Sikora E, Grzelakowska-Sztabert B
Acta Biochim Pol. 1983;30(2):193-201.
The effects of quinazoline antifolate CB 3703 on folate metabolism in mouse L-cells were examined by measuring the amount of 14C label in folate derivatives and its distribution in separated folylmono- and polyglutamates in the cells grown in the presence of radioactive folate and quinazoline. The total radioactivity of folyl derivatives in the quinazoline-treated cells did not exceed 15% of the radioactivity extracted from the control cells, in spite of the fact that quinazoline CB 3703 did not interfere with the uptake of folate into L-cells. Analysis of folylmono- and polyglutamate derivatives, either incubated or not incubated with gamma-glutamylcarboxypeptidase, by chromatography on Sephadex G-25, G-15 or DEAE-cellulose revealed that in the quinazoline-treated cells practically all radioactivity was found in the position of unmetabolized folate. It seems probable, therefore, that quinazoline CB 3703 impairs in L-cells folate reduction and conversion to its coenzymatic forms and their subsequent polyglutamation. These facts seem to be responsible for a decrease in retention of folate derivatives in the quinazoline CB 3703-treated cells.
通过测量在放射性叶酸和喹唑啉存在下生长的细胞中叶酸衍生物的14C标记量及其在分离的单谷氨酸和多谷氨酸叶酸中的分布,研究了喹唑啉抗叶酸剂CB 3703对小鼠L细胞叶酸代谢的影响。尽管喹唑啉CB 3703不干扰叶酸进入L细胞,但喹唑啉处理的细胞中叶酸衍生物的总放射性不超过从对照细胞中提取的放射性的15%。通过在Sephadex G - 25、G - 15或DEAE - 纤维素上进行色谱分析,对与γ-谷氨酰羧肽酶一起孵育或未孵育的单谷氨酸和多谷氨酸叶酸衍生物进行分析,结果显示,在喹唑啉处理的细胞中,几乎所有的放射性都出现在未代谢叶酸的位置。因此,喹唑啉CB 3703似乎会损害L细胞中叶酸的还原及其向辅酶形式的转化以及随后的多谷氨酸化。这些事实似乎是喹唑啉CB 3703处理的细胞中叶酸衍生物保留减少的原因。