Olive P L, Banáth J P, Durand R E
Medical Biophysics Department, British Columbia Cancer Research Centre, Vancouver, Canada.
Radiat Res. 1996 Dec;146(6):595-602.
The TK6 and WI-L2-NS human lymphoblast cell lines are derived from the same donor, but WI-L2-NS cells are more resistant to killing by ionizing radiation and also contain a mutation in the coding region of the p53 gene which delays the appearance of apoptosis. To determine whether the difference in radiosensitivity is a result of the slower rate of appearance of apoptosis (referred to as the rate of apoptosis) or to other factors related to the function of p53 such as the G1-phase checkpoint, we have examined the clonogenicity and rates of apoptosis in synchronous populations of these two cell lines as a function of time after exposure to x-rays. The greater radiosensitivity of G1-phase TK6 cells compared to G1-phase WI-L2-NS cells appeared adequate to explain the difference in radiosensitivity of asynchronous cultures. However, TK6 cells irradiated in G1 phase underwent apoptosis about three times more slowly than cells irradiated in other phases of the cycle, cautioning against equating more rapid apoptosis with greater radiosensitivity. The slower rate of apoptosis of G1-phase TK6 cells could not be explained by a radiation-induced block in G1 phase since there was only a short delay in exit of cells from G1 phase. Giant cells (primarily polyploid) were formed after irradiation of WI-L2-NS but not TK6 cells, and fewer giant cells were observed 3-4 days after irradiation in WI-L2-NS cells irradiated in S phase than cells irradiated in other phases. Giant cells were lost from the population through apoptosis which occurred in a synchronous fashion in the multiple nuclei. These results highlight interesting differences in the pattern of cell death between the two cell lines and suggest that the response of TK6 cells in G1 phase, which has the slowest rate of appearance of apoptosis in spite of the fact that it is the most radiosensitive phase for clonogenic survival, may be largely responsible for the reduced shoulder on the radiation survival curve for TK6 cells compared with WI-L2-NS cells.
TK6和WI-L2-NS人淋巴母细胞系源自同一供体,但WI-L2-NS细胞对电离辐射杀伤的抵抗力更强,并且其p53基因编码区存在一个突变,该突变会延迟细胞凋亡的出现。为了确定放射敏感性的差异是由于凋亡出现速率较慢(称为凋亡率),还是由于与p53功能相关的其他因素,如G1期检查点,我们检测了这两种细胞系同步群体在接受X射线照射后不同时间的克隆形成能力和凋亡率。与G1期的WI-L2-NS细胞相比,G1期的TK6细胞具有更高的放射敏感性,这似乎足以解释非同步培养物放射敏感性的差异。然而,在G1期受到照射的TK6细胞发生凋亡的速度比在细胞周期其他阶段受到照射的细胞慢约三倍,这提醒我们不能将更快的凋亡等同于更高的放射敏感性。G1期TK6细胞凋亡速率较慢不能用G1期的辐射诱导阻滞来解释,因为细胞从G1期退出仅有短暂延迟。WI-L2-NS细胞照射后形成了巨细胞(主要是多倍体),而TK6细胞未形成,并且在S期受到照射的WI-L2-NS细胞中,照射后3 - 4天观察到的巨细胞比在其他阶段受到照射的细胞少。巨细胞通过多核中同步发生的凋亡从群体中消失。这些结果突出了两种细胞系在细胞死亡模式上的有趣差异,并表明G1期TK6细胞的反应可能在很大程度上导致了与WI-L2-NS细胞相比,TK6细胞辐射存活曲线上的肩部降低,尽管G1期是克隆存活最放射敏感的阶段,但却是凋亡出现速率最慢的阶段。