Netrin-1 attenuates the progression of renal dysfunction by blocking endothelial-to-mesenchymal transition in the 5/6 nephrectomy rat model

• Published in: BMC nephrology Vol. 17; no. 1; p. 47
• Main Authors: Bai, Jiuxu, Hao, Junfeng, Zhang, Xiaoling, Cui, Hanmin, Han, Jingming, Cao, Ning
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 12.05.2016; BioMed Central
• Subjects: Actins - genetics; Actins - metabolism; Animals; Blood Urea Nitrogen; Care and treatment; Chronic kidney failure; Complications and side effects; Creatinine - blood; Endothelium - physiopathology; Epithelial-Mesenchymal Transition - genetics; Fibrosis; Health aspects; Kidney - pathology; Male; Nephrectomy; Netrin-1 - genetics; Netrin-1 - metabolism; Platelet Endothelial Cell Adhesion Molecule-1 - genetics; Platelet Endothelial Cell Adhesion Molecule-1 - metabolism; Prognosis; Rats; Rats, Sprague-Dawley; Renal Insufficiency, Chronic - pathology; Renal Insufficiency, Chronic - physiopathology; RNA, Messenger - metabolism; Signal Transduction; Snail Family Transcription Factors - genetics; Stem cell research; Transforming Growth Factor beta - metabolism; Renal interstitial fibrosis; Endothelial-to-mesenchymal transition; 5/6 Nephrectomized rats; Netrin-1
• ISSN: 1471-2369; 1471-2369
• DOI: 10.1186/s12882-016-0260-4

Endothelial-to-mesenchymal transition (EndoMT) is a crucial event during kidney interstitial fibrosis and it is believed to be inhibited by netrin-1. Our aim was to determine the influence of netrin-1 on renal EndoMT in chronic kidney disease by studying its effect in 5/6 nephrectomized (Nx) rats. Male Sprague-Dawley rats were divided into three groups (10 rats/group): sham-operated rats treated with control adenovirus; 5/6 Nx rats treated with control adenovirus; and 5/6 Nx rats treated with recombinant adenovirus expressing the netrin-1 gene (Ad-netrin-1). Rats were sacrificed 13 weeks after surgery. Blood urea nitrogen (BUN) and serum creatinine (Scr) levels were measured regularly after surgery. After the rats were sacrificed, pathological changes in renal tissues were analyzed histologically. Immunofluorescence was performed to evaluate the co-expression of CD31 and α-SMA. CD31, α-SMA and Snail mRNA were detected by RT-PCR. Protein expression was detected by western blot. Renal function and histopathological damage were significantly improved in Ad-netrin-1-treated 5/6 Nx rats. In the sham and control-treated 5/6 Nx rats, the percentage of CD31(+)/α-SMA(+) cells increased, which indicated EndoMT. However, the percentage of CD31(+)/α-SMA(+) cells were reduced in the netrin-1-treated 5/6 Nx rats, which indicates netrin-1-induced blocking of EndoMT. From the results, it seems that netrin-1 attenuates the progression of renal dysfunction by inhibiting EndoMT in 5/6 Nx rats. Netrin-1 can therefore be considered as a potential therapeutic agent for the treatment of renal fibrosis.