Rahman A F, Liao S K, Dent P B
In Vitro. 1977 Sep;13(9):580-5. doi: 10.1007/BF02627854.
We have established conditions for the study of membrane glycoprotein synthesis and turnover in cultured human malignant melanoma cell lines using the labeled precursor [3H]glucosamine. Uptake of label increased parallel with cell growth, reaching a steady state in resting cultures. Fifteen to 30% of incorporated label can be released from the cells by trypsin treatment depending on the conditions of exposure to the enzyme, and about 50% of the incorporated label is spontaneously shed from the cells within 96 hr of incubation. Labeling in exhausted medium gave a 5- to 8-fold increase in uptake which was inhibited by addition of glucose (2 mg per ml) into the culture medium. The percentage of trypsin-releasable material was identical in fresh and exhausted medium; however, the percentage shed was less in cells initially labeled in exhausted medium. These data provide background information for further studies on the antigenic composition of the glycoproteins of cultured melanoma cells.
我们已经建立了利用标记前体[3H]葡糖胺研究培养的人恶性黑色素瘤细胞系中膜糖蛋白合成及周转的条件。标记物的摄取与细胞生长平行增加,在静止培养物中达到稳态。根据酶暴露条件,15%至30%掺入的标记物可通过胰蛋白酶处理从细胞中释放出来,并且在孵育96小时内约50%掺入的标记物会从细胞中自发脱落。在耗尽培养基中进行标记时,摄取量增加了5至8倍,向培养基中添加葡萄糖(每毫升2毫克)可抑制这种增加。新鲜培养基和耗尽培养基中胰蛋白酶可释放物质的百分比相同;然而,最初在耗尽培养基中标记的细胞中脱落的百分比更低。这些数据为进一步研究培养的黑色素瘤细胞糖蛋白的抗原组成提供了背景信息。