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HeLa cells and their possible contamination of other cell lines: Karyotype studies

机译:HeLa细胞及其对其他细胞系的可能污染:核型研究

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G- and C-banding techniques were applied to the chromosomes of 5 human cell lines, viz. HeLa, KB, HEp-2, D98/AH-2 and Lu106. According to the records, the 3 former ones are of tumor origin. the 2 latter of normal origin. The 5 cell lines showed considerable similarities: (1) their stemline chromosome numbers were near-triploid; (2) the normal chromosome types. generally present in disomic or trisomic numbers, showed the same deviations through 4 or all 5 lines: nulli- or monosomy in No. 3, tri- or tetrasomy in No. 7, 15 and 17, maximum variation in No. 7, 9 and 16, no Y chromosome in spite of the supposedly male origin of some of the lines; (3) the incidence of markers was of comparable size order (21–25% in KB, HeLa and D98/AH-2, 29% in HEp-2, 36% in Lu106); (4) the majority of the marker types were found either in relatively low or high frequencies (1–3 or 8–10 out of 10 cells); (5) marker chromosomes of concordant band pattern were common to different lines; (6) the total lengths of normal and marker chromosomes and whole complements were approximately the same in most or all lines. These results indicate that the variability in the parameters analyzed is less than expected in completely independent lines. The conclusion is that all 5 cell lines are most likely of HeLa origin.
机译:G带和C带技术应用于5种人类细胞系的染色体,即。 HeLa,KB,HEp-2,D98 / AH-2和Lu106。根据记录,前三个是肿瘤起源。正常来源的第二个。这5个细胞系显示出相当的相似性:(1)它们的干系染色体数目接近三倍体; (2)正常的染色体类型。通常以二体组或三体组数出现,在4条或全部5条线中显示相同的偏差:3号无效或单体,7、15和17号的三体或四体,7、9和7号的最大变异。 16,尽管某些品系据说是男性起源,但没有Y染色体; (3)标记物的发生率具有可比的大小顺序(KB,HeLa和D98 / AH-2中21–25%,HEp-2中29%,Lu106中36%); (4)大多数标记物类型以相对较低或较高的频率出现(每10个细胞中有1-3个或8-10个细胞); (5)不同谱带共有一致带状标记染色体。 (6)在大多数或所有品系中,正常和标记染色体以及整个补体的总长度大致相同。这些结果表明,在完全独立的谱系中,所分析参数的变异性小于预期。结论是所有5种细胞系均最有可能是HeLa起源的。

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