Müssig Eva, Steinberg Thorsten, Kohl Annette, Chamulitrat Walee, Komposch Gerda, Tomakidi Pascal
Department of Orthodontics and Dentofacial Orthopaedics, Dental School, University of Heidelberg, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany.
Cell Tissue Res. 2008 Apr;332(1):57-71. doi: 10.1007/s00441-007-0551-y. Epub 2008 Jan 10.
Ethanol treatment of immortalised human gingival keratinocytes (IHGK) yields in an epithelium-like (EPI) and fibroblast-like (FIB) phenotype. With respect to the stratified gingival epithelium, putative structural and molecular differences assigning cells to these phenotypes have not, to date, been analysed in a three-dimensional tissue/epithelial context. Therefore, we generated epithelial equivalents (EEs) in organotypic co-cultures of IHGK, EPI and FIB cells for 1 and 2 weeks and conducted protein and gene expression studies on the EEs for epithelial biomarkers including keratin K14, integrin subunits alpha6 and beta1, E-cadherin, and mesenchymal vimentin. As in the EEs of IHGK and EPI, indirect immunofluorescence revealed continuous expression of beta1 integrin in EEs of FIB cells. However, FIB cells exhibited a significant down-regulation in K14 and integrin alpha6 protein and a loss of E-cadherin at week 2, whereas vimentin was increased. FIB EEs were devoid of transcripts for E-cadherin at both time points, although transcription of the other genes remained constant in all phenotypes. Thus, the FIB phenotype exhibited a poor epithelial structure coinciding with disturbances in the expression of epithelial biomarkers and the persistence of mesenchymal vimentin. Transcription analysis revealed post-transcriptional regulation of vimentin in IHGK and EPI and of K14 and alpha6 in FIB cells. Our findings indicate that differences in the epithelial integrity and expression of molecules in EEs allow for the discrimination of EPI and FIB cells. This suggests that FIB cells share features of epithelial-mesenchymal transition and reflect a more progressive stage in epithelial cell transformation.
用乙醇处理永生化人牙龈角质形成细胞(IHGK)可产生上皮样(EPI)和成纤维细胞样(FIB)表型。关于分层的牙龈上皮,迄今为止,尚未在三维组织/上皮环境中分析将细胞分配到这些表型的假定结构和分子差异。因此,我们在IHGK、EPI和FIB细胞的器官型共培养物中培养上皮等效物(EEs)1周和2周,并对EEs进行蛋白质和基因表达研究,以检测包括角蛋白K14、整合素亚基α6和β1、E-钙黏蛋白和间充质波形蛋白在内的上皮生物标志物。与IHGK和EPI的EEs一样,间接免疫荧光显示FIB细胞的EEs中β1整合素持续表达。然而,FIB细胞在第2周时K14和整合素α6蛋白显著下调,E-钙黏蛋白丢失,而波形蛋白增加。FIB EEs在两个时间点均无E-钙黏蛋白转录本,尽管其他基因的转录在所有表型中均保持恒定。因此,FIB表型表现出上皮结构不良,同时伴有上皮生物标志物表达紊乱和间充质波形蛋白持续存在。转录分析显示,波形蛋白在IHGK和EPI中存在转录后调控,而K14和α在FIB细胞中存在转录后调控。我们的研究结果表明,EEs中上皮完整性和分子表达的差异有助于区分EPI和FIB细胞。这表明FIB细胞具有上皮-间质转化的特征,反映了上皮细胞转化的一个更进展阶段。