[Epithelial-mesenchymal transition of biliary epithelial cells in advanced liver fibrosis].

F Schulze, K Schardt, I Wedemeyer, E Konze, K Wendland, O Dirsch, U Töx, H P Dienes, M Odenthal
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引用次数: 0

Abstract

Unlabelled: The conversion of epithelial cells in a mesenchymal cell type is called "epithelial-mesenchymal-transition" (EMT). This process is defined by a loss of epithelial specific characteristics such as cell adhesion, polarity and a reorganization of cytoskeletal proteins. EMT has been shown to be involved in progression of cancer and in obstructive renal fibrosis. In this study we analyzed liver tissues in a bile-duct ligation model of rats and human liver biopsies with cholestatic fibrosis and chronic hepatitis c infection to determine if biliary epithelial cells undergo phenotypical and functional changes during chronic injury.

Methods: Liver tissue of rats and human patients was examined by immunohistochemistry using antibodies against epithelial and mesenchymal specific targets as well as molecules of potentially activated signaling pathways. To study contribution of biliary epithelial cells in extracellular matrix production we performed laser microdissection combined with real-time PCR.

Results: Bile duct ligation in rats induced a prominent biliary epithelial proliferation and a pronounced expression of vimentin was observed in biliary epithelial cells, whereas no vimentin expression was detectable in bile duct cells of sham operated rats. In human liver biopsies from patients with cholestatic fibrosis and chronic hepatitis c infection a prominent biliary expression of vimentin could be shown. Despite this, epithelial marker proteins were still detectable. Further, we observed collagen I mRNA expression in laser microdissected bile ducts.

Conclusion: Biliary epithelial cells show cytoskeletal rearrangements during chronic liver injury towards a mesenchymal phenotype. The detection of collagen I mRNA in bile duct cells suggests that they might participate in extracellular matrix production.

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[晚期肝纤维化患者胆道上皮细胞上皮-间质转化]。
未标记:上皮细胞向间充质细胞类型的转化称为“上皮-间充质-转化”(epithelial-mesenchymal-transition, EMT)。这一过程的定义是上皮特异性特征的丧失,如细胞粘附、极性和细胞骨架蛋白的重组。EMT已被证明与癌症进展和阻塞性肾纤维化有关。在这项研究中,我们分析了大鼠胆管结扎模型中的肝脏组织,以及胆汁淤积性纤维化和慢性丙型肝炎感染的人类肝脏活检,以确定慢性损伤期间胆道上皮细胞是否发生表型和功能变化。方法:采用免疫组化方法检测大鼠和人肝组织,使用针对上皮和间充质特异性靶点的抗体以及潜在激活的信号通路分子。为了研究胆道上皮细胞在细胞外基质生成中的作用,我们采用激光显微解剖结合实时荧光定量PCR技术。结果:大鼠胆管结扎诱导胆道上皮细胞显著增殖,胆道上皮细胞明显表达vimentin,而假手术大鼠胆道细胞未检测到vimentin表达。在胆汁淤积性纤维化和慢性丙型肝炎感染患者的肝脏活检中,可以显示出明显的胆道表达vimentin。尽管如此,上皮标记蛋白仍可检测到。此外,我们观察了激光显微解剖胆管中胶原I mRNA的表达。结论:胆道上皮细胞在慢性肝损伤过程中呈现细胞骨架重排,向间充质表型转变。胆管细胞中胶原I mRNA的检测提示它们可能参与细胞外基质的产生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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[The complement system]. [Familial hemophagocytic lymphohistiocytosis]. [Drug-induced liver injury]. Molecular pathology of lung cancer [Chronic myeloproliferative diseases].
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