Djordjevic B, Tolmach L J
Laboratory of Radiation Biology, Mallinckrodt Institute of Radiology, School of Medicine,
Biophys J. 1967 Jan;7(1):77-94. doi: 10.1016/S0006-3495(67)86576-7. Epub 2008 Dec 31.
The sensitivity of HeLa S3 cells to 220 kv X-rays was measured in terms of cell survival (colony development) during the G2 phase of the cell generation cycle, employing two procedures designed to free G2 cultures from contaminating cells from other phases of the cycle. Treatment of synchronous cultures (obtained initially by mitotic selection) with high specific activity tritiated thymidine (HSA-(3)HTdR) selectively eliminated S phase cells, while addition of vinblastine permitted removal of cells as they entered mitosis. It was found that HeLa S3 cells become increasingly sensitive as they progress through G2. The pattern of sensitivity fluctuations observed in synchronous HeLa S3 populations selected by the foregoing method was compared with that found in synchronous cultures prepared by the HSA-(3)HTdR method of Whitmore. The latter method had been used previously with mouse L cells, which were found to undergo a different pattern of sensitivity fluctuations. The two methods yield similar results for HeLa cells in the S and G2 phases of the cycle. It may be concluded, therefore, that the discrepancies between HeLa and mouse L cells do not arise from methodological factors, but represent fundamental differences between the cell types.
通过两种旨在使处于G2期的培养物不含细胞周期其他阶段污染细胞的方法,根据细胞存活(集落形成)情况测定了HeLa S3细胞对220千伏X射线的敏感性。用高比活度的氚标记胸腺嘧啶核苷(HSA-(3)HTdR)处理同步培养物(最初通过有丝分裂选择获得)可选择性地消除S期细胞,而加入长春花碱则可在细胞进入有丝分裂时将其去除。结果发现,HeLa S3细胞在G2期进程中敏感性逐渐增加。将通过上述方法选择的同步HeLa S3群体中观察到的敏感性波动模式与通过Whitmore的HSA-(3)HTdR方法制备的同步培养物中发现的模式进行了比较。后一种方法先前已用于小鼠L细胞,发现其经历了不同的敏感性波动模式。对于处于细胞周期S期和G2期的HeLa细胞,这两种方法产生相似的结果。因此,可以得出结论,HeLa细胞和小鼠L细胞之间的差异并非源于方法学因素,而是代表了细胞类型之间的根本差异。