Jian-Hua Tang, Xiao-Jie Zhang, Yi-Dan Wang, Wen-Kai Li, Wang-Jiao He, Cheng-Hong Wang, Gui-Yuan Li
Department of Biochemistry, Institute of Biological Science and Technology, Central South University, Xiangya Road 88, Mail box 54number, Changsha, Hunan 410078, PR China.
Clin Chim Acta. 2005 Sep;359(1-2):115-24. doi: 10.1016/j.cccn.2005.03.045.
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.
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.
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.
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.
探讨慢性髓性白血病(CML)单核细胞与健康对照者糖基磷脂酰肌醇磷脂酶D(GPI-PLD)表达水平的差异,并阐明GPI-PLD表达水平与补体介导的白血病细胞杀伤之间的特定关系。
采用竞争性逆转录聚合酶链反应(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免疫印迹法分析GPI锚定的CD55和CD59。采用台盼蓝染色法评估补体介导的细胞溶解。
CML患者的GPI-PLD活性及其mRNA拷贝数显著低于健康成年人。骨髓移植(BMT)治疗10天后,GPI-PLD活性和GPI-PLD mRNA拷贝数几乎恢复到健康受试者的表达水平。CML患者CD55和CD59的表达均显著高于健康受试者。用胰岛素(10⁻⁷mol/L)加葡萄糖(16.�mmol/L)处理48小时后,源自CML患者白血病细胞的K562细胞的细胞GPI-PLD活性和mRNA水平均增加了约3倍。同时,细胞表面GPI锚定的CD55和CD59释放到培养基中,补体介导的K562细胞溶解的杀伤率几乎增加了3倍。
GPI-PLD表达降低可能减少白血病细胞中GPI锚定的CD55和CD59的释放,最终降低CML慢性期补体介导的这些细胞的杀伤作用。