Human umbilical cord mesenchymal stem cell attenuates renal fibrosis via TGF-β/Smad signaling pathways in vivo and in vitro

被引:15
|
作者
Yu, Yihang [1 ,2 ,3 ,4 ,5 ,6 ]
Hu, Dong [1 ,2 ,3 ,4 ,5 ,6 ]
Zhou, Yu [1 ,2 ,3 ,4 ,5 ,6 ]
Xiang, Han [1 ,2 ,3 ,4 ,5 ,6 ]
Liu, Bo [1 ,2 ,3 ,4 ,5 ,6 ]
Shen, Lianju [1 ,2 ,3 ,4 ,5 ,6 ]
Long, Chunlan [1 ,2 ,3 ,4 ,5 ,6 ]
Liu, Xing [1 ,2 ,3 ,4 ,5 ,6 ]
Lin, Tao [1 ,2 ,3 ,4 ,5 ,6 ]
He, Dawei [1 ,2 ,3 ,4 ,5 ,6 ]
Zhang, Yuanyuan [7 ]
Xu, Tao [8 ]
Zhang, Deying [1 ,2 ,3 ,4 ,5 ,6 ]
Wei, Guanghui [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Chongqing Med Univ, Childrens Hosp, Dept Urol, Chongqing 400014, Peoples R China
[2] Chongqing Key Lab Children Urogenital Dept & Tiss, Chongqing 400014, Peoples R China
[3] Minist Educ, Key Lab Child Dev & Disorders, Chongqing 400014, Peoples R China
[4] China Int Sci & Technol Cooperat Base Child Dev &, Chongqing 400014, Peoples R China
[5] Natl Clin Res Ctr Child Hlth & Disorders, Chongqing 400014, Peoples R China
[6] Chongqing Key Lab Pediat, Chongqing 400014, Peoples R China
[7] Wake Forest Sch Med, Wake Forest Inst Regenerat Med, Winston Salem, NC 27101 USA
[8] Tsinghua Univ, Biomfg Ctr, Dept Mech Engn, Beijing 100084, Peoples R China
关键词
Mesenchymal stem cell; Renal fibrosis; Epithelial to mesenchymal transition; TGE-beta/Smad signaling pathway; Aristolochic acid; ARISTOLOCHIC ACID NEPHROPATHY; TRANSITION; THERAPY; TRANSPLANTATION; MECHANISMS; RELEVANCE; BETA; MICE;
D O I
10.1016/j.ejphar.2020.173343
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Renal fibrosis is a progressive pathological process that eventually leads to end-stage renal failure with limited therapeutic options. The aim of this study was to investigate the nephron-protective effect of human umbilical cord mesenchymal stem cells (ucMSCs) on renal fibrosis. UcMSCs were intravenously injected into renal fibrosis mice induced by aristolochic acid (AA) and co-cultured with HK-2 cells induced by TGF-beta 1, respectively. The kidney functions including serum creatinine (Scr) and blood urea nitrogen (BUN) levels, and histopathology were examined after treated with stem cells and normal saline as control. Immunohistochemical staining, immunofluorescent staining, and Western blot analysis were used to assessed the expression of proteins associated with epithelial to mesenchymal transition (EMT) and TGF-beta/Smad signaling pathway. The results showed that ucMSCs effectively improved the kidney function and pathological structure, reduced AA-induced fibrosis and extracellular matrix deposition. Besides, UcMSCs significantly inhibited the EMT process and TGF-beta/Smad signaling pathway in AA-induced mice and TGF-beta 1-induced HK-2 cells compared to the control (p < 0.05). Our data suggested that ucMSCs play as a nephmn-protective role in anti-fibrosis through inhibiting the activation of TGF-beta/Smad signaling pathway.
引用
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页数:8
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