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集落刺激因子对全反式维甲酸诱导急性早幼粒细胞白血病细胞分化的影响。

Effects of colony-stimulating factors on the all-trans retinoic acid-induced differentiation of acute promyelocytic leukemic cells.

作者信息

Hsu H C, Tsai W H, Hsu M L, Ho C H, Wang S Y

机构信息

Department of Medicine, Veterans General Hospital-Taipei, Taiwan, R.O.C.

出版信息

Zhonghua Yi Xue Za Zhi (Taipei). 1996 Feb;57(2):93-9.

PMID:8634936
Abstract

BACKGROUND

NB4, a cell line derived from a patient with t(15;17) acute promyelocytic leukemia (APL) that undergoes granulocytic differentiation when treated with pharmacological doses of all-trans retinoic acid (ATRA), was used as a model for induction of differentiation. In this study, we examined the interaction of colony-stimulating factors (CSF) and ATRA in affecting the proliferation and differentiation of NB4 cells.

METHODS

Nitroblue tetrazolium (NBT) reduction was used as a functional marker of leukemia cell differentiation. The number of viable cells was counted by trypan blue exclusion test.

RESULTS

Proliferation of NB4 cells increased when exposed to 10(-9)M of ATRA, but reduced progressively when exposed to ATRA at the concentrations of 10(-8)M to 10(-6)M. After culture for 5 days, NBT-positive cell was not detectable in the control cultures with medium alone, but its percentage apparently increased to 84% at 10(-7)M ATRA. Granulocyte (G)-CSF per se had no effect on the granulocytic differentiation of NB4 cells, but it could enhance the NBT reduction when used in combination with various concentrations (10(-9)M -10(-6)M) of ATRA. Interleukin (IL)-3 or granulocyte-macrophage-CSF (GM-CSF) alone also had no effect on the NBT reduction in NB4 cells. However, when combined with ATRA, both caused a slight suppression of NBT reduction. No synergistic effect was noted between IL-3 and G-CSF on the ATRA-induced granulocytic differentiation.

CONCLUSIONS

G-CSF, but not IL-3 or GM-CSF, can enhance the differentiating activity of ATRA. Further investigations are necessary to evaluate its clinical use.

摘要

背景

NB4细胞系源自一名患有t(15;17)急性早幼粒细胞白血病(APL)的患者,当用药理剂量的全反式维甲酸(ATRA)处理时,该细胞系会发生粒细胞分化,被用作诱导分化的模型。在本研究中,我们检测了集落刺激因子(CSF)与ATRA在影响NB4细胞增殖和分化方面的相互作用。

方法

用硝基蓝四氮唑(NBT)还原作为白血病细胞分化的功能标志物。通过台盼蓝排斥试验计数活细胞数量。

结果

当暴露于10(-9)M的ATRA时,NB4细胞的增殖增加,但当暴露于浓度为10(-8)M至10(-6)M的ATRA时,增殖逐渐降低。培养5天后,仅含培养基的对照培养物中未检测到NBT阳性细胞,但在10(-7)M ATRA时其百分比明显增加至84%。粒细胞(G)-CSF本身对NB4细胞的粒细胞分化没有影响,但与各种浓度(10(-9)M - 10(-6)M)的ATRA联合使用时可增强NBT还原。单独的白细胞介素(IL)-3或粒细胞-巨噬细胞集落刺激因子(GM-CSF)对NB4细胞中的NBT还原也没有影响。然而,与ATRA联合使用时,两者均导致NBT还原略有抑制。IL-3和G-CSF在ATRA诱导的粒细胞分化方面未观察到协同作用。

结论

G-CSF可增强ATRA的分化活性,而IL-3或GM-CSF则不能。有必要进一步研究以评估其临床应用。

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