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两种慢性髓系白血病细胞株对干扰素-α的敏感性
作者姓名:Li XM  Chen HC  Liu XF  Wu YH  Cao YF
作者单位:中南大学湘雅医学院,分子生物学研究中心,湖南,长沙,410078
基金项目:中华医学基金( China Medical Board)(No.CMB 99-698);国家自然科学基金( No.39570805)
摘    要:背景和目的:临床研究表明干扰素-α(interferon-alpha,IFN-α)是造血系统恶性肿瘤和淋巴瘤的有效治疗剂之一。然而,IFN-α仅可使约70%~80%的慢性髓系白血病(chronic myeloid leukemia,CML)患者获得血液学缓解。不同的CML患者对IFN-α反应性不同的机制尚未阐明。本研究旨在比较两种CML细胞株KA-1/A3、K562对IFN-α的不同敏感性。方法:(1)采用MTT、半固体集落形成和台盼蓝染色液体培养细胞检测,不同浓度IFN-α(100、500、1000、5000和10000u/ml)对KT-1/A3及K562细胞生长的影响;(2)IFN-α(1000u/ml)诱导KT-1/A3、K562细胞48h后,采用流式细胞分析(flow cytometry,FCM)、荧光染色和DNA片段检测细胞凋亡;(3)加入IFN-α(1000u/m1)培养KT-1/A3、K562细胞48h后采用相对定量RT-PCR分析细胞bcr/abl基因表达水平。结果:(1)IFN-α呈剂量依赖性(从100u/ml到10000u/ml)抑制KT-1/A3细胞生长;(2)IFN-α(1000u/m1)诱导48h后使KT-1/A3细胞凋亡率从3.3%升到11.8%,并使KT-1/A3细胞中bcr/abl嵌合基因的表达水平降至对照组的66.7%;(3)IFN-α对K562细胞的生长、凋亡及bcr/abl嵌合基因表达无明显调节效应。结论:不同类型的CML细胞对IFN-α的反应性不同。

关 键 词:慢性髓系白血病  细胞株  干扰素-α  敏感性  基因表达  细胞凋亡
文章编号:1000-467X(2003)10-1047-06
修稿时间:2003年1月21日

Different sensitivity of two chronic myeloid leukemia cell lines to interferon-alpha
Li XM,Chen HC,Liu XF,Wu YH,Cao YF.Different sensitivity of two chronic myeloid leukemia cell lines to interferon-alpha[J].Chinese Journal of Cancer,2003,22(10):1047-1052.
Authors:Li Xin-Mei  Chen Han-Chun  Liu Xin-Fa  Wu Yan-Hui  Cao Yan-Fei
Institution:Molecular Biology Research Center, Xiangya Medical College, Central South University, Changsha, Hunan, 410078, PR China.
Abstract:BACKGROUND & OBJECTIVE: The clinical observation has shown that interferon-alpha(IFN-alpha) is one of the most effective therapeutic agents for the malignancies of hemopoietic system and lymphoma. However, IFN-alpha can only induce about 70-80% of the patients with chronic myeloid leukemia (CML) to get hematological remission. The mechanism by which various CML cases respond differently to IFN-alpha is still unclear. METHODS: (1)The effects of IFN-alpha in different concentrations (100, 500, 1,000, 5,000, and 10,000 U/ml) on growth of the two CML cell lines were detected by MTT assay,semisolid colony formation and trypan-blue staining for the cells in liquid culture. (2)The cell apoptosis was examined by flow cytometry(FCM),fluorescence microscopy and gel electrophoresis analysis for DNA fragmentation in 48 hours after IFN-alpha (1,000 U/ml) induction of both KT-1/A3 and K562 cells. (3)The expression levels of bcr/abl chimeric genes were analyzed by relative quantitative RT-PCR at 48 hours after cultivation of both KT-1/A3 and K562 cells with IFN-alpha in 1,000 U/ml. RESULTS: (1)The growth inhibition of KT-1/A3 cells was dose-dependent in IFN-alpha from the concentration of 100 U/ml to 10,000 U/ml. (2)Having been induced with IFN-alpha in 1000 U/ml for 48 hours, the apoptosis rate of KT-1/A3 cells raised from 3.29% to 11.8% and the expression level of bcr/abl chimeric gene in this cell line declined to 66.7% as compared with those of the control. (3)The growth and apoptosis rate as well as bcr/abl gene expression level of K562 cells were not significantly affected by IFN-alpha. CONCLUSION: Different populations of CML cells shows different sensitivity to IFN-alpha.
Keywords:Apoptosis  Chronic myeloid leukemia (CML)  Interferon  alpha  KT-1 /A3 cell line  K562 cell line
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