首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Induction of differentiation of murine erythroleukemia cells by aminonucleoside of puromycin and inhibition of this induction by purines and purine derivatives.
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Induction of differentiation of murine erythroleukemia cells by aminonucleoside of puromycin and inhibition of this induction by purines and purine derivatives.

机译:嘌呤霉素的氨基核苷诱导鼠红细胞白血病细胞分化嘌呤和嘌呤衍生物抑制这种诱导。

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摘要

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.
机译:研究了嘌呤霉素(AMS)氨基核苷对培养中的Friend红白血病细胞的影响,因为已知嘌呤和嘌呤类似物可作为分化诱导剂。用20-30 micro M 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是剂量和时间依赖性的。肌苷没有刺激活性。但是,当将其与AMS一起添加到培养基中时,红系分化几乎被完全抑制。肌苷对该有效诱导剂的抑制作用也是剂量和时间依赖性的。单独或组合使用任何化合物均未观察到细胞毒性。在肌苷一磷酸和聚肌苷酸的存在下也观察到抑制AMS刺激红系分化。次黄嘌呤具有双重作用。在高浓度(500微克/毫升)时,它起诱导剂的作用,但在低浓度(20微克/毫升)中与AMS一起添加时,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。因此已经在红白血病细胞中揭示了密切相关的生物化合物的激动剂-拮抗剂活性。

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