Mir-34a Is Upregulated during Liver Regeneration in Rats and Is Associated with the Suppression of Hepatocyte Proliferation

被引:85
作者
Chen, Huan [1 ]
Sun, Yimin [2 ]
Dong, Ruiqi [1 ]
Yang, Shengsheng [1 ]
Pan, Chuanyong [1 ]
Xiang, Dao [3 ]
Miao, Mingyong [1 ]
Jiao, Binghua [1 ]
机构
[1] Second Mil Med Univ, Dept Biochem & Mol Biol, Shanghai, Peoples R China
[2] Natl Engn Res Ctr Beijing Biochip Technol, Beijing, Peoples R China
[3] Second Mil Med Univ, Dept Cellular Biol, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
TUMOR-SUPPRESSOR; GROWTH-FACTOR; DOWN-REGULATION; CELL LINE; ACTIVIN-B; EXPRESSION; MICRORNAS; BETA; HEPATECTOMY; FOLLISTATIN;
D O I
10.1371/journal.pone.0020238
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
Background: MicroRNAs are a class of small regulatory RNAs that modulate a variety of biological processes, including cellular differentiation, apoptosis, metabolism and proliferation. This study aims to explore the effect of miR-34a in hepatocyte proliferation and its potential role in liver regeneration termination. Methodology/Principal Finding: MiR-34a was highly induced after partial hepatectomy. Overexpression of miR-34a in BRL3A cells could significantly inhibit cell proliferation and down-regulate the expression of inhibin bB (INHBB) and Met. In BRL3A cells, INHBB was identified as a direct target of miR-34a by luciferase reporter assay. More importantly, INHBB siRNA significantly repressed cell proliferation. A decrease of INHBB and Met was detected in regenerating liver. Conclusion/Significance: MiR-34a expression was upregulated during the late phase of liver regeneration. MiR-34amediated regulation of INHBB and Met may collectively contribute to the suppression of hepatocyte proliferation.
引用
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页数:7
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