首页 | 本学科首页   官方微博 | 高级检索  
检索        

外源性IL-4基因表达对K562细胞增殖及死亡的影响
引用本文:赵晓东,李成荣,杨锡强,李欣,黄贵清,蒋利萍.外源性IL-4基因表达对K562细胞增殖及死亡的影响[J].中国免疫学杂志,2000,16(4):208-210.
作者姓名:赵晓东  李成荣  杨锡强  李欣  黄贵清  蒋利萍
作者单位:重庆医科大学儿童医院,重庆,400014
基金项目:国家自然科学基金资助!(No.39470733)
摘    要:目的:观察外源性IL-4对K562增殖及死亡的影响。方法:用逆转录病毒载体将IL-4cDNA导入K562细胞,检测其增殖反应,用流式细胞依及DNA片段凝胶电泳检测细胞增殖周期及凋亡情况,用台盼蓝排除法计数死亡细胞。结果:高表达IL-4的K562细胞增殖反应明显低于表达株。亲代K562株;前者2过程中死亡细胞百分率明显升高且可被IL-4单克隆抗体阻断,但其自发凋亡细胞数及增殖周期均无改变。结论L:外

关 键 词:IL-4  基因治疗  白血病  细胞增殖  K562

The effect of exogenous IL-4 gene expression on cell death of K562 cells
ZHAO Xiao Dong,LI Cheng Rong,YANG Xi Qiang et al.Children's Hospital,Chongqing University of Medical Sciences,Chongqing.The effect of exogenous IL-4 gene expression on cell death of K562 cells[J].Chinese Journal of Immunology,2000,16(4):208-210.
Authors:ZHAO Xiao Dong  LI Cheng Rong  YANG Xi Qiang Children's Hospital  Chongqing University of Medical Sciences  Chongqing
Institution:ZHAO Xiao Dong,LI Cheng Rong,YANG Xi Qiang et al.Children's Hospital,Chongqing University of Medical Sciences,Chongqing 400014
Abstract:Objective: To observe the effect of exogenous IL 4 gene expression on cell death of K562 cells.Methods: IL 4 gene was transduced into K562 cell via retroviral vector mediated gene transfer method.Trypan blue stain,gel electrophoresis and flow cytometry were employed to determine cell death of K562 cell. Results:Proliferation of high IL 4 producing K562 clones was significantly lower than that of low IL 4 producing clones,parental K562 cells and K562 cells co cultured with recombinant IL 4.Cell death of high IL 4 producing K562 cells was enhanced dramatically and this effect could be blocked by IL 4 McAb,but its cell cycle no ever changed.There was no apoptosis determined.Conclusion: IL 4 expressed by IL 4 gene modified K562 cells could induce cell death of K562 cell by means of necrosis,which is benefitial for growth inhibition of leukemic cell.
Keywords:IL-4  Gene therapy  Leukemia
本文献已被 CNKI 维普 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