Leppä S, Härkönen P, Jalkanen M
Department of Medical Biochemistry, University of Turku, Finland.
Cell Regul. 1991 Jan;2(1):1-11. doi: 10.1091/mbc.2.1.1.
Cell-matrix interactions play an important role in the maintenance of cell shape, supposed to be mediated by the anchorage of cellular cytoskeleton to extracellular matrix via matrix receptors. In this work the expression of one of the known matrix receptors, syndecan, was studied during the hormone-induced change in the phenotype of Shionogi 115 (S115) mouse mammary tumor cells. In the presence of testosterone, when S115 cells express fibroblastic phenotype, they increased their growth rate and became gradually anchorage independent. These cells, however, revealed strong RGDS-dependent binding to fibronectin (FN) but not binding to the heparin-binding domain of FN. Instead, S115 cells growth without testosterone showed epithelial morphology and binding to the heparin-binding domain of FN, suggesting an alteration of syndecan expression in hormone-treated S115 cells. As quantitated by radioimmunoassay and by Western blot, the amounts of both matrix-binding ectodomain of syndecan and syndecan mRNA (2.6 kb) declined in hormone-treated S115 cells. The addition of antiandrogen cyproterone acetate to culture medium opposed the effect of testosterone on syndecan mRNA. We thus propose that the inactivation of syndecan gene and the consequent suppression of syndecan expression is related to the altered adhesion properties, the disappearance of epithelial phenotype, and, on the other hand, to the appearance of transformed-like phenotype in hormone-treated S115 cells.
细胞与基质的相互作用在维持细胞形态方面起着重要作用,据推测这种作用是通过细胞骨架经基质受体锚定到细胞外基质来介导的。在这项研究中,我们研究了已知的基质受体之一syndecan在激素诱导下的Shionogi 115(S115)小鼠乳腺肿瘤细胞表型变化过程中的表达情况。在睾酮存在的情况下,当S115细胞表达成纤维细胞表型时,它们的生长速率增加并逐渐变得不依赖贴壁生长。然而,这些细胞显示出对纤连蛋白(FN)有强烈的RGDS依赖性结合,但不与FN的肝素结合结构域结合。相反,未添加睾酮培养的S115细胞呈现上皮形态并与FN的肝素结合结构域结合,这表明激素处理后的S115细胞中syndecan的表达发生了改变。通过放射免疫测定和蛋白质印迹法进行定量分析,发现激素处理后的S115细胞中syndecan的基质结合胞外结构域和syndecan mRNA(2.6 kb)的量均下降。向培养基中添加抗雄激素醋酸环丙孕酮可对抗睾酮对syndecan mRNA的影响。因此,我们认为syndecan基因的失活以及随之而来的syndecan表达的抑制与激素处理后的S115细胞黏附特性的改变、上皮表型的消失以及另一方面转化样表型的出现有关。