Kaneko T, Nomura S, Oishi M
Cancer Res. 1984 May;44(5):1756-60.
Cell fusion with two genetically marked Friend (murine erythroleukemia) cells has made it possible to characterize the very early events leading to erythroid differentiation, particularly the nature of reactions initiated by inducers such as dimethyl sulfoxide. We have found that brief exposure of Friend cells to dimethyl sulfoxide (as well as butyric acid or hexamethylene-bisacetamide) induces an early cellular activity required for erythroid differentiation which is detected only by fusion with ultraviolet-irradiated cells. The induction process of this activity consists of at least two distinct stages. In the first stage, the reaction proceeds without supply of metabolites from the medium and exhibits sensitivity to tumor promoters. The second stage is tightly coupled to cellular metabolic activity, notably protein synthesis. Under normal conditions, the induced activity is short-lived, suggesting turnover of the molecules responsible for this activity. There appears to be a signal produced following dimethyl sulfoxide pulse which acts as an inducer for this activity. The signal remains active for as long as 40 hr when protein synthesis is blocked.
将两个带有遗传标记的弗瑞德(小鼠红白血病)细胞进行细胞融合,使得表征导致红系分化的极早期事件成为可能,特别是由二甲基亚砜等诱导剂引发的反应的性质。我们发现,将弗瑞德细胞短暂暴露于二甲基亚砜(以及丁酸或六亚甲基双乙酰胺)会诱导红系分化所需的早期细胞活性,这种活性只有通过与紫外线照射的细胞融合才能检测到。这种活性的诱导过程至少包括两个不同的阶段。在第一阶段,反应在不供应培养基中代谢物的情况下进行,并且对肿瘤促进剂敏感。第二阶段与细胞代谢活性紧密相关,特别是蛋白质合成。在正常情况下,诱导的活性是短暂的,这表明负责这种活性的分子会周转。在二甲基亚砜脉冲后似乎产生了一种信号,该信号作为这种活性的诱导剂。当蛋白质合成被阻断时,该信号可保持活性长达40小时。