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EB1089对人原始巨核白血病细胞系的诱导分化作用

Effects of EB1089 on Differentiation of Human Megakaryoblastic Leukemia Cell Line
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摘要 EB1089是1,25-二羟维生素D3[1,25(OH)2D3]的新型类似物。以新近建立的一株人原始巨核白血病细胞系(HIMeg)为模型研究发现,在悬浮培养体系中,EB1089可以明显地抑制HIMeg细胞的增殖过程,且具有时间和剂量依赖性特点,其效应明显强于1,25(OH)2D3。克隆增殖实验表明,即使在极低浓度(10-10~10-13mol/L)时,EB1089也可明显抑制HIMeg细胞的克隆增殖。免疫荧光分析显示,对照组只有约2%的细胞表达糖蛋白Ⅱb/Ⅲa(GPⅡb/Ⅲa),但经EB1089或1,25(OH)2D3处理4d后分别有90%和50%的细胞表达GPⅡb/Ⅲa。实验结果表明,EB1089对HIMeg细胞具有比1,25(OH)2D3更强的抑制增殖和诱导分化作用。由于EB1089的钙磷代谢调节作用甚弱,因此具有潜在的临床应用价值。 Using a recently established human megakaryoblastic leukemia cell line,HIMeg,the proliferation and differentiation of megakaryocytic cells in the presence of EB1089,a novel 1,25-dihydroxyvitamin D3[1,25(OH)2D3] analogue,were investigated. In a liquid culture system,EB1089 could inhibit the proliferation of HIMeg cells in a dose-and time-dependent fashion,and the effect of EB1089 was found to be much more active than that of 1, 25(OH)2D3.In a methylcellulose culture system, EB1089 inhibited colony formation by HIMeg cells even at very low concentrations(10-10 to 10-13mo1/L).Immunofluorescence analysis showed that 2% of the HIMeg cells expressed glycoprotein Ⅱb/Ⅲa(GPⅡb/Ⅲa)antigen without vitamin D3 compounds, whereas 90% and 50% of the cells expressed GPⅡb/Ⅲa with the addition of EB1089 and 1,25(OH)2D3,respectivly. These observations suggest that, like 1,25(OH)2D3,EB1089 could play an important role in the proliferation and differentiation of cells of megakaryocytic lineage and might be of potentially therapeutical interest.
作者 宋亮年
出处 《第二军医大学学报》 CAS CSCD 北大核心 1994年第4期301-305,共5页 Academic Journal of Second Military Medical University
基金 国家自然科学基金
关键词 EB1089 诱导分化 白血病 巨核细胞 dihydroxyvitamin D_3 EB1089 differentiation leukemia megakaryocytic lineage
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参考文献3

  • 1宋亮年,Stem Cells,1993年,11卷,4期,312页
  • 2宋亮年,Biochem Pharmcol,1992年,43卷,10期,2292页
  • 3Cheng T,Sci Chin,1991年,34卷,4期,412页

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