中华外科杂志
中華外科雜誌
중화외과잡지
CHINESE JOURNAL OF SURGERY
2012年
5期
452-456
,共5页
于圣平%杨学军%张斌%明浩朗%刘彬%刘志峰%任炳成%陈聪%高伟
于聖平%楊學軍%張斌%明浩朗%劉彬%劉誌峰%任炳成%陳聰%高偉
우골평%양학군%장빈%명호랑%류빈%류지봉%임병성%진총%고위
神经胶质瘤%肿瘤干细胞%新生血管化,病理性%疾病模型,动物
神經膠質瘤%腫瘤榦細胞%新生血管化,病理性%疾病模型,動物
신경효질류%종류간세포%신생혈관화,병이성%질병모형,동물
Glioma%Neoplastic stem cell%Neovascularizition,pathologic%Disease models,animal
目的 持续动态观察胶质瘤干细胞肿瘤生成和参与血管形成过程,研究不同生长阶段皮下移植瘤中干细胞分布与血管的关系.方法 干细胞培养基和免疫磁珠分选法获得C6细胞来源的CD133+细胞.建立CD133+细胞SD大鼠耳朵模型观察胶质瘤干细胞生成肿瘤及促进肿瘤血管形成情况.免疫组化染色研究不同生长阶段移植瘤中干细胞的分布与血管的关系及缺氧诱导因子-1α(HIF-1α)与这种分布的相关性.Western blot法检测各生长阶段肿瘤中CD133蛋白的表达情况.结果 成功分离和鉴定了C6细胞来源的CD133+细胞,并建立了SD大鼠耳朵模型可以实时动态的观察干细胞参与血管形成和肿瘤生成情况.SD大鼠皮下C6胶质瘤模型显示:在肿瘤形成的初期,CD133+细胞在肿瘤内散在分布,随着肿瘤的生长,CD133+细胞开始趋向于微血管,肿瘤生长的后期CD133+细胞在血管周成簇分布;同时随着肿瘤的生长,CD133蛋白的表达也随之增强,Western blot 检测接种后6、9、12、15、20d肿瘤中CD133表达量的吸光度值分别为0.208±0.004、0.282±0.003、0.360±0.004、0.564±0.135、0.756±0.007,各区域间的差异有统计学意义(F=2601.681,P<0.01).免疫组化染色显示接种6、9、12、15 d皮下移植瘤中CD133的表达分值为0.8±0.4、2.4±0.5、4.0±0.7、6.0±0.7,HIF-1α的分别为0.8±0.4、2.8±0.8、5.0±0.7、6.8±0.4;两者的表达量呈正相关(r =0.921,P<0.01).结论 胶质瘤干细胞比非干细胞更易形成肿瘤及参与肿瘤血管的形成,HIF-1α及其下游基因产物可能介导了胶质瘤干细胞围绕血管周分布.
目的 持續動態觀察膠質瘤榦細胞腫瘤生成和參與血管形成過程,研究不同生長階段皮下移植瘤中榦細胞分佈與血管的關繫.方法 榦細胞培養基和免疫磁珠分選法穫得C6細胞來源的CD133+細胞.建立CD133+細胞SD大鼠耳朵模型觀察膠質瘤榦細胞生成腫瘤及促進腫瘤血管形成情況.免疫組化染色研究不同生長階段移植瘤中榦細胞的分佈與血管的關繫及缺氧誘導因子-1α(HIF-1α)與這種分佈的相關性.Western blot法檢測各生長階段腫瘤中CD133蛋白的錶達情況.結果 成功分離和鑒定瞭C6細胞來源的CD133+細胞,併建立瞭SD大鼠耳朵模型可以實時動態的觀察榦細胞參與血管形成和腫瘤生成情況.SD大鼠皮下C6膠質瘤模型顯示:在腫瘤形成的初期,CD133+細胞在腫瘤內散在分佈,隨著腫瘤的生長,CD133+細胞開始趨嚮于微血管,腫瘤生長的後期CD133+細胞在血管週成簇分佈;同時隨著腫瘤的生長,CD133蛋白的錶達也隨之增彊,Western blot 檢測接種後6、9、12、15、20d腫瘤中CD133錶達量的吸光度值分彆為0.208±0.004、0.282±0.003、0.360±0.004、0.564±0.135、0.756±0.007,各區域間的差異有統計學意義(F=2601.681,P<0.01).免疫組化染色顯示接種6、9、12、15 d皮下移植瘤中CD133的錶達分值為0.8±0.4、2.4±0.5、4.0±0.7、6.0±0.7,HIF-1α的分彆為0.8±0.4、2.8±0.8、5.0±0.7、6.8±0.4;兩者的錶達量呈正相關(r =0.921,P<0.01).結論 膠質瘤榦細胞比非榦細胞更易形成腫瘤及參與腫瘤血管的形成,HIF-1α及其下遊基因產物可能介導瞭膠質瘤榦細胞圍繞血管週分佈.
목적 지속동태관찰효질류간세포종류생성화삼여혈관형성과정,연구불동생장계단피하이식류중간세포분포여혈관적관계.방법 간세포배양기화면역자주분선법획득C6세포래원적CD133+세포.건립CD133+세포SD대서이타모형관찰효질류간세포생성종류급촉진종류혈관형성정황.면역조화염색연구불동생장계단이식류중간세포적분포여혈관적관계급결양유도인자-1α(HIF-1α)여저충분포적상관성.Western blot법검측각생장계단종류중CD133단백적표체정황.결과 성공분리화감정료C6세포래원적CD133+세포,병건립료SD대서이타모형가이실시동태적관찰간세포삼여혈관형성화종류생성정황.SD대서피하C6효질류모형현시:재종류형성적초기,CD133+세포재종류내산재분포,수착종류적생장,CD133+세포개시추향우미혈관,종류생장적후기CD133+세포재혈관주성족분포;동시수착종류적생장,CD133단백적표체야수지증강,Western blot 검측접충후6、9、12、15、20d종류중CD133표체량적흡광도치분별위0.208±0.004、0.282±0.003、0.360±0.004、0.564±0.135、0.756±0.007,각구역간적차이유통계학의의(F=2601.681,P<0.01).면역조화염색현시접충6、9、12、15 d피하이식류중CD133적표체분치위0.8±0.4、2.4±0.5、4.0±0.7、6.0±0.7,HIF-1α적분별위0.8±0.4、2.8±0.8、5.0±0.7、6.8±0.4;량자적표체량정정상관(r =0.921,P<0.01).결론 효질류간세포비비간세포경역형성종류급삼여종류혈관적형성,HIF-1α급기하유기인산물가능개도료효질류간세포위요혈관주분포.
Objectives 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 mircovessels within different growth stages of subcutaneous tumor.Methods 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 mircovessels.Expressions of CD133 protein in each stage of the subcutaneous tumor were detected by Western blot.Results 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 ).Conclusions 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.