Mir-34a is upregulated during liver regeneration in rats and is associated with the suppression of hepatocyte proliferation.

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 regene...

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Main Authors: Huan Chen, Yimin Sun, Ruiqi Dong, Shengsheng Yang, Chuanyong Pan, Dao Xiang, Mingyong Miao, Binghua Jiao
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3105003?pdf=render
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spelling doaj-262d7f8e7340484a907675822b0d1b512020-11-24T21:26:36ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0165e2023810.1371/journal.pone.0020238Mir-34a is upregulated during liver regeneration in rats and is associated with the suppression of hepatocyte proliferation.Huan ChenYimin SunRuiqi DongShengsheng YangChuanyong PanDao XiangMingyong MiaoBinghua JiaoBACKGROUND: 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 BRL-3A cells could significantly inhibit cell proliferation and down-regulate the expression of inhibin βB (INHBB) and Met. In BRL-3A 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-34a-mediated regulation of INHBB and Met may collectively contribute to the suppression of hepatocyte proliferation.http://europepmc.org/articles/PMC3105003?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Huan Chen
Yimin Sun
Ruiqi Dong
Shengsheng Yang
Chuanyong Pan
Dao Xiang
Mingyong Miao
Binghua Jiao
spellingShingle Huan Chen
Yimin Sun
Ruiqi Dong
Shengsheng Yang
Chuanyong Pan
Dao Xiang
Mingyong Miao
Binghua Jiao
Mir-34a is upregulated during liver regeneration in rats and is associated with the suppression of hepatocyte proliferation.
PLoS ONE
author_facet Huan Chen
Yimin Sun
Ruiqi Dong
Shengsheng Yang
Chuanyong Pan
Dao Xiang
Mingyong Miao
Binghua Jiao
author_sort Huan Chen
title Mir-34a is upregulated during liver regeneration in rats and is associated with the suppression of hepatocyte proliferation.
title_short Mir-34a is upregulated during liver regeneration in rats and is associated with the suppression of hepatocyte proliferation.
title_full Mir-34a is upregulated during liver regeneration in rats and is associated with the suppression of hepatocyte proliferation.
title_fullStr Mir-34a is upregulated during liver regeneration in rats and is associated with the suppression of hepatocyte proliferation.
title_full_unstemmed Mir-34a is upregulated during liver regeneration in rats and is associated with the suppression of hepatocyte proliferation.
title_sort mir-34a is upregulated during liver regeneration in rats and is associated with the suppression of hepatocyte proliferation.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description 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 BRL-3A cells could significantly inhibit cell proliferation and down-regulate the expression of inhibin βB (INHBB) and Met. In BRL-3A 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-34a-mediated regulation of INHBB and Met may collectively contribute to the suppression of hepatocyte proliferation.
url http://europepmc.org/articles/PMC3105003?pdf=render
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