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弗氏红白血病细胞体外分化过程中的地塞米松敏感和不敏感反应。

Dexamethasone-sensitive and -insensitive responses during in vitro differentiation of Friend erythroleukemia cells.

作者信息

Tsiftsoglou A S, Wong W, Housman D E

出版信息

Biochim Biophys Acta. 1983 Sep 13;759(3):160-9. doi: 10.1016/0304-4165(83)90308-2.

Abstract

We have investigated the mechanism(s) by which dexamethasone inhibit DMSO-induced Friend erythroleukemia cell differentiation in vitro. In particular, we examined the effects of dexamethasone on (a) the early events of differentiation such as cell volume alterations and 'memory response' and (b) the onset of biochemical events associated with terminal erythroid cell differentiation. By analysing kinetics of commitment of Friend cells to terminal erythroid differentiation on a clonal basis, we have observed that dexamethasone inhibited the completion of the latent period (time elapsed prior to commitment) and impaired "memory" (ability to inducer-treated cells to continue differentiation after a discontinuous exposure to inducer). Treatment of Friend cells with dexamethasone did not prevent the occurrence of DMSO-induced alterations in cell volume. However, dexamethasone treatment prevented a series of biochemical events associated with terminal Friend cell differentiation. These include the decrease in the rate of both cytoplasmic and nuclear RNA synthesis as well as the induction of cytidine deaminase activity and hemoglobin synthesis. These data indicate that the dexamethasone-sensitive process(es) operate during the early stages of Friend cell differentiation and that they are responsible for the inhibition of terminal erythroid maturation. These dexamethasone-sensitive processes, however, appear to be different from those regulating cell volume alterations during the early steps of DMSO-induced Friend cell differentiation.

摘要

我们研究了地塞米松在体外抑制二甲基亚砜(DMSO)诱导的弗氏红白血病细胞分化的机制。具体而言,我们检测了地塞米松对以下方面的影响:(a)分化的早期事件,如细胞体积变化和“记忆反应”;(b)与终末红细胞分化相关的生化事件的起始。通过在克隆水平分析弗氏细胞向终末红细胞分化的动力学过程,我们观察到地塞米松抑制了潜伏期(承诺分化前经过的时间)的完成,并损害了“记忆”(诱导剂处理的细胞在间断暴露于诱导剂后继续分化的能力)。用地塞米松处理弗氏细胞并不能阻止DMSO诱导的细胞体积变化的发生。然而,地塞米松处理阻止了一系列与弗氏细胞终末分化相关的生化事件。这些事件包括细胞质和细胞核RNA合成速率的降低以及胞苷脱氨酶活性和血红蛋白合成的诱导。这些数据表明,地塞米松敏感的过程在弗氏细胞分化的早期阶段起作用,并且它们负责抑制终末红细胞成熟。然而,这些地塞米松敏感的过程似乎与在DMSO诱导的弗氏细胞分化早期调节细胞体积变化的过程不同。

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