MircoRNA-145 promotes activation of hepatic stellate cells via targeting kruppel-like factor 4

被引:23
|
作者
Men, Ruoting [1 ,2 ]
Wen, Maoyao [1 ]
Zhao, Mingyue [3 ]
Dan, Xuelian [1 ]
Yang, Zongze [4 ]
Wu, Wenchao [3 ]
Wang, Maggie Haitian [2 ]
Liu, Xiaojing [3 ]
Yang, Li [1 ]
机构
[1] Sichuan Univ, West China Hosp, Div Gastroenterol & Hepatol, Chengdu 610041, Peoples R China
[2] Chinese Univ Hong Kong, Fac Med, JC Sch Publ Hlth & Primary Care, Dept Biostat, Hong Kong, Hong Kong, Peoples R China
[3] Sichuan Univ, West China Hosp, Regenerat Med Res Ctr, Lab Cardiovasc Dis, Chengdu 610041, Peoples R China
[4] Sichuan Univ, West China Hosp, Creat & Management Tumour Bank, Chengdu 610041, Sichuan, Peoples R China
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
基金
中国国家自然科学基金;
关键词
GROWTH-FACTOR-BETA; MIR-145; DIFFERENTIATION; PROLIFERATION; FIBROSIS; KLF4; EXPRESSION; MICRORNAS; REGULATOR; PHENOTYPE;
D O I
10.1038/srep40468
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Kruppel-like Factor 4 (KLF4), a target gene of miR-145, can negatively regulate lung fibrosis. However, the potential role of KLF4 and miR-145 in hepatic stellate cells (HSCs) activation or in hepatic fibrosis keeps unclear. This study aims to characterize miR-145 and KLF4 in activated HSCs and liver cirrhotic, and the underlying molecular basis. miR-145 was significantly up-regulated, while KLF4 was dramatically down-regulated during the activation of rat primary HSCs and TGF-beta treated HSCs. Furthermore, miR-145 mimics induced and inhibition of miR-145 reduced a-SMA and COL-I expression in primary HSCs. Additionally, the mRNA and protein levels of KLF4 in the liver of cirrhotic patients and rats were significantly down-regulated. alpha-SMA and COL-I were increased after inhibition of KLF4 by specific shRNA in primary HSCs. Forced KLF4 expression led to a reduction of a-SMA and COL-I expression in HSCs. miR-145 promotes HSC activation and liver fibrosis by targeting KLF4.
引用
收藏
页数:10
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