Weidner K M, Behrens J, Vandekerckhove J, Birchmeier W
Institut für Zellbiologie (Tumorforschung), Universitätsklinikum, Essen, Federal Republic of Germany.
J Cell Biol. 1990 Nov;111(5 Pt 1):2097-108. doi: 10.1083/jcb.111.5.2097.
The generation of invasiveness in transformed cells represents an essential step of tumor progression. We have previously shown that MDCK epithelial cells, which are deprived of intracellular adhesion by the addition of anti-Arc-1/uvomorulin antibodies, become invasive for collagen gels and embryonal heart tissue (Behrens, J., M. M. Mareel, F. M. Van Roy, and W. Birchmeier. 1989. J. Cell Biol. 108: 2435-2447.). Here we examined whether invasiveness is also induced by scatter factor, which is known to dissociate epithelial cells (Stoker, M., E. Gherardi, M. Perryman, and J. Gray. 1987. Nature (Lond.). 327:239-242.). Scatter factor was purified to homogeneity from conditioned medium of human fibroblasts by heparin-Sepharose chromatography, followed by cation exchange chromatography, gel filtration, or preparative SDS gel electrophoresis. We found that scatter factor represents a 92,000 mol wt glycoprotein which, apparently, is converted by limited proteolysis into disulfide-linked 62,000 and 34/32,000 mol wt subunits. Reversed phase HPLC and sequence analysis of tryptic peptides confirmed the suggested molecular structure, and revealed further that scatter factor exhibits sequence similarities to hepatocyte growth factor and to plasminogen. Purified scatter factor in fact induces the invasiveness into collagen matrices of MDCK epithelial cells, and induces or promotes the invasiveness of a number of human carcinoma cell lines. Apparently, the effect on the human cells depends on their respective degree of differentiation, i.e., cell lines with a less pronounced epithelial phenotype were more susceptible to the factor. Scatter factor does not seem to influence synthesis, steady-state level, and phosphorylation of the cell adhesion molecule Arc-1/uvomorulin. Thus, scatter factor represents a clearly defined molecular species which induces, in vitro, the progression of epithelial cells to a more motile, i.e., invasive phenotype.
转化细胞侵袭性的产生是肿瘤进展的一个关键步骤。我们之前已经表明,通过添加抗Arc-1/桥粒芯糖蛋白抗体使细胞内粘附丧失的MDCK上皮细胞,对胶原凝胶和胚胎心脏组织具有侵袭性(Behrens, J., M. M. Mareel, F. M. Van Roy, and W. Birchmeier. 1989. J. Cell Biol. 108: 2435 - 2447.)。在此我们研究了已知能使上皮细胞解离的分散因子是否也能诱导侵袭性(Stoker, M., E. Gherardi, M. Perryman, and J. Gray. 1987. Nature (Lond.). 327:239 - 242.)。通过肝素 - 琼脂糖层析,随后进行阳离子交换层析、凝胶过滤或制备性SDS凝胶电泳,从人成纤维细胞的条件培养基中纯化得到均一的分散因子。我们发现分散因子是一种分子量为92,000的糖蛋白,显然,它通过有限的蛋白水解作用转化为二硫键连接的分子量为62,000和34/32,000的亚基。反相HPLC和胰蛋白酶肽段的序列分析证实了所推测的分子结构,并进一步揭示分散因子与肝细胞生长因子和纤溶酶原具有序列相似性。事实上,纯化的分散因子可诱导MDCK上皮细胞对胶原基质的侵袭性,并诱导或促进多种人癌细胞系的侵袭性。显然,对人细胞的作用取决于它们各自的分化程度,即上皮表型不太明显的细胞系对该因子更敏感。分散因子似乎不影响细胞粘附分子Arc-1/桥粒芯糖蛋白的合成、稳态水平和磷酸化。因此,分散因子是一种明确界定的分子物质,在体外可诱导上皮细胞向更具运动性即侵袭性表型的进展。