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Effect of arsenic trioxide on cytokine expression by acute promyelocytic leukemia cells

机译:三氧化二砷对急性早幼粒细胞白血病细胞因子表达的影响

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Objective To detect the expression of cytokines by acute promyelocytic leukemia (APL) cells before and after exposure to arsenic trioxide. Methods Diagnoses were performed according to the FAB cytological classification criteria and cytogenetic criteria. Bone marrow or blood samples from APL patients were collected in heparinized tubes, then primary APL cells were separated by traditional Ficoll-Hypaque density centrifugation and purified after adherence to plastic surfaces. IL-1_β, IL-6, IL-8, TNFα and G-CSF levels in the leukemia cell culture supernatants were detected by ELISA. At the same time, nitro blue tetrazolium (NBT) reduction test was used to detect the differentiation of APL cells. Results After 96 hours exposure to arsenic trioxide, 10-6 mol/L in vitro or 10 mg/d in vivo, APL cells showed a significant increase of IL-1_β ( P < 0. 05) and G-CSF ( P < 0. 05) production, and a significant decrease of IL-6 (P<0. 05) and IL-8 (P<0. 05). However, there was no obvious variation of TNFa when compared with APL cells without exposure to arsenic trioxide. On the other hand, the proliferation ratio of APL cells in vitro was statistically correlated to the IL-1_β secretion ratio or G-CSF secretion ratio. The cell number ratio in patients with detectable IL-1_β or G-CSF was higher than that without detectable IL-1_β or G-CSF. Conclusion IL-1_β and G-CSF secretion may play an important role in the proliferation of APL cells after exposure to arsenic trioxide.
机译:目的检测急性早幼粒细胞白血病(APL)细胞暴露于三氧化二砷前后的细胞因子表达。方法按照FAB细胞学分类标准和细胞遗传学标准进行诊断。将来自APL患者的骨髓或血液样本收集在肝素化试管中,然后通过传统的Ficoll-Hypaque密度离心分离原代APL细胞,并在粘附于塑料表面后进行纯化。通过ELISA检测白血病细胞培养上清液中的IL-1_β,IL-6,IL-8,TNFα和G-CSF水平。同时,用硝基蓝四氮唑(NBT)还原试验检测APL细胞的分化。结果96小时暴露于三氧化二砷,体外10-6 mol / L或体内10 mg / d后,APL细胞显示IL-1_β(P <0. 05)和G-CSF(P <0 ·05)产生,并且IL-6(P <0.05)和IL-8(P <0.05)显着降低。但是,与未暴露于三氧化二砷的APL细胞相比,TNFa没有明显变化。另一方面,APL细胞的体外增殖率与IL-1_β分泌率或G-CSF分泌率在统计学上相关。可检测到IL-1_β或G-CSF的患者的细胞数比高于未检测到IL-1_β或G-CSF的患者。结论IL-1_β和G-CSF的分泌可能在三氧化二砷暴露后对APL细胞的增殖起重要作用。

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