Kawamoto K, Herz F, Wolley R C, Hirano A, Koss L G
Virchows Arch B Cell Pathol Incl Mol Pathol. 1980;35(1):11-7. doi: 10.1007/BF02889145.
Analysis of DNA content in cultured cells derived from 5 benign and 8 malignant human brain tumors was performed by flow cytometry, using propidium iodide as fluorochrome. Normal, non-stimulated human lymphocytes were used as controls. Cells harvested from the first confluent subculture had DNA distribution histograms similar to those of a replicating, non-synchronous population of diploid cells. This observation was made on all cultures, regardless of the DNA distribution patterns in the original tumors, including two metastatic tumors which originally had a predominantly triploid DNA content. After 3 to 5 transfers an increase in the proportion of cells with a wide range of DNA content was observed in some cultures. These changes were usually associated with a loss of cell viability. These observations suggest that in the experimental setting described, in vitro proliferation of human tumor cells may be selectively associated with cells with diploid amounts of DNA.
使用碘化丙啶作为荧光染料,通过流式细胞术对源自5例良性和8例恶性人脑肿瘤的培养细胞中的DNA含量进行了分析。正常、未受刺激的人淋巴细胞用作对照。从首次汇合传代培养物中收获的细胞具有与二倍体细胞复制性、非同步群体相似的DNA分布直方图。在所有培养物中均观察到这一现象,无论原发肿瘤中的DNA分布模式如何,包括两个原发时主要为三倍体DNA含量的转移瘤。传代3至5次后,在一些培养物中观察到具有广泛DNA含量的细胞比例增加。这些变化通常与细胞活力丧失有关。这些观察结果表明,在所述的实验环境中,人肿瘤细胞的体外增殖可能与具有二倍体DNA量的细胞选择性相关。