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调节Th1/Th2平衡对脑胶质瘤细胞增殖的影响

Influence of Adjustment of Balance of Th1/Th2 Type Cytokines on Proliferation of Glioma Cells

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【作者】 胡永生张庆林田志刚魏海明张建华李刚庞琦王成伟金澎孙汭

【Author】 Hu Yong-sheng  Zhang Qing-lin # Tian Zhi -gang  Wei Hai-ming  Zhang Jian-hua  Li Gang  Pang Qi Wang Cheng-wei Jin Peng Sun Rui  (Department of Neurosurgery,the Second Hospital of Shand

【机构】 山东大学第二医院神经外科山东大学第二医院神经外科 济南2

【摘要】 目的研究外源性细胞因子调节Th1/Th2平衡对脑胶质瘤细胞增殖的影响。方法分别将IFN-γ+IL-4单抗或IL-4+IFN-γ单抗与脑胶质瘤细胞共同孵育,半定量RT-PCR方法观察Th1/Th2类细胞因子基因表达的变化,并用MTT方法检测其对脑胶质瘤细胞生长情况的影响。结果脑胶质瘤细胞Th2类细胞因子的表达明显强于Th1类(P<0.01),IFN-γ+IL-4单抗可以增强IFN-γ的表达,抑制脑胶质瘤细胞的增殖并呈剂量依赖性关系(P<0.01);IL-4+IFN-γ单抗则使Th2类细胞因子的表达有所增强,促进脑胶质瘤细胞的增殖,也呈剂量依赖性关系(P<0.01)。结论外源性的细胞因子或细胞因子单抗可以调节Th1/Th2平衡,逆转Th2优势,影响脑胶质瘤细胞的生长。

【Abstract】 Objective To study the influence of adjustment of balance of Th1/Th2by external cytokines on proliferation of glioma cells.Methods The gene expressions of Th1/Th2type cytokines in C6,9L,U251and SHG44glioma cells were detected by semiquantitative reverse transcription polymerase chain reaction(RT-PCR).After the cells were induced with IFN-γ+IL-4McAb and IL-4+IFN-γMcAb respectively,we isolated the total RNA to proceed RT-PCR again.The evaluation of cell proliferation was pro ce eded by MTT assay method.Results There was obviously predominant expression of Th2type cytokines in glioma cell lines(P<0.01).The expression intensity of IFN-γwas improved in IF N-γ+IL-4McAb groups and Th2type cytokines were enhanced in IL-4+IFN-γMcAb groups.IFN-γand IL-4McAb could cause the switch from Th2to Th1,and could remarkably inhibit the proliferation of glioma cells in a dose-dependent way(P<0.01).On the other hand,IL-4and IFN-γMcAb could strengthen the switch of Th2,and might stimulate the glioma cell growth,also in a dose-dependent way(P<0.01).Conclusions There is a Th2preponderance in glioma cells.IFN-γand IL-4McAb could regulate the switch from Th2to Th0or Th1,and inhibit the proliferation of glioma cells.

【基金】 山东省“九五”科技攻关项目(鲁卫攻关08)资助
  • 【文献出处】 中国医学科学院学报 ,Acta Academiae Medicinae Sinicae , 编辑部邮箱 ,2001年06期
  • 【分类号】R739.4
  • 【被引频次】2
  • 【下载频次】75
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