renal cortex was ameliorated as compared with those in diabetic swiprosin-1+/+ mice. In addition, the increased apoptosis of podocytes, proapoptotic protein expression and p38 phosphorylation in Swiprosin-1-/- diabetic mice were inhibited as compared with those in diabetic swiprosin-1+/+ mice. Knockdown of swiprosin-1 in MPC-5 cells reduced the apoptosis of podocytes, proapoptotic protein expression and p38 phosphorylation induced by HG. Targeted knockdown of p38 attenuated the increased apoptosis of MPC-5 cells over-expressing swiprosin-1.

CONCLUSION

Swiprosin-1 expression in podocytes of the mouse glomerulus played a critical role in early-stage DN. Swiprosin-1 deficiency in early DN attenuated mitochondria-dependent podocyte apoptosis induced by hyperglycemia or HG via p38 MAPK signaling pathway.

摘要

背景/目的:足细胞损伤,尤其是足细胞凋亡,在早期糖尿病肾病(DN)中起主要作用。Swiprosin-1,也称为含EF手结构域蛋白2(EFhd2),是一种在不同细胞类型中表达的Ca2+结合蛋白。然而,Swiprosin-1在足细胞中的功能尚不清楚。

方法

研究Swiprosin-1在小鼠肾小球和条件永生化小鼠足细胞系MPC-5中的表达和分布。还检测了链脲佐菌素(STZ)处理的小鼠和高糖(HG)处理的MPC-5细胞中Swiprosin-1的表达。通过免疫组织化学和免疫荧光检测Nephrin和Podocin。通过实时PCR检测IV型胶原、转化生长因子-β(TGF-β)和纤连蛋白mRNA的表达。通过免疫印迹检测凋亡蛋白和p38丝裂原活化蛋白激酶(MAPK)的磷酸化。

结果

发现Swiprosin-1在小鼠肾小球足细胞和MPC-5细胞中表达。在STZ处理的小鼠和HG处理的MPC-5细胞中,Swiprosin-1表达增加。在Swiprosin-1基因敲除的糖尿病小鼠中,肾重/体重、尿白蛋白、足细胞足突消失和肾小球基底膜增厚减轻;肾小球中Nephrin和Podocin表达的下调受到抑制;与糖尿病Swiprosin-1+/+小鼠相比,肾皮质中IV型胶原、TGF-β和纤连蛋白mRNA表达的上调得到改善。此外,与糖尿病Swiprosin-1+/+小鼠相比,Swiprosin-1基因敲除的糖尿病小鼠中足细胞凋亡增加、促凋亡蛋白表达和p38磷酸化受到抑制。在MPC-5细胞中敲低Swiprosin-1可减少HG诱导的足细胞凋亡、促凋亡蛋白表达和p38磷酸化。靶向敲低p38可减轻过表达Swiprosin-1的MPC-5细胞凋亡增加。

结论

小鼠肾小球足细胞中Swiprosin-1的表达在早期DN中起关键作用。早期DN中Swiprosin-1缺乏通过p38 MAPK信号通路减轻高血糖或HG诱导的线粒体依赖性足细胞凋亡。

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