Shimizu E, Takahashi Y, Shinohara A, Yamamoto Y, Yoshida S, Yamamoto A, Sone S, Takaue Y, Ogura T
3rd Department of Internal Medicine, Tokushima University School of Medicine, Japan.
J Cancer Res Clin Oncol. 1996;122(8):445-52. doi: 10.1007/BF01187155.
The biological effects of c-kit ligand (stem-cell factor: SCF) on an immortalized human megakaryocytic cell line (CMK) was evaluated using methods including the 3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay, surface marker analysis, DNA cell-cycle analysis and immunoblotting. SCF stimulated the growth of CMK cells. Incubation with SCF resulted in increased expression of IIb/IIIa platelet-related glycoprotein (gpIIb, IIIa), indicating enhanced differentiation of CMK cells. Treatment of CMK cells with SCF resulted in a decrease in the subpopulation in the G1 phase, with a reciprocal increase in those in the S phase and the G2 + M phase. Moreover, SCF significantly increased cellular expression of cyclin A, a regulatory subunit of cyclin-dependent protein kinase (CDK), and the ratio of phosphorylated/dephosphorylated retinoblastoma gene product (RB protein). These results suggest that SCF stimulates the growth and differentiation of megakaryocytic cells possibly through mechanisms related to the activation of cell-cycle-dependent serine/threonine kinase and inactivation of the nuclear tumor-suppressor gene product.
使用包括3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)检测、表面标志物分析、DNA细胞周期分析和免疫印迹在内的方法,评估了c-kit配体(干细胞因子:SCF)对永生化人巨核细胞系(CMK)的生物学效应。SCF刺激了CMK细胞的生长。与SCF孵育导致血小板相关糖蛋白IIb/IIIa(gpIIb、IIIa)表达增加,表明CMK细胞的分化增强。用SCF处理CMK细胞导致G1期亚群减少,S期和G2+M期亚群相应增加。此外,SCF显著增加了细胞周期蛋白依赖性蛋白激酶(CDK)的调节亚基细胞周期蛋白A的细胞表达,以及视网膜母细胞瘤基因产物(RB蛋白)的磷酸化/去磷酸化比率。这些结果表明,SCF可能通过与细胞周期依赖性丝氨酸/苏氨酸激酶激活和核肿瘤抑制基因产物失活相关的机制刺激巨核细胞的生长和分化。