Yu Sheng-ping, Yang Xue-jun, Zhang Bin, Ming Hao-lang, Liu Bin, Liu Zhi-feng, Ren Bing-cheng, Chen Cong, Gao Wei
Department of Neurosurgery, Tianjin Medical University General Hospital & Laboratory of Neuro-oncology, Tianjin Neurological Institute, Tianjin 300052, China.
Zhonghua Wai Ke Za Zhi. 2012 May;50(5):452-6.
To dynamically observe how glioma stem cells promote the tumor formation and angiogenesis, and to study the correlation between the distribution of glioma stem cells and microvessels within different growth stages of subcutaneous tumor.
Stem cell medium culture and magnetic activated cell sorting were carried out to obtain CD133+ cells from C6 rat glioma cell line. Sprague Dawley (SD) rat ears model were established to observe glioma stem cells promoting blood vessel formation. Subcutaneous glioma model of C6 and immunohistochemical staining of hypoxia inducible factor-1α (HIF-1α) and CD133 were used to investigate the relationship between distribution of glioma stem cells and microvessels. Expressions of CD133 protein in each stage of the subcutaneous tumor were detected by Western blot.
Isolation and identification of glioma stem cells deprived from C6 glioma cell line successfully, the establishment of ears model showed real-time dynamic observation of CD133+ cells involved in angiogenesis and tumor formation. SD rat model of subcutaneous glioma showed the initial of tumor formation, CD133+ cells scattered. With tumor growth, CD133+ cells began to tend to capillaries, in late distributed clusters in perivascular. Meanwhile as tumor growth, CD133 protein expression was gradually increased: the values of Western blot analysis of CD133 expression on 6, 9, 12, 15, 20 d were 0.208±0.004, 0.282±0.003, 0.360±0.004, 0.564±0.135, 0.756±0.007, the differences were significant between different groups (F=2601.681, P<0.01). At a high magnification, the CD133 scores with immunohistochemical staining on 6, 9, 12, 15 d were 0.8±0.4, 2.4±0.5, 4.0 ± 0.7, 6.0±0.7; HIF-1α scores were 0.8±0.4, 2.8±0.8, 5.0±0.7, 6.8±0.4. By Spearman rank correlation analysis found that the relationship between CD133 and HIF-1α expression was positively correlated (r=0.921, P<0.01).
Glioma stem cells promote angiogenesis more than non-stem cells; HIF-1α and its downstream gene product might mediate the distribution of glioma stem cells around the perivascular.
动态观察胶质瘤干细胞如何促进肿瘤形成和血管生成,并研究皮下肿瘤不同生长阶段胶质瘤干细胞分布与微血管之间的相关性。
采用干细胞培养基培养和磁激活细胞分选技术从C6大鼠胶质瘤细胞系中获取CD133+细胞。建立Sprague Dawley(SD)大鼠耳部模型观察胶质瘤干细胞促进血管形成。利用C6皮下胶质瘤模型及缺氧诱导因子-1α(HIF-1α)和CD133免疫组化染色研究胶质瘤干细胞分布与微血管的关系。采用蛋白质印迹法检测皮下肿瘤各阶段CD133蛋白表达。
成功从C6胶质瘤细胞系中分离鉴定出胶质瘤干细胞,耳部模型的建立实现了对CD133+细胞参与血管生成和肿瘤形成的实时动态观察。SD大鼠皮下胶质瘤模型显示肿瘤形成初期,CD133+细胞散在分布。随着肿瘤生长,CD133+细胞开始向毛细血管靠拢,后期在血管周围呈簇状分布。同时随着肿瘤生长,CD133蛋白表达逐渐增加:蛋白质印迹法分析CD133在第6、9、12、15、20天的表达值分别为0.208±0.004、0.282±0.003、0.360±0.004、0.564±0.135、0.756±0.007,不同组间差异有统计学意义(F=2601.681,P<0.01)。高倍镜下,免疫组化染色CD133评分在第6、9、12、15天分别为0.8±0.4、2.4±0.5、4.0±0.7、6.0±0.7;HIF-1α评分分别为0.8±0.4、2.8±0.8、5.0±0.7、6.8±0.4。经Spearman等级相关分析发现,CD133与HIF-1α表达呈正相关(r=0.921,P<0.01)。
胶质瘤干细胞比非干细胞更能促进血管生成;HIF-1α及其下游基因产物可能介导胶质瘤干细胞在血管周围的分布。