Role of Epimorphin in Bile Duct Formation of Rat Liver Epithelial Stem-Like Cells: Involvement of Small G Protein RhoA and C/EBPβ

被引:12
作者
Jia, Yali [1 ]
Yao, Hailei [1 ]
Zhou, Junnian [1 ]
Chen, Lin [1 ]
Zeng, Quan [1 ]
Yuan, Hongfeng [1 ]
Shi, Lei [1 ]
Nan, Xue [1 ]
Wang, Yunfang [1 ]
Yue, Wen [1 ]
Pei, Xuetao [1 ]
机构
[1] Beijing Inst Transfus Med, Stem Cell & Regenerat Med Lab, Beijing 100850, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
GLUTAMYL-TRANSPEPTIDASE GENE; DIFFERENTIATION; EXPRESSION; PROMOTER; BILIARY; ADHESION; HEPATOBLASTS; GROWTH; INACTIVATION; GLUTATHIONE;
D O I
10.1002/jcp.22625
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epimorphin/syntaxin 2 is a high conserved and very abundant protein involved in epithelial morphogenesis in various organs. We have shown recently that epimorphin (EPM), a protein exclusively expressed on the surface of hepatic stellate cells and myofibroblasts of the liver, induces bile duct formation of hepatic stem-like cells (WB-F344 cells) in a putative biophysical way. Therefore, the aim of this study was to present some of the molecular mechanisms by which EPM mediates bile duct formation. We established a biliary differentiation model by co-culture of EPM-overexpressed mesenchymal cells (PT67(EPM)) with WB-F344 cells. Here, we showed that EPM could promote WB-F344 cells differentiation into bile duct-like structures. Biliary differentiation markers were also elevated by EPM including Yp, Cx43, aquaporin-1, CK19, and gamma glutamyl transpeptidase (GGT). Moreover, the signaling pathway of EPM was analyzed by focal adhesion kinase (FAK), extracellular regulated kinase 1/2 (ERK1/2), and RhoA Western blot. Also, a dominant negative (DN) RhoA-WB-F344 cell line (WBRhoA-DN) was constructed. We found that the levels of phosphorylation (p) of FAK and ERK1/2 were up-regulated by EPM. Most importantly, we also showed that RhoA is necessary for EPM-induced activation of FAK and ERK1/2 and bile duct formation. In addition, a dual luciferase-reporter assay and CHIP assay was performed to reveal that EPM regulates GGT IV and GGT V expression differentially, possibly mediated by C/EBPb. Taken together, these data demonstrated that EPM regulates bile duct formation of WB-F344 cells through effects on RhoA and C/EBPb, implicating a dual aspect of this morphoregulator in bile duct epithelial morphogenesis. J. Cell. Physiol. 226: 2807-2816, 2011. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:2807 / 2816
页数:10
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