Byers T L, Pegg A E
Department of Physiology, Milton S. Hershey Medical Center, Pennsylvania State University College of Medicine, Hershey 17033.
J Cell Physiol. 1990 Jun;143(3):460-7. doi: 10.1002/jcp.1041430309.
Control Chinese hamster ovary (CHO) cells and mutant CHO cells lacking ornithine decarboxylase activity (CHODC-) were used to study the regulation of polyamine uptake. It was found that the transport system responsible for this uptake was regulated by intracellular polyamine levels and that this regulation was responsible for the maintenance of physiological intracellular levels under extreme conditions such as polyamine deprivation or exposure to exogenous polyamines. Polyamine transport activity was enhanced by decreases in polyamine content produced either by inhibition of ornithine decarboxylase with alpha-difluoromethylornithine in CHO cells or via polyamine starvation of CHODC- cells. The provision of exogenous polyamines resulted in rapid and large increases in intracellular polyamine content followed by decreased polyamine transport activity. Soon after this decrease in uptake activity, intracellular polyamine levels then fell to near control values. Cells grown in the presence of exogenous polyamines maintained intracellular polyamine levels at values similar to those of control cells. Protein synthesis was necessary for the increase in transport in response to polyamine depletion, but appeared to play no role in decreasing polyamine transport. Bis(ethyl) polyamine analogues mimicked polyamines in the regulation of polyamine transport but this process was relatively insensitive to regulation by methylglyoxal bis(guanylhydrazone), a spermidine analogue known to enter cells via this transport system and to accumulate to very high levels.
使用对照中国仓鼠卵巢(CHO)细胞和缺乏鸟氨酸脱羧酶活性的突变CHO细胞(CHODC-)来研究多胺摄取的调节。发现负责这种摄取的转运系统受细胞内多胺水平的调节,并且这种调节负责在诸如多胺剥夺或暴露于外源性多胺等极端条件下维持生理细胞内水平。通过用α-二氟甲基鸟氨酸抑制CHO细胞中的鸟氨酸脱羧酶或通过CHODC-细胞的多胺饥饿所产生的多胺含量降低,可增强多胺转运活性。提供外源性多胺导致细胞内多胺含量迅速大幅增加,随后多胺转运活性降低。摄取活性降低后不久,细胞内多胺水平随即降至接近对照值。在存在外源性多胺的情况下生长的细胞将细胞内多胺水平维持在与对照细胞相似的值。蛋白质合成对于响应多胺耗竭时转运增加是必需的,但似乎在降低多胺转运中不起作用。双(乙基)多胺类似物在多胺转运调节方面模拟多胺,但该过程对甲基乙二醛双(胍腙)的调节相对不敏感,甲基乙二醛双(胍腙)是一种已知通过该转运系统进入细胞并积累到非常高水平的亚精胺类似物。