MicroRNA-21 accelerates hepatocyte proliferation in vitro via PI3K/Akt signaling by targeting PTEN

被引:67
|
作者
Bai Yan-nan [1 ,2 ]
Yu Zhao-yan [1 ]
Luo Li-xi [1 ]
Yi Jiang [1 ]
Xia Qing-jie [3 ]
Zeng Yong [1 ]
机构
[1] Sichuan Univ, West China Hosp, Dept Hepatobiliary Pancreat Surg, Chengdu 610041, Sichuan Provinc, Peoples R China
[2] Fujian Med Univ, Prov Clin Coll, Fujian Prov Hosp, Dept Hepatobiliary Surg, Fuzhou 350001, Fujian Province, Peoples R China
[3] Sichuan Univ, West China Med Sch, West China Hosp, Translat Neurosci Ctr, Chengdu 610041, Sichuan Provinc, Peoples R China
关键词
Liver regeneration; Proliferation; microRNA-21; Phosphatase and tensin homologue deleted on chromosome 10; CELL-CYCLE PROGRESSION; LIVER-REGENERATION; PARTIAL-HEPATECTOMY; PROTEIN-KINASE; EXPRESSION; PHASE; CANCER; GENE; ACTIVATION; MECHANISM;
D O I
10.1016/j.bbrc.2013.12.047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
MicroRNAs (miRNAs) are involved in controlling hepatocyte proliferation during liver regeneration. In this study, we established the miRNAs-expression patterns of primary hepatocytes in vitro under stimulation of epidermal growth factor (EGF), and found that microRNA-21 (miR-21) was appreciably up-regulated and peaked at 12 h. In addition, we further presented evidences indicating that miR-21 promotes primary hepatocyte proliferation through in vitro transfecting with miR-21 mimics or inhibitor. We further demonstrated that phosphatidylinositol 3'-OH kinase (PI3K)/Akt signaling was altered accordingly, it is, by targeting phosphatase and tensin homologue deleted on chromosome 10, PI3K/Akt signaling is activated by miR-21 to accelerate hepatocyte rapid S-phase entry and proliferation in vitro. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:802 / 807
页数:6
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