Lacour F, Harel L, Friend C, Huynh T, Holland J G
Proc Natl Acad Sci U S A. 1980 May;77(5):2740-2. doi: 10.1073/pnas.77.5.2740.
The effect of the aminonucleoside of puromycin (AMS) on Friend erythroleukemia cells in culture was investigated, because purines and purine analogues are known to act as inducers of differentiation. After treatment with 20-30 micro M AMS for 4 days, the cultures contained between 80 and 90% benzidine-positive cells. Stimulation of hemoglobin synthesis was dose and time dependent. Inosine had no stimulatory activity; however, when it was added to the medium together with AMS, erythroid differentiation was almost completely inhibited. The inhibitory effect of inosine on this potent inducer was also dose and time dependent. No cytotoxicity was observed with either compound, alone or in combination. Inhibition of AMS stimulation of erythroid differentiation was also observed in the presence of inosine monophosphate and poly(inosinic acid). Hypoxanthine had a dual effect. At high concentrations (500 microgram/ml) it acted as an inducer, but when added at low concentrations (20 microgram/ml) together with AMS it inhibited differentiation. These findings suggest there is a link between purine biosynthesis and the event(s) required to trigger differentiation. Agonist-antagonist activity of closely related biological compounds has thus been revealed in the erythroleukemia cells.
由于已知嘌呤和嘌呤类似物可作为分化诱导剂,因此研究了嘌呤霉素氨基核苷(AMS)对培养的Friend红白血病细胞的影响。用20 - 30微摩尔/升的AMS处理4天后,培养物中含有80%至90%的联苯胺阳性细胞。血红蛋白合成的刺激呈剂量和时间依赖性。肌苷没有刺激活性;然而,当它与AMS一起添加到培养基中时,红系分化几乎完全受到抑制。肌苷对这种强效诱导剂的抑制作用也呈剂量和时间依赖性。单独或联合使用这两种化合物均未观察到细胞毒性。在肌苷一磷酸和聚肌苷酸存在的情况下,也观察到AMS对红系分化刺激的抑制作用。次黄嘌呤具有双重作用。在高浓度(500微克/毫升)时,它作为诱导剂起作用,但当与AMS一起以低浓度(20微克/毫升)添加时,它会抑制分化。这些发现表明嘌呤生物合成与触发分化所需的事件之间存在联系。因此,在红白血病细胞中揭示了密切相关生物化合物的激动剂 - 拮抗剂活性。