Duraj J, Chorváth B, Simkovic D
Neoplasma. 1979;26(6):647-53.
Cell surface and calf serum proteins were released in vitro from cultured virus-transformed, chemically transformed and normal rat embryo fibroblasts in 0.2 M urea containing serum-free culture medium. Fibronectin (LETS protein) was found in considerably higher amount in medium from normal rat embryo fibroblasts than in that from transformed cells. Major calf serum protein released from cultured normal and transformed rat cells corresponded by its electrophoretic mobility to calf serum albumin. No substantial differences in electrophoretic patterns of calf serum proteins released from normal and transformed cells into the medium were found. Time course of release of serum proteins from cell surface was measured quantitatively with the aid of radioiodinated Staphylococcus aureus protein A radioimmune assay. More than 50% of cell bound calf serum proteins remained on cell surface after 24 hours of incubation in serum-free medium.
在含0.2M尿素的无血清培养基中,从培养的病毒转化、化学转化及正常大鼠胚胎成纤维细胞中体外释放细胞表面蛋白和小牛血清蛋白。发现正常大鼠胚胎成纤维细胞培养基中的纤连蛋白(LETS蛋白)含量比转化细胞培养基中的高得多。从培养的正常和转化大鼠细胞中释放的主要小牛血清蛋白,其电泳迁移率与小牛血清白蛋白相对应。未发现正常细胞和转化细胞释放到培养基中的小牛血清蛋白电泳图谱有实质性差异。借助放射性碘化金黄色葡萄球菌蛋白A放射免疫测定法定量测量了血清蛋白从细胞表面的释放时间进程。在无血清培养基中孵育24小时后,超过50%与细胞结合的小牛血清蛋白仍留在细胞表面。