PLATELET-LIKE PARTICLES RELEASED BY INHIBITION OF DNA SYNTHESIS IN THE HUMAN-MEGAKARYOBLASTIC LEUKEMIA CELL LINE, MEG-01s

M. Takeuchi, H. Kuno, M. Satoh, Touho Yoshida, M. Ogura, Kikuko Takeuchi
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引用次数: 5

Abstract

The human megakaryoblastic cell line, MEG-01s, released particles identified by a characteristic marginal microtubule bundle and by the localization of platelet-specific glycoprotein (GPIlb/Illa) in the plasma membrane, detected by an immunofluorescence method. The fluorescence image and size of these particles were similar to these features in human blood platelets. To analyze the regulation of particle release by MEG-01s, the effects of DNA synthesis inhibitors, tumor promoters, and protein kinase inhibitors on these cells were examined by an immunofluorescence method. The release of particles from MEG-Ols cells was enhanced by inhibitors of DNA synthesis : aphidicolin, 5-bromodeoxyuridine, 5-fluorodeoxyuridine, hydroxyurea, etoposide, and camptothecin. The particle release was specific to the MEG-01s cells, and did not occur in the myeloid leukemic cells, HL-60. These results suggest that the cessation of DNA synthesis may trigger terminal differentiation by synthesis of factors involving particle release by MEG-01s.
抑制人巨核母细胞白血病细胞系DNA合成释放的血小板样颗粒
人巨核母细胞系MEG-01s释放的颗粒通过特征边缘微管束和质膜中血小板特异性糖蛋白(GPIlb/Illa)的定位(通过免疫荧光法检测)来识别。这些颗粒的荧光图像和大小与人类血小板的特征相似。为了分析MEG-01s对颗粒释放的调控作用,采用免疫荧光法检测了DNA合成抑制剂、肿瘤启动子和蛋白激酶抑制剂对这些细胞的影响。DNA合成抑制剂:阿飞青霉素、5-溴脱氧尿苷、5-氟脱氧尿苷、羟基脲、依托opo苷和喜树碱增强了MEG-Ols细胞颗粒的释放。颗粒释放是MEG-01s细胞特异性的,而在髓性白血病细胞HL-60中没有发生。这些结果表明,DNA合成的停止可能通过合成与MEG-01s颗粒释放有关的因子来触发终端分化。
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