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首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Effect of glycosylphosphatidylinositol specific phospholipase D gene expression levels on complement mediated killing of leukemic cells in patients with chronic myeloid leukemia.
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Effect of glycosylphosphatidylinositol specific phospholipase D gene expression levels on complement mediated killing of leukemic cells in patients with chronic myeloid leukemia.

机译:慢性髓样白血病患者中糖基磷脂酰肌醇特异性磷脂酶D基因表达水平对补体介导的白血病细胞杀伤的影响。

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BACKGROUND: To explore the disparity in glycosylphosphatidylinositol phospholipase D (GPI-PLD) expression levels between mononuclear cells of chronic myeloid leukemia (CML) and healthy controls, and clarify the certain relation of GPI-PLD expression levels to complement mediated killing of leukemic cells. METHODS: Competitive RT-PCR was used to detect quantitatively the GPI-PLD mRNA in mononuclear cells. GPI-anchored CD55 and CD59 were analyzed by flow cytometry and Western blotting. Complement-mediated lysis was assessed by staining method of trypan blue dye. RESULTS: The GPI-PLD activities and their mRNA copies in CML patients were significantly lower than those in healthy adults. At the tenth day after treatment with bone marrow transplantation (BMT), the GPI-PLD activities and copies of GPI-PLD mRNA almost recovered to the expression levels of healthy subjects. The expression of both CD55 and CD59 in CML patients were significantly higher than those in healthy subjects. After treatment with insulin(10(-7) mol/l) plus glucose (16.7 mmol/l) for 48 h, the cellular GPI-PLD activity and mRNA levels in K562 cells derived from the leukemic cells of a CML patient all increased about 3-fold. Simultaneously, the GPI-anchored CD55 and CD59 on cell surfaces were released into the culturing medium, and the killing rate of complement-mediated K562 cell lysis increased almost 3 times. CONCLUSION: The decreased GPI-PLD expression may reduce the release of GPI-anchored CD55 and CD59 in leukemia cells and finally decrease complement mediated killing of these cells in chronic phase of CML.
机译:背景:探讨慢性髓性白血病(CML)单个核细胞与健康对照之间糖基磷脂酰肌醇磷酸酶D(GPI-PLD)表达水平的差异,并阐明GPI-PLD表达水平与介导的白血病细胞杀伤的互补关系。方法:采用竞争性RT-PCR定量检测单核细胞中GPI-PLD mRNA。通过流式细胞术和蛋白质印迹分析了GPI锚定的CD55和CD59。通过台盼蓝染料的染色方法评估补体介导的裂解。结果:CML患者的GPI-PLD活性及其mRNA拷贝明显低于健康成年人。在骨髓移植(BMT)治疗后的第10天,GPI-PLD活性和GPI-PLD mRNA的拷贝几乎恢复到健康受试者的表达水平。 CML患者中CD55和CD59的表达均显着高于健康受试者。用胰岛素(10(-7)mol / l)加葡萄糖(16.7 mmol / l)处理48小时后,来自CML患者白血病细胞的K562细胞的细胞GPI-PLD活性和mRNA水平均升高了约3倍。同时,GPI锚定的细胞表面CD55和CD59被释放到培养基中,补体介导的K562细胞裂解的杀伤率提高了近3倍。结论:降低的GPI-PLD表达可能减少了白血病细胞在慢性粒细胞白血病中GPI锚定的CD55和CD59的释放,并最终减少了补体介导的这些细胞的杀伤。

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