Plateroti M, Rubin D C, Duluc I, Singh R, Foltzer-Jourdainne C, Freund J N, Kedinger M
Institut National de la Santé et de la Recherche Médicale Unité 381, Strasbourg, France.
Am J Physiol. 1998 May;274(5):G945-54. doi: 10.1152/ajpgi.1998.274.5.G945.
The intestine is characterized by morphofunctional differences along the proximodistal axis. The aim of this study was to derive mesenchymal cell lines representative of the gut axis. We isolated and cloned rat intestinal subepithelial myofibroblasts raised from 8-day proximal jejunum, distal ileum, and proximal colon lamina propria. Two clonal cell lines from each level of the gut were characterized. They 1) express the specific markers vimentin, smooth muscle alpha-actin, and smooth muscle myosin heavy chain, revealed by immunofluorescence microscopy and 2) distinctly support endodermal cell growth in a coculture model, depending on their regional origin, and 3) the clones raised from the various proximodistal regions maintain the same pattern of morphogenetic and growth and/or differentiation factor gene expression as in vivo: hepatocyte growth and/or scatter factor and transforming growth factor-beta 1 mRNAs analyzed by RT-PCR were more abundant, in the colon and ileal clones and mucosal connective tissue, respectively. In addition, epimorphin mRNA studied by Northern blot was also the highest in one ileal clone, in which it was selectively upregulated by all-trans retinoic acid (RA) treatment. Epimorphin expression in isolated 8-day intestinal lamina propria was higher in the distal small intestine and proximal colon than in the proximal small intestine. In conclusion, we isolated and characterized homogeneous cell subtypes that can now be used to approach the molecular regulation of the epithelium-mesenchyme-dependent regional specificity along the gut.
肠道在近远轴上具有形态功能差异。本研究的目的是获得代表肠道轴的间充质细胞系。我们分离并克隆了从8日龄大鼠的近端空肠、远端回肠和近端结肠固有层培养的肠上皮下肌成纤维细胞。对肠道各部位的两个克隆细胞系进行了特性分析。它们1)表达波形蛋白、平滑肌α-肌动蛋白和平滑肌肌球蛋白重链等特异性标志物,免疫荧光显微镜检查可显示;2)在共培养模型中,根据其区域来源,能明显支持内胚层细胞生长;3)从不同近远区域培养的克隆细胞维持与体内相同的形态发生、生长和/或分化因子基因表达模式:通过逆转录聚合酶链反应分析的肝细胞生长和/或散射因子以及转化生长因子-β1信使核糖核酸,分别在结肠和回肠克隆以及黏膜结缔组织中更为丰富。此外,通过Northern印迹法研究的表皮形态发生素信使核糖核酸在一个回肠克隆中也最高,在该克隆中,全反式视黄酸(RA)处理可使其选择性上调。在分离的8日龄肠固有层中,表皮形态发生素的表达在远端小肠和近端结肠中高于近端小肠。总之,我们分离并鉴定了同质细胞亚型,这些亚型现在可用于研究沿肠道上皮-间充质依赖性区域特异性的分子调控。