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人肺腺癌细胞系(LAC)中SP细胞亚群的分选及其干细胞特性分析
引用本文:潘 旋,李艳利,德 伟,王科明,王朝霞. 人肺腺癌细胞系(LAC)中SP细胞亚群的分选及其干细胞特性分析[J]. 南京医科大学学报(自然科学版), 2010, 0(11): 1584-1589
作者姓名:潘 旋  李艳利  德 伟  王科明  王朝霞
作者单位:南京医科大学第二附属医院肿瘤科,江苏 南京 210011;南京医科大学生物化学与分子生物学系,江苏 南京 210029;南京医科大学生物化学与分子生物学系,江苏 南京 210029;南京医科大学第二附属医院肿瘤科,江苏 南京 210011;南京医科大学第二附属医院肿瘤科,江苏 南京 210011
基金项目:江苏省教育厅基金资助项目(07KJD320142);江苏省卫生厅基金资助项目(H200710)
摘    要:
目的: 分选人肺腺癌细胞系(LAC)中SP细胞(side population cells)亚群并分析其具有的干细胞特性?方法:运用流式细胞荧光激活分选技术(FACS)分选LAC中SP细胞亚群和非SP细胞亚群,利用MTT?体外克隆形成和皮下移植瘤试验分析其体内?外增殖能力,流式细胞仪分析细胞周期及细胞分化,RT-PCR方法检测其ATP结合盒转运蛋白(ABCG2)基因的表达情况?结果:流式细胞荧光激活分选结果显示:LAC中含有约1.88%的SP细胞亚群?MTT和体外克隆形成试验表明:SP细胞亚群的体外增殖能力显著强于非SP细胞亚群?同时,裸鼠皮下接种SP细胞亚群,其体内成瘤能力也要显著强于非SP细胞亚群?流式细胞仪分析结果表明:SP细胞亚群的G0/G1期比例显著高于非SP细胞(P < 0.05)?细胞分化实验结果表明:两个亚群中SP细胞比率分别为(1.46±0.08)%和(0.12±0.04)%?RT-PCR结果显示:ABCG2基因mRNA在SP细胞亚群中的表达水平是其在非SP细胞亚群中的3.3倍(P < 0.05)?结论:利用LAC中SP细胞亚群具有肺癌干细胞的特性,流式细胞荧光激活分选肺腺癌SP细胞亚群可能是分离肺腺癌干细胞的有效方法?

关 键 词:肺腺癌   肿瘤干细胞   SP细胞   流式细胞荧光激活分选技术
收稿时间:2010-05-13

Characterization of side population(SP) of stem-like tumor cells in human lung adenocarcinoma cell line(LAC)
PAN Xuan,LI Yan-li,DE Wei,WANG Ke-ming and WANG Zhao-xia. Characterization of side population(SP) of stem-like tumor cells in human lung adenocarcinoma cell line(LAC)[J]. Acta Universitatis Medicinalis Nanjing, 2010, 0(11): 1584-1589
Authors:PAN Xuan  LI Yan-li  DE Wei  WANG Ke-ming  WANG Zhao-xia
Affiliation:Department of Oncology,the Second Affiliated Hospital of NJMU,Nanjing 210011;Department of Biochemistry and Molecular Biology,NJMU,Nanjing 210029,China;Department of Biochemistry and Molecular Biology,NJMU,Nanjing 210029,China;Department of Oncology,the Second Affiliated Hospital of NJMU,Nanjing 210011;Department of Oncology,the Second Affiliated Hospital of NJMU,Nanjing 210011
Abstract:
Objective: To explore a feasible method to detect tumor stem-like cells in human lung adenocarcinoma cells(LAC),and to analyze the properties of the sorted side population(SP)cells. Methods:Fluorescence-activated cell sorting assay(FACS)was performed to sort the SP and non-SP cells of LAC. MTT,colony formation and in vivo tumorigenesis assays were performed to analyze the proliferation capacity of SP and non-SP cells in vitro and in vivo. Flow cytometric assay was performed to detect the cell cycle and differentiation of SP cells. RT-PCR assay was performed to detect the expression of ATP-binding cassette transporter G2(ABCG2) mRNA in SP and non-SP cells. Results:Results from FACS showed that SP cells were detected in approximately 1.88% of LAC. MTT and in vitro colony formation assays showed that the in vitro proliferation capacity of SP cells was significantly stronger than that of non-SP cells. Additionally,the in vivo tumorigenesis capacity of SP cells was significantly stronger than that of non-SP cells. Cell cycle analysis indicated that the cell number of G0/G1 phase in SP cells was higher than that in non-SP cells(P < 0.05). The rates of SP cells in SP and non-SP populations were approximately (1.46±0.08)% and (0.12±0.04)%,respectively. Moreover,the level of ABCG2 mRNA in SP cells was 3.3 times of that in non-SP cells(P < 0.05). Conclusion:The SP cells sorted from LAC possessed characteristics of cancer stem-like cells,and SP cells sorted by FACS could be an effective method used to sort lung cancer stem cells.
Keywords:lung adenocarcinoma   cancer stem cell   side population cells   fluorescence-activated cell sorting
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