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细胞内腐胺和亚精胺缺乏会导致天然多胺和甲基乙二醛双(脒腙)的摄取增加。

Intracellular putrescine and spermidine deprivation induces increased uptake of the natural polyamines and methylglyoxal bis(guanylhydrazone).

作者信息

Alhonen-Hongisto L, Seppänen P, Jänne J

出版信息

Biochem J. 1980 Dec 15;192(3):941-5. doi: 10.1042/bj1920941.

Abstract

Inhibition of polyamine synthesis by alpha-difluoromethylornithine in cultured Ehrlich ascites-carcinoma cells rapidly enhanced the uptake of exogenous putrescine, spermidine and spermine from the culture medium. In tumour cells exposed to the drug for 2 days, the intracellular concentration of spermidine was decreased to less than 10% of that found in untreated cells. However, the strikingly stimulated transport system brought the concentration of spermidine to the control values in less than 2h after supplementation of the cells with micromolar concentrations of the polyamine. In the absence of polyamine deprivation, tumour cells did not accumulate extracellular polyamines to any appreciable extent. Ascites-tumour cells deprived of putrescine and spermidine likewise concentrated methylglyoxal bis(guanylhydrazone) [1,1'-[methylethanedylidine)dinitrilo]diguanidine] at a greatly enhanced rate. A previous "priming of tumour cells with difluoromethylornithine followed by an exposure of the cells to methylglyoxal bis(guanylhydrazone) resulted in a marked and rapid anti-proliferative effect.

摘要

α-二氟甲基鸟氨酸对培养的艾氏腹水癌细胞多胺合成的抑制作用迅速增强了细胞从培养基中外源摄取腐胺、亚精胺和精胺的能力。在接触该药物2天的肿瘤细胞中,亚精胺的细胞内浓度降至未处理细胞中该浓度的10%以下。然而,在向细胞补充微摩尔浓度的多胺后不到2小时,受到显著刺激的转运系统就使亚精胺浓度恢复到对照值。在不存在多胺剥夺的情况下,肿瘤细胞不会在任何可观程度上积累细胞外多胺。缺乏腐胺和亚精胺的腹水肿瘤细胞同样以大大提高的速率浓聚甲基乙二醛双(脒腙)[1,1'-[甲基乙二烷基]二亚氨基]二胍。先前用二氟甲基鸟氨酸对肿瘤细胞进行“预处理”,然后使细胞接触甲基乙二醛双(脒腙),会产生显著且迅速的抗增殖作用。

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