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粒细胞或粒细胞/巨噬细胞集落刺激因子与全反式维甲酸联合体外诱导急性早幼粒细胞白血病时,其增殖活性增强,成熟得到促进。

Potentiated maturation with a high proliferating activity of acute promyelocytic leukemia induced in vitro by granulocyte or granulocyte/macrophage colony-stimulating factors in combination with all-trans retinoic acid.

作者信息

Imaizumi M, Sato A, Koizumi Y, Inoue S, Suzuki H, Suwabe N, Yoshinari M, Ichinohasama R, Endo K, Sawai T

机构信息

Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Leukemia. 1994 Aug;8(8):1301-8.

PMID:7520101
Abstract

All-trans retinoic acid (ATRA) induces differentiation of acute promyelocytic leukemia (APL), but the effect of cytokines regulating myeloid differentiation on ATRA-induced APL cells is poorly understood. In this study, maturation and proliferation of fresh APL cells were examined when induced in vitro by granulocyte or granulocyte/macrophage colony-stimulating factors (G-CSF or GM-CSF) in combination with ATRA. APL cells showed a low proliferating activity when induced by ATRA alone. In contrast, cells induced by G-CSF or GM-CSF alone showed increased DNA syntheses, the levels of which were not significantly affected by the combination of ATRA with CSFs. Interestingly, G-CSF or GM-CSF potentiated the capability of ATRA-induced cells to reduce nitroblue tetrazolium (NBT), while G-CSF or GM-CSF alone induced no NBT reduction. Furthermore, in several patients examined, APL cells induced by ATRA with G-CSF showed an increased activity of chemotaxis and CD11a expression. These findings suggest that G-CSF or GM-CSF can potentiate differentiation of ATRA-induced APL cells while stimulating their proliferating activity as well, and that G-CSF, rather than GM-CSF, may be a useful adjunct to promote ATRA-induced differentiation of APL.

摘要

全反式维甲酸(ATRA)可诱导急性早幼粒细胞白血病(APL)细胞分化,但细胞因子对髓系分化的调节作用以及其对ATRA诱导的APL细胞的影响尚不清楚。在本研究中,检测了粒细胞集落刺激因子(G-CSF)或粒细胞/巨噬细胞集落刺激因子(GM-CSF)与ATRA联合体外诱导新鲜APL细胞时细胞的成熟和增殖情况。单独使用ATRA诱导时,APL细胞增殖活性较低。相比之下,单独使用G-CSF或GM-CSF诱导的细胞DNA合成增加,而ATRA与集落刺激因子联合使用对其水平无显著影响。有趣的是,G-CSF或GM-CSF增强了ATRA诱导细胞还原硝基蓝四氮唑(NBT)的能力,而单独使用G-CSF或GM-CSF则不能诱导NBT还原。此外,在检测的几名患者中,ATRA与G-CSF联合诱导的APL细胞趋化活性和CD11a表达增加。这些发现表明,G-CSF或GM-CSF可增强ATRA诱导的APL细胞分化,同时刺激其增殖活性,并且G-CSF而非GM-CSF可能是促进ATRA诱导APL细胞分化的有用辅助药物。

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