Mager D, Bernstein A
J Supramol Struct. 1978;8(4):431-8. doi: 10.1002/jss.400080405.
Treatment of Friend erythroleukemia cells with several different chemical agents causes an early decrease in the 86Rb+ influx mediated by Na+/K+ adenosine triphosphatase (ATPase). These agents, which induce Friend cells to differentiate, include dimethylsulfoxide (DMSO), ouabain, hypoxanthine, and actinomycin D. The magnitude of the early decrease in 86Rb+ influx correlates with the proportion of cells in cultures of inducible Friend cell clones which later go on to synthesize hemoglobin. Compounds which do not incude differentiation in these cells, such as xanthine, exogenous hematin, and erythropoietin, do not cause a change in 86Rb+ influx. A change in the intracellular K+ ion concentration does not occur during induction by DMSO because, although there is a decrease in K+ content per cell soon after induction, there is a parallel decrease in cell volume. These results and previous observations from this laboratory are discussed in terms of the posible involvement of the Na+/K+ ATPase in Friend cell differentiation.
用几种不同的化学试剂处理弗瑞德红白血病细胞会导致由钠钾腺苷三磷酸酶(ATP酶)介导的86Rb +流入量早期下降。这些诱导弗瑞德细胞分化的试剂包括二甲基亚砜(DMSO)、哇巴因、次黄嘌呤和放线菌素D。86Rb +流入量早期下降的幅度与可诱导的弗瑞德细胞克隆培养物中后来继续合成血红蛋白的细胞比例相关。在这些细胞中不诱导分化的化合物,如黄嘌呤、外源性血红素和促红细胞生成素,不会引起86Rb +流入量的变化。在DMSO诱导过程中,细胞内钾离子浓度没有变化,因为尽管诱导后不久每个细胞的钾含量下降,但细胞体积也同时下降。根据钠钾ATP酶可能参与弗瑞德细胞分化的情况,对这些结果以及本实验室以前的观察结果进行了讨论。