Mori M, Miyazaki K
Department of Surgery, Saga Medical School, Japan.
Cell Tissue Res. 2000 May;300(2):331-44. doi: 10.1007/s004410000205.
Although peptide growth factors play an important role in the morphogenesis of gallbladder, little is known about how they effect the morphogenesis of gallbladder epithelial cells. Rabbit gallbladder epithelial cells (RGEC) were isolated and cultured in monolayer or collagen gels. Epidermal growth factor (EGF), hepatocyte growth factor (HGF), epimorphin, transforming growth factor-beta 1 (TGF-beta 1), and fibroblast-conditioned medium (FCM) were added to the cultured cells to clarify the effects of these peptides and FCM on morphogenesis of RGEC. RGEC suspended in collagen gels form spherical cysts with morphologic polarity. EGF, HGF, epimorphin, and FCM promoted cyst maturation by accelerating the proliferation and aggregation of clear, polarized vesicles. In contrast, TGF-beta 1 markedly inhibited DNA synthesis in both monolayer and collagen gel cultures and promoted formation of branching structures in collagen gels. Furthermore, in the presence of EGF, TGF-beta 1 induced a drastic change in morphogenesis, with the formation of branching networks that showed cell-cell contact only at sites where branches touched. RGEC-forming multicellular cysts did not express vimentin but expressed significant amounts of cytokeratin and regained junctional complexes. In contrast, TGF-beta 1-treated cells strongly expressed vimentin along with branching structures and showed decreases in cytokeratin expression and junctional complexes. Thus, TGF-beta 1 induces a mesenchyme-like cell shape accompanied by cytoskeletal molecular changes, with loss of both epithelial polarization and junctional complexes. These results suggest that the morphogenetic program of RGEC is likely to be determined by the interaction of these peptides and the timing of their presence.
尽管肽生长因子在胆囊形态发生中起重要作用,但关于它们如何影响胆囊上皮细胞的形态发生却知之甚少。分离兔胆囊上皮细胞(RGEC)并在单层或胶原凝胶中培养。将表皮生长因子(EGF)、肝细胞生长因子(HGF)、表皮形态发生素、转化生长因子-β1(TGF-β1)和成纤维细胞条件培养基(FCM)添加到培养的细胞中,以阐明这些肽和FCM对RGEC形态发生的影响。悬浮在胶原凝胶中的RGEC形成具有形态极性的球形囊肿。EGF、HGF、表皮形态发生素和FCM通过加速透明极化小泡的增殖和聚集促进囊肿成熟。相反,TGF-β1在单层和胶原凝胶培养中均显著抑制DNA合成,并促进胶原凝胶中分支结构的形成。此外,在EGF存在的情况下,TGF-β1诱导形态发生的剧烈变化,形成仅在分支接触部位显示细胞间接触的分支网络。形成多细胞囊肿的RGEC不表达波形蛋白,但表达大量细胞角蛋白并重新获得连接复合体。相反,经TGF-β1处理的细胞与分支结构一起强烈表达波形蛋白,并显示细胞角蛋白表达和连接复合体减少。因此,TGF-β1诱导间充质样细胞形状并伴有细胞骨架分子变化,同时上皮极化和连接复合体丧失。这些结果表明,RGEC的形态发生程序可能由这些肽的相互作用及其存在的时间决定。