首页 | 本学科首页   官方微博 | 高级检索  
     

2-甲氧基雌二醇诱导骨髓瘤细胞系CZ-1细胞分化作用初探
引用本文:高巍然,侯健. 2-甲氧基雌二醇诱导骨髓瘤细胞系CZ-1细胞分化作用初探[J]. 中华血液学杂志, 2005, 26(4): 197-199
作者姓名:高巍然  侯健
作者单位:200003,上海,第二军医大学长征医院血液科
摘    要:目的 观察2 甲氧基雌二醇对骨髓瘤细胞系CZ 1细胞诱导分化作用。方法 通过细胞形态观察,细胞表面标志分析和细胞分泌轻链蛋白水平的测定,观察2 甲氧基雌二醇对CZ 1细胞的诱导分化作用。结果 CZ 1细胞经0. 1~0. 5μmol/L2 甲氧基雌二醇作用48h后细胞形态向成熟阶段发展,表现为细胞胞核缩小,胞浆丰富,核浆比例下降,核仁减少或消失,核染色质变粗、变密。细胞表面标志CD49e阳性表达率由(12. 20±1. 57)%增加到( 24. 80±1. 26 )%,差异有统计学意义(P<0. 05); CZ 1细胞分泌轻链蛋白由(35. 97±2. 60)μg/ml升高到(79. 67±1. 88)μg/ml,差异有统计学意义(P<0. 05)。结论 较低浓度2 甲氧基雌二醇可诱导骨髓瘤细胞向成熟阶段分化。

关 键 词:雌二醇 骨髓瘤细胞 甲氧基 诱导 细胞分化 细胞形态 观察 细胞分泌 细胞表面标志 核仁
修稿时间:2004-04-26

Effect of 2-methoxyestradiol on cell differentiation of myeloma cell line CZ-1
GAO Wei-Ran,HOU Jian. Effect of 2-methoxyestradiol on cell differentiation of myeloma cell line CZ-1[J]. Chinese Journal of Hematology, 2005, 26(4): 197-199
Authors:GAO Wei-Ran  HOU Jian
Affiliation:Department of Hematology, Changzheng Hospital of Second Military Medical University, Shanghai 200003, China.
Abstract:OBJECTIVE: To investigate the differentiation induction effect of 2-methoxyestradiol (2ME2), an estrogen derivative on myeloma cell line CZ-1. METHODS: The changes of CZ-1 cells in morphology, expression of surface CD49e and quantity of light chain secretion in the supernatant were observed when treated with 0.1 approximately 0.5 micromol/L 2ME2 for 48 h. RESULTS: 2ME2 could induce differentiation of CZ-1 cells. The cells appeared decreased in size of nucleus, increased in cytoplasma, decreased in the ratio of nucleus to plasma, decreased in number or disappearance of nucleolus, and thickness and pyknosis of chromatin. The expression of CD49e was increased from (12.20 +/- 1.57)% to (24.80 +/- 1.26)% (P < 0.05). Light chain secretion in the supernatant was increased from (35.97 +/- 2.60) microg/ml to (79.67 +/- 1.88) microg/ml (P < 0.05). CONCLUSION: Low concentrations of 2ME2 could induce differentiation of myeloma cell line CZ-1.
Keywords:Estradiol  Cell differentiation  Cell line   myeloma
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号