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重庆医科大学附属儿童医院中心实验室、儿童发育疾病研究教育部重点实验室,重庆,400014
纸质出版日期:2014,
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张春敏, 朱 静, 燕 莎, 等. 骨髓间充质干细胞在C6脑胶质瘤细胞微环境中瘤性转化的生物学分析[J]. 重庆医科大学学报, 2014,38(5):591-596.
Zhang Chunmin, Zhu Jing, Yan Sha, et al. Biological analysis of malignant transformation of bone marrow-derived mesenchymal stem cells in the microenvironment of C6 glioma cells[J]. Journal of Chongqing Medical University, 2014,38(5):591-596.
张春敏, 朱 静, 燕 莎, 等. 骨髓间充质干细胞在C6脑胶质瘤细胞微环境中瘤性转化的生物学分析[J]. 重庆医科大学学报, 2014,38(5):591-596. DOI:
Zhang Chunmin, Zhu Jing, Yan Sha, et al. Biological analysis of malignant transformation of bone marrow-derived mesenchymal stem cells in the microenvironment of C6 glioma cells[J]. Journal of Chongqing Medical University, 2014,38(5):591-596. DOI:
目的:探讨骨髓间充质干细胞(bone marrow-derived mesenchymal stem cells,BMSCs)在 C6 脑胶质瘤细胞微环境中是否发生了生物学特性的改变。方法:全骨髓贴壁筛选法分离培养 SD 大鼠 BMSCs,免疫荧光(immunofluorescence,IF)法检测BMSCs表面标志分子CD90+、CD105+、CD45-;活细胞荧光染料 CM-Dil标记 BMSCs(CM-Dil+BMSCs),流式细胞术(flow cytome-try,FCM)检测标记效率,台盼蓝染色法连续监测 BMSCs 死亡率;CM-Dil+BMSCs与C6脑胶质瘤细胞直接接触共培养为直接共培养组,BMSCs与 C6 脑胶质瘤细胞非接触共培养为间接共培养组,阳性对照组为C6脑胶质瘤细胞单独培养,阴性对照组为 BMSCs单独培养,培养 7 d 后,IF法检测各组酸性胶质纤维蛋白(glial fibrillary acidic protein,GFAP)、CD90、CD105表达情况;FCM分选实验组CM-dil+BMSCs 和 C6 脑胶质瘤细胞,实时荧光定量聚合酶链反应(real time quantitative polymerase chain re-action,RT-qPCR)检测各组GFAP、PTEN、Bcl-xl、CyclinD1、CD90、CD105基因的表达。结果:①培养至第3代的BMSCs 90%以上表达CD90、CD105且不表达CD45;②IF结果显示直接共培养组、间接共培养组BMSCs细胞表达GFAP水平较阴性对照组 BMSCs均增高。③RT-qPCR 结果显示直接共培养组、间接共培养组BMSCs 细胞GFAP、PTEN、Bcl-xl、CyclinD1基因表达水平较阴性对照组BMSCs明显增高(P<0.05),且直接共培养组与间接共培养组比较无明显差异(P >0.05);同时,直接共培养组、间接共培养组BMSCs的CD90、CD105基因表达水平较阴性对照组BMSCs显著降低(P<0.05)。结论:BMSCs 在C6脑胶质瘤细胞微环境中存在潜在瘤性转化的倾向。
Objective:To discuss the changes of the biological characteristics of bone marrow-derived mesenchymal stem cells(BMSCs) in the microenvironment of C6 glioma cells. Methods:Whole bone marrow adherent cultivation was used to isolate and culture SD rat BMSCs. Immunofluorescence(IF) was used to detect the surface makers of BMSCs(CD90+,CD105+,CD45-). BMSCs was labeled with a fluorescent dye CM-Dil(CM-Dil+BMSCs) and the labeling efficiency was examined with flow cytometry(FCM). The inhibitory rate of CM-Dil+BMSCs was continuously tested by trypan blue staining assay. In direct-co-culture group,CM-Dil+BMSCs was directly co-cultured with C6 glioma cells;in indirect-co-culture group,BMSCs was indirectly co-cultured with C6 glioma cells;in positive control group,C6 glioma cells was separately cultured and in negative control group,BMSCs was separately cultured. After 7 d,IF was applied to detect the expression of glial fibrillary acidic protein(GFAP) of each group. Gene expression of GFAP,PTEN,Bcl-xl,CyclinD1,CD90,CD105 of each group was detected by real time quantitative polymerase chain reaction(RT-qPCR). Results:(1)It was showed by IF that more than 90% of the third generation of BMSCs expressed CD90,CD105,but not CD45. (2)Expression of GFAP of BMSCs in direct-co-culture group and indirect-co-culture group was increased compared with that in negative control group,while the expression of CD90 and CD105 were decreased. Gene expression of GFAP,PTEN,Bcl-xl,CyclinD1 was significantly increased in direct-co-culture group and indirect-co-culture group compared with that in negative control group(P<0.05). There was no difference between direct-co-culture group and indirect-co-culture group(P >0.05). Gene expression of CD90,D105 was significantly decreased in direct-co-culture group and indirect-co-culture group compared with that in negative control group(P<0.05). Conclusion:BMSCs in the microenvironment of C6 glioma cells have the potential malignant transformation tendency.
骨髓间充质干细胞酸性胶质纤维蛋白C6脑胶质瘤细胞
bone marrow-derived mesenchymal stem cellsglial fibrillary acidic proteinC6 glioma cells
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