Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10870655 | FEBS Letters | 2013 | 10 Pages |
Abstract
In our previous study, miR-126 was identified as one of the leading miRNAs that is downregulated during activation of hepatic stellate cells (HSCs). However, the roles and related mechanisms of miR-126 in HSCs are not understood. In this study, we compared expression of miR-126 during HSC activation both in vitro and in vivo. We also applied RNA interference to analyze the role and mechanism of miR-126â in the activation of HSCs. Restoring HSCs with Lv-miR-126â resulted in decreased proliferation, accumulation of extracellular matrix components, and cell contraction, while also negatively regulating the vascular endothelial growth factor (VEGF) signal transduction pathways by partially targeted VEGF-A. Thus, we postulate that miR-126 may be a biological marker for the activation of HSCs, and useful for reducing intrahepatic vascular resistance and improving the sinusoidal microcirculation in chronic liver diseases.
Keywords
ECMVEGFAKEGGPI3KCol IVHSCEGFL73′untranslated region3′UTRAktChronic liver diseaseKyoto Encyclopedia of Genes and GenomesHepatic stellate cellVascular endothelial growth factorVascular Endothelial Growth Factor (VEGF)phosphatidylinositol-3-kinaseLamininExtracellular matrixMicroRNAMiRNAType IV collagenGene ontologyhematoxylin/eosinPortal hypertensionprotein kinase B
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Authors
Can-Jie Guo, Qin Pan, Hua Xiong, Yu-Qi Qiao, Zhao-Lian Bian, Wei Zhong, Li Sheng, Hai Li, Lei Shen, Jing Hua, Xiong Ma, Jing-Yuan Fang,