Mager D, Bernstein A
J Cell Physiol. 1978 Mar;94(3):275-85. doi: 10.1002/jcp.1040940305.
Early transport changes occurring during Friend erythroleukemic cell differentiation are reported. A decrease in the rate of 86Rb transport was observed beginning approximately five hours after stimulation with 1.5% dimethylsulfoxide (DMSO), a potent inducer of Friend cell differentiation. By 12 to 14 hours after DMSO addition, the transport rate had stabilized at close to 60% of control level. This decrease in the rate of 86Rb transport preceded a previously reported decrease in cell volume. Other chemical inducers of Friend cells, such as hypoxanthine and ouabain, also caused early decreases in 86Rb influx. In contrast, xanthine, which does not induce Friend cell differentiation, also did not affect 86Rb influx. The transport of two amino acid analogues, alpha-aminoisobutyric acid and 2-aminobicyclo [2,2,1]-heptane-2-carboxylic acid, which differ in their mode of uptake, was also measured following induction by DMSO. The transport rates of both compounds decreased after a 12-hour exposure to DMSO. In contrast, the uptake of 3H-colchicine, a drug which diffuses passively across the cell membrane, was not significantly affected. Studies with several variant cell lines which do not synthesize hemoglobin in response to DMSO indicate that these non-inducible cells can be divided into two classes--those that demonstrate early changes in transport very similar to the changes observed in inducible cell lines and those which exhibit only small changes in transport. Results obtained using a revertant clone have helped to distinguish between those transport changes which are associated with the induction of hemoglobin synthesis and those which are not. In addition, these early transport changes may be useful in defining the stage in the differentiation process at which a particular variant line is blocked.
报道了弗氏红白血病细胞分化过程中早期发生的转运变化。在用1.5%二甲基亚砜(DMSO)刺激后约5小时开始观察到86Rb转运速率下降,DMSO是弗氏细胞分化的有效诱导剂。添加DMSO后12至14小时,转运速率稳定在对照水平的近60%。86Rb转运速率的这种下降先于先前报道的细胞体积减小。弗氏细胞的其他化学诱导剂,如次黄嘌呤和哇巴因,也导致86Rb流入早期减少。相比之下,不诱导弗氏细胞分化的黄嘌呤也不影响86Rb流入。在用DMSO诱导后,还测量了两种摄取方式不同的氨基酸类似物α-氨基异丁酸和2-氨基双环[2,2,1]庚烷-2-羧酸的转运。两种化合物在暴露于DMSO 12小时后转运速率均下降。相比之下,被动扩散穿过细胞膜的药物3H-秋水仙碱的摄取没有受到显著影响。对几种不响应DMSO合成血红蛋白的变异细胞系的研究表明,这些不可诱导细胞可分为两类——一类表现出与可诱导细胞系中观察到的转运早期变化非常相似的变化,另一类仅表现出转运的微小变化。使用回复克隆获得的结果有助于区分与血红蛋白合成诱导相关的转运变化和不相关的转运变化。此外,这些早期转运变化可能有助于确定特定变异系在分化过程中被阻断的阶段。