表达增强型绿色荧光蛋白的骨肉瘤细胞亚株建立及生物学特性  

Establishment of MG63 cells subline expressing enhanced green fluorescent protein gene and biological characteristics

作　　者：李新志[1] 陈安民[1] 郭风劲[1] 罗正强[1] 

机构地区：[1]华中科技大学同济医学院附属同济医院骨科,武汉430030

出　　处：《中华实验外科杂志》2006年第9期1112-1114,共3页Chinese Journal of Experimental Surgery

基　　金：国家重点基础研究规划发展规划973项目(2002CB513107)

摘　　要：目的建立经绿色荧光蛋白基因转染的骨肉瘤细胞亚株并研究其生物特性。方法利用脂质体转染增强型绿色荧光蛋白真核表达质粒(pEGFP-N1)人人骨肉瘤MG63细胞系,通过有限稀释法和细胞电泳,获得两株细胞克隆M6和M8,经体外细胞增殖、软琼脂形成、生长曲线、裸鼠成瘤试验综合分析其生物学行为改变。应用组织形态学观察、染色体分析、软琼脂克隆形成法研究癌细胞的生物学特性。结果M6和M8两株在细胞电泳率和侵袭性上差异有统计学意义(P＜0．05),其中M6的群体倍增时间为38．4 h,软琼脂形成率为18．7%,M8群体倍增时间为23．0 h,软琼脂形成率为29．3%。裸小鼠背部皮下接种M6和M8,发现M8成瘤时间短,细胞增殖快,但在4周内两者均不发生转移。结论骨肉瘤细胞亚系有不同的转移特性,GFP的整合及表达未对MG63细胞的生长状态造成明显影响,可作为报告基因进一步了解骨肉瘤细胞转移的差异性分析。Objective To establish the MG63 cells subline trasnfected with enhanced GFP gene and study its biological characteristics. Methods After MG63 cells were transfected by enhanced GFP gene in liposome-mediated gene transfer, single cell clones were isolated using limited dilution method. Through preliminary electrolShoretic technique and spontaneous metastasis assay in nude mice, two cloned MG63 cell sublines （M6, M8 ） were selected for further observation on morphology, chromosome number, in vitro growth and invasion assays in nude mice. Results There was difference in electrophoretic mobility and in vitro invasive abilities between M6 and M8. The population doubling time of M6 and M8 was 38.4 h and 23.0 h respectively,rate of colonies was 18.7 % and 29.3 % respectively. But there were no obvious differences in other biological features between the two sublines. Conclusion MG63 cell line consists of different subpopulations of cells with different metastatic properties. These sublines transfected by EGFP may be valuable for further study on the molecular mechanisms of cancer metastasis.

关 键 词：骨肉瘤 转移 绿色荧光蛋白 生物学 

分 类 号：R738.1[医药卫生—肿瘤]