MiRNA-21 has effects to protect kidney injury induced by sepsis

被引:39
作者
Fu Dian [1 ]
Dong Jie [1 ]
Li Ping [1 ]
Tang Chaopeng [1 ]
Cheng Wen [1 ]
Xu Zhenyu [1 ]
Zhou Wenquan [1 ]
Ge Jingping [1 ]
Xia Chen [2 ]
Zhang Zhengyu [1 ]
机构
[1] Nanjing Univ, Sch Med, Nanjing Jinling Hosp, Dept Urol, Nanjing 210002, Jiangsu, Peoples R China
[2] Nanjing Med Univ, Childrens Hosp, Nanjing 210000, Jiangsu, Peoples R China
关键词
miRNA-21; Vitro; Vovo; Apoptosis; PTEN; PI3K; AKT; Kidney injury; SIGNALING PATHWAY; APOPTOSIS; MICRORNA-21; MIR-21; CANCER; CELLS; REPERFUSION; EXPRESSION; MECHANISM; TARGETS;
D O I
10.1016/j.biopha.2017.07.098
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
To investigate the miRNA-21 over-expression in the acute kidney injury induced by sepsis, we developed a sepsis induced in vitro model by lip polysaccharide (LPS) and in vovo model by cecal ligation and puncture (CLP) surgery. LPS or CLP surgery induced kidney cell apoptosis increasing. However, the kidney injury indexes of miRNA groups which were transfected with miRNA-21 were significantly suppressed. In further study, the relative proteins expressions were evaluated to explain the miRNA-21 mechanism to improve sepsis induced kidney cell apoptosis. The results were shown that miRNA-21 over-expression had effects to protect kidney cell apoptosis induced by sepsis via PTEN/PI3K/AKT signaling pathway. (C) 2017 Published by Elsevier Masson SAS.
引用
收藏
页码:1138 / 1144
页数:7
相关论文
共 30 条
[1]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[2]   Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers [J].
Calin, GA ;
Sevignani, C ;
Dan Dumitru, C ;
Hyslop, T ;
Noch, E ;
Yendamuri, S ;
Shimizu, M ;
Rattan, S ;
Bullrich, F ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :2999-3004
[3]   MicroRNA signatures in human cancers [J].
Calin, George A. ;
Croce, Carlo M. .
NATURE REVIEWS CANCER, 2006, 6 (11) :857-866
[4]   The PTEN/PI3K/AKT signalling pathway in cancer, therapeutic implications [J].
Carnero, Amancio ;
Blanco-Aparicio, Carmen ;
Renner, Oliver ;
Link, Wolfgang ;
Leal, Juan F. M. .
CURRENT CANCER DRUG TARGETS, 2008, 8 (03) :187-198
[5]   Transforming growth factor-β1 induces epithelial-mesenchymal transition and increased expression of matrix metalloproteinase-16 via miR-200b downregulation in bladder cancer cells [J].
Chen, Min Feng ;
Zeng, Feng ;
Qi, Lin ;
Zui, Xiong Bing ;
Wang, Jun ;
Liu, Long Fei ;
Li, Yuan .
MOLECULAR MEDICINE REPORTS, 2014, 10 (03) :1549-1554
[6]   Most mammalian mRNAs are conserved targets of microRNAs [J].
Friedman, Robin C. ;
Farh, Kyle Kai-How ;
Burge, Christopher B. ;
Bartel, David P. .
GENOME RESEARCH, 2009, 19 (01) :92-105
[7]   MiR-21 mediates sorafenib resistance of hepatocellular carcinoma cells by inhibiting autophagy via the PTEN/Akt pathway [J].
He, Changjun ;
Dong, Xuesong ;
Zhai, Bo ;
Jiang, Xian ;
Dong, Deli ;
Li, Baoxin ;
Jiang, Hongchi ;
Xu, Shidong ;
Sun, Xueying .
ONCOTARGET, 2015, 6 (30) :28867-28881
[8]   Ursolic acid induced anti-proliferation effects in rat primary vascular smooth muscle cells is associated with inhibition of microRNA-21 and subsequent PTEN/113K [J].
Jiang, Qixiao ;
Han, Yantao ;
Gao, Hui ;
Tian, Rong ;
Li, Ping ;
Wang, Chunbo .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2016, 781 :69-75
[9]  
Johnson SM, 2005, CELL, V120, P635, DOI 10.1016/j.cell.2005.01.014
[10]   PTEN enhances TNF-induced apoptosis through modulation of nuclear factor-κB signaling pathway in human glioma cells [J].
Koul, Dimpy ;
Takada, Yasunari ;
Shen, Ruijun ;
Aggarwal, Bharat B. ;
Yung, W. K. Alfred .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 350 (02) :463-471