基础医学与临床 ›› 2013, Vol. 33 ›› Issue (5): 525-530.

• 研究论文 • 上一篇    下一篇

C6胶质瘤微环境中SIL-6R/GP130与MSCs瘤向转化的相关性

崔向荣,朱静,田杰,邓兵,李娅莎,白璐   

  1. 重庆医科大学附属儿童医院
  • 收稿日期:2012-05-08 修回日期:2012-08-27 出版日期:2013-05-05 发布日期:2013-05-29
  • 通讯作者: 朱静 E-mail:zhujing310@yahoo.com.cn
  • 基金资助:
    骨髓间充质干细胞瘤化中STAT3信号通路过度激活的作用机制与规避研究;骨髓间充质干细胞瘤化过程中的STAT3过度激活机制研究

Correlation of SIL-6R/GP130 and oncological transformation of MSCs in C6 glioma microenviroment

  • Received:2012-05-08 Revised:2012-08-27 Online:2013-05-05 Published:2013-05-29
  • Contact: Jing ZHU E-mail:zhujing310@yahoo.com.cn

摘要: 目的 通过骨髓间充质干细胞(MSCs)与C6胶质瘤细胞间接共培养,探讨在C6胶质瘤微环境中SIL-6R及GP130的过度激活和表达对MSCs向肿瘤方向转化的影响。 方法 用transwell 插入式培养皿结合6孔板构建间接共培养体系来模拟MSCs生长的微环境,用RT-QPCR检测细胞中GP130、STAT-3、CyclinD1和BCL-xl mRNA的表达;相差显微镜下观察细胞形态学;ELISA法检测上清液中SIL-6R的表达;免疫荧光法检测细胞膜上GP130的表达;Western blot检测细胞中STAT-3、CyclinD1、BCL-xl蛋白表达。 结果 实验组的MSCs呈现类似胶质瘤细胞样的形态;细胞中GP130、STAT-3、CyclinD1和BCL-xl mRNA的表达水平和上清液中SIL-6R的表达水平明显高于阴性对照组和空白组(P<0.05);实验组大部分细胞及阳性对照组的细胞膜上表达GP130蛋白,分别达到93%±5%和95%±5%,显著高于阴性对照组及空白组的0%(P<0.01),细胞中STAT-3、CyclinD1和BCL-xl的蛋白表达水平高于阴性对照组和空白组(P<0.05)。 结论 MSCs的恶性转变与SIL-6R/GP130的过度表达和激活存在一定的相关性,但其在MSCs瘤向转变中的作用及机制有待进一步研究。

关键词: 骨髓间充质干细胞, SIL-6R, GP130

Abstract: Objictive To determine the role of the over-expression of SIL-6R and GP130 on oncological differention of bone marrow mesenchymal stem cell(MSCs)by indirectly co-culturing MSCs and C6 glioma cells. Methods The combination of transwell insert culture dish and 6-well plates was used to build indirectly co-cultured system to simulate the microenvIronment of MSCs growth. GP130 in each group was measured by RT-QPCR and immunofluorescence, STAT-3, CyclinD1 and BCL-xl in each group was measured by RT-QPCR and Western blot, SIL-6R in each group was measured by ELISA, the cell morphological changes were observed by the phase contrast microscope. Results Experimental group cells showed tumor cell-like morphology. Compared with negative control group and blank group, GP130, STAT-3, CyclinD1 and BCL-xl mRNA and protein in experimental group were significantly increased (P<0.05), and there were no significant differences between experimental group and positive control group. The expression rate of GP130 reached 93%±5% in experimental group, while in both negative control and blank group was 0%(P

Key words: bone marrow mesenchymal stem cells, SIL-6R, GP130

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