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粒细胞-巨噬细胞集落刺激因子对人U-937细胞摄取、磷酸化及核苷酸保留3'-叠氮-3'-脱氧胸苷的影响。

Effects of granulocyte-macrophage colony-stimulating factor on 3'-azido-3'-deoxythymidine uptake, phosphorylation and nucleotide retention in human U-937 cells.

作者信息

Dhawan R K, Kharbanda S, Nakamura M, Ohno T, Kufe D

机构信息

Laboratory of Clinical Pharmacology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115.

出版信息

Biochem Pharmacol. 1990 Dec 15;40(12):2695-700. doi: 10.1016/0006-2952(90)90589-d.

Abstract

Previous studies have demonstrated that granulocyte-macrophage colony-stimulating factor (GM-CSF) both increases and decreases levels of 3'-azido-3'-deoxythymidine (AZT) nucleotides in certain human myeloid cells. The present studies have examined the effects of GM-CSF on AZT metabolism in U-937 cells. The results demonstrate that GM-CSF stimulated AZT nucleotide formation in these cells. This stimulation was detectable during concurrent exposure to GM-CSF and AZT or as a result of pretreatment with GM-CSF. The GM-CSF-induced enhancement in AZT nucleotide formation was associated with a 4-fold increase in AZT uptake. The finding that uptake of AZT into U-937 cells was only partially sensitive to 6-[(4-nitrobenzyl)thio]-9-beta-D-ribofuranosylpurine (NBMPR) suggested a process primarily involving nonfacilitated diffusion. The results also demonstrate that treatment of U-937 cells with GM-CSF was associated with nearly a 2-fold increase in thymidine kinase activity. Moreover, the findings indicate that retention of AZT-MP and AZP-TP was prolonged significantly (P less than 0.05 and P less than 0.01 respectively) in association with GM-CSF treatment. Taken together, these results suggest that GM-CSF enhances the formation of AZT nucleotides by increasing AZT uptake and phosphorylation, as well as increasing retention of phosphorylated derivatives.

摘要

先前的研究表明,粒细胞巨噬细胞集落刺激因子(GM-CSF)在某些人类髓样细胞中既能增加也能降低3'-叠氮-3'-脱氧胸苷(AZT)核苷酸的水平。本研究检测了GM-CSF对U-937细胞中AZT代谢的影响。结果表明,GM-CSF刺激了这些细胞中AZT核苷酸的形成。在同时暴露于GM-CSF和AZT期间或GM-CSF预处理后均可检测到这种刺激作用。GM-CSF诱导的AZT核苷酸形成增强与AZT摄取增加4倍有关。AZT进入U-937细胞的摄取仅对6-[(4-硝基苄基)硫代]-9-β-D-呋喃核糖基嘌呤(NBMPR)部分敏感,这一发现提示该过程主要涉及非易化扩散。结果还表明,用GM-CSF处理U-937细胞与胸苷激酶活性增加近2倍有关。此外,研究结果表明,与GM-CSF处理相关,AZT-MP和AZP-TP的保留时间显著延长(分别为P<0.05和P<0.01)。综上所述,这些结果表明,GM-CSF通过增加AZT摄取和磷酸化以及增加磷酸化衍生物的保留来增强AZT核苷酸的形成。

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