Hastings R J, Franks L M
Br J Cancer. 1983 Feb;47(2):233-44. doi: 10.1038/bjc.1983.31.
To study heterogeneity in a cell line derived from a human bladder carcinoma (EJ), 7 clones were isolated at low passage and examined for differences in culture behaviour, ability to grow in agar and tumorigenicity in nude mice. The parent EJ line had several distinct chromosome populations (both diploid and tetraploid), grew in agar and produced tumours in nude mice. Three of the clones had pseudodiploid modes and 4 had either hypo- or hypertetraploid modes. The 7 clones had 5 marker chromosomes in common but the combination of other marker chromosomes made each clone unique. No significant difference was found between the clones in the in vitro growth rate although analysis of in vitro culture behaviour showed heterogeneity in the pattern of cell movement on plastic substratum. Three clones were composed of static cells, one clone had very mobile cells; the other clones had rates of movement intermediate between the two. Differences were also found in the packing density of the cloned cells and in the cell size. All 7 clones grew in agar but heterogeneity was seen between the clones as shown by widely varying colony-forming efficiencies (0.5-13%). One clone had a high colony-forming ability in agar but failed to produce tumours in nude mice. The other clones were tumorigenic regardless of colony-forming efficiency in agar. Specific chromosome abnormalities were found to be associated with growth in agar and tumorigenicity but not with the growth pattern or the rate of movement of the cloned cells in culture.
为研究源自人膀胱癌(EJ)的细胞系中的异质性,在低传代时分离出7个克隆,并检测其培养行为、在琼脂中生长的能力以及在裸鼠中的致瘤性差异。亲本EJ细胞系有几个不同的染色体群体(二倍体和四倍体),能在琼脂中生长并在裸鼠中产生肿瘤。其中3个克隆具有假二倍体模式,4个具有亚四倍体或超四倍体模式。这7个克隆共有5条标记染色体,但其他标记染色体的组合使每个克隆都独一无二。尽管对体外培养行为的分析显示在塑料基质上细胞移动模式存在异质性,但各克隆之间在体外生长速率上未发现显著差异。3个克隆由静态细胞组成,1个克隆有非常活跃的细胞;其他克隆的移动速率介于两者之间。克隆细胞的堆积密度和细胞大小也存在差异。所有7个克隆都能在琼脂中生长,但克隆之间存在异质性,表现为集落形成效率差异很大(0.5 - 13%)。1个克隆在琼脂中有高集落形成能力,但在裸鼠中未能产生肿瘤。其他克隆无论在琼脂中的集落形成效率如何都具有致瘤性。发现特定的染色体异常与在琼脂中的生长和致瘤性相关,但与克隆细胞在培养中的生长模式或移动速率无关。