Kane M A, Elwood P C, Portillo R M, Antony A C, Najfeld V, Finley A, Waxman S, Kolhouse J F
Cancer Chemotherapy Foundation Laboratory, Mt. Sinai Medical Center, New York 10029.
J Clin Invest. 1988 May;81(5):1398-406. doi: 10.1172/JCI113469.
The influence of extracellular folate concentration on cellular levels of the folate transport protein and its soluble product was studied directly in cultured human nasopharyngeal carcinoma (KB) cells. As determined by radioimmunoassay, levels of the folate transport protein and the soluble folate-binding protein were 58 +/- 17 (mean +/- SD) and 5 +/- 2 pmol/mg cell protein, respectively, in KB cells maintained in standard medium (containing 2,300 nM folic acid). These levels significantly increased to 182 +/- 34 and 26 +/- 6 pmol/mg cell protein, respectively, in KB cells serially passaged in low folate medium (containing 2-10 nM 5-methyltetrahydrofolate). Increases in folate-binding protein levels occurred more rapidly in KB cells serially passaged in very low folate medium containing less than 2 nM folate and were prevented by the addition of 100 nM 5-methyltetrahydrofolate or 0.1-1 microM 5-formyltetrahydrofolate to this medium. When KB cells which had been passaged in low folate medium were passaged back into either standard medium or low folate medium supplemented with reduced folates, the levels of both folate-binding proteins fell linearly towards the levels in KB cells continuously maintained in standard medium. The folate transport protein was identified in and underwent similar changes in human and mouse mammary tumor cells. These studies indicate that the folate transport system is probably regulated by the extracellular folate concentration through changes in intracellular metabolite levels.
在培养的人鼻咽癌(KB)细胞中,直接研究了细胞外叶酸浓度对叶酸转运蛋白及其可溶性产物细胞水平的影响。通过放射免疫测定法测定,在标准培养基(含2300 nM叶酸)中培养的KB细胞中,叶酸转运蛋白和可溶性叶酸结合蛋白的水平分别为58±17(平均值±标准差)和5±2 pmol/mg细胞蛋白。在低叶酸培养基(含2 - 10 nM 5 - 甲基四氢叶酸)中连续传代的KB细胞中,这些水平分别显著增加至182±34和26±6 pmol/mg细胞蛋白。在含叶酸低于2 nM的极低叶酸培养基中连续传代的KB细胞中,叶酸结合蛋白水平增加更快,并且向该培养基中添加100 nM 5 - 甲基四氢叶酸或0.1 - 1 μM 5 - 甲酰四氢叶酸可阻止这种增加。当在低叶酸培养基中传代的KB细胞传回到标准培养基或添加还原型叶酸的低叶酸培养基中时,两种叶酸结合蛋白的水平均呈线性下降至在标准培养基中持续培养的KB细胞中的水平。在人和小鼠乳腺肿瘤细胞中鉴定出了叶酸转运蛋白,并且其也发生了类似的变化。这些研究表明,叶酸转运系统可能通过细胞内代谢物水平的变化受细胞外叶酸浓度的调节。