IFNα对肿瘤细胞上TRAIL受体DR4和DR5表达的调节及意义
肿瘤,,IFNα;DR4;DR5;肿瘤,1材料与方法,2结果,3讨论,参考文献:
摘要:目的研究IFNα对肿瘤细胞Colo205 TRAIL功能受体DR4和DR5表达的调节作用,以及IFNα刺激与肿瘤细胞对rTRAIL诱导凋亡敏感性的影响。方法Colo205细胞以IFNα刺激0、24、48和72 h;采用RTPCR方法检测DR4和DR5 基因表达;用间接免疫荧光染色结合流式细胞技术检测细胞表面DR4和DR5分子表达;采用annexinV和碘化丙锭双染色试剂盒检测细胞凋亡。结果IFNα刺激后,DR4和DR5 的mRNA在细胞表面的表达均有增加,刺激48 h,膜型DR4和DR5表达达到高峰值(16.7%和29.8%);rTRAIL凋亡诱导效应在IFNα刺激48 h的Colo205细胞中最高。结论IFNα上调死亡受体DR4、DR5的表达可能是其促进rTRAIL 诱导肿瘤凋亡的重要机制。关键词:IFNα;DR4;DR5;肿瘤
The significance of IFNα to the expression of trail receptor DR4 and DR5 in tumor cells
LI Yan, CAO Yunxin, ZHANG Yun, HUANG Haiyan, JIN Baiquan
(Department of immunity, Fourth Military Medical University, Xi′an, Shanxi Province, 710032,China)
Abstract:ObjectiveStudying of regulating on IFNα to the expression of DR4 and DR5, and its affection to rTRAILinduced apoptosis in Colo205 tumor cells.MethodsColo205 cells were stimulated by IFNα for indicated time period (0,24,48 and 72 hours),the expression of DR4 and DR5 gene were determined by RTPCR assay. The expression of cell surfacebound DR4 and DR5 were determined by indirect fluorescence staining and flow cytometry analysis. An annexin V and PI staining kit were used to determined the apoptosis induced by rTRAIL. ResultsThe expression of mRNA and cell surfacebound DR4 andDR5 of Colo205 cells were up regulated by IFNα stimulation. The level surfacebound of DR4 andDR5 reached peak at 48 hours after IFNα treatment. The peak of apoptosis effect induced by rTRAIL also exerted in Colo205 cells stimulated by IFNα for 48 hours.ConclusionIFNα may accelerate the tumor cell apoptosis induced by rTRAIL by upregulating the expression of DR4 and DR5 of tumor cells. ......
您现在查看是摘要页,全文长 9928 字符。