朱元贵, 卓光生, 陈志哲, 陈晓春. 寡核苷酸的摄取与血液肿瘤细胞种类和增殖活性的关系J. 药学学报, 2003, 38(6): 401-404.
引用本文: 朱元贵, 卓光生, 陈志哲, 陈晓春. 寡核苷酸的摄取与血液肿瘤细胞种类和增殖活性的关系J. 药学学报, 2003, 38(6): 401-404.
ZHU Yuan-gui, ZHUO Guang-sheng, CHEN Zhi-zhe, CHEN Xiao-chun. Oligonucleotide uptake in hematological tumor cells is related to cellular species and proliferationJ. Acta Pharmaceutica Sinica, 2003, 38(6): 401-404.
Citation: ZHU Yuan-gui, ZHUO Guang-sheng, CHEN Zhi-zhe, CHEN Xiao-chun. Oligonucleotide uptake in hematological tumor cells is related to cellular species and proliferationJ. Acta Pharmaceutica Sinica, 2003, 38(6): 401-404.

寡核苷酸的摄取与血液肿瘤细胞种类和增殖活性的关系

Oligonucleotide uptake in hematological tumor cells is related to cellular species and proliferation

  • 摘要: 目的探讨血液肿瘤细胞摄取寡核苷酸与其种类和活性的关系。方法流式细胞仪测定细胞内的平均荧光强度。结果经过0.60 μmol·L-1 荧光素FITC标记的G3139作用4 h后,血液系统肿瘤患者外周血及骨髓单个核细胞对G3139的摄取能力明显高于正常人;不同来源的血液肿瘤细胞株摄取G3139的能力不同,单核细胞、B淋巴细胞和髓系粒细胞来源的白血病细胞的摄取能力明显高于T淋巴细胞来源的白血病细胞;经过全反式维甲酸作用的HL60细胞的增殖活性明显受到抑制,同时细胞摄取G3139的能力明显下降。结论血液肿瘤细胞具有摄取寡核苷酸的能力,这种摄取能力与其细胞种类和细胞增殖活性有关。

     

    Abstract: AimTo explore whether the oligonucleotide upkake in hematological tumor cells is related to cellular species and proliferation. MethodsIntracellular mean fluorescence intensity was measured by flow cytometry. ResultsAfter treatment with FITC-labeled G3139 at the concentration of 0.60 μmol·L-1 for 4 h, the G3139 uptake into peripheral blood mononuclear cell and bone marrow mononuclear cell in hematological tumor patients was significantly higher than that in normal control. There was different uptake of G3139 among the malligant hematological tumor cell strains, and the uptake in cells derived from monocyte, B lymphocyte and myeloid cell was much higher than that in cells derived from T lymphocyte. After treatment with all-trans retinoic acid (ATRA), HL60 cell proliferation was markedly inhibited and the uptake of G3139 decreased significantly. ConclusionHematological tumor cells were capable of taking up oligonucleotide, and the oligonucleotide uptake in hematological tumor cells is related to its cellular species and its activation.

     

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