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电离辐射对共济失调毛细血管扩张症细胞周期进程的影响。

The effects of ionizing radiation on cell cycle progression in ataxia telangiectasia.

作者信息

Ford M D, Martin L, Lavin M F

出版信息

Mutat Res. 1984 Jan;125(1):115-22. doi: 10.1016/0027-5107(84)90038-1.

Abstract

Although ataxia telangiectasia (AT) cells are more sensitive than normal cells to killing by ionizing radiation, their DNA synthesis is more resistant to inhibition by radiation. It was thought that this anomaly in DNA synthesis was likely to perturb cell cycle progression. Flow cytometry and the fraction of labelled mitoses (FLM) were used to investigate effects of irradiation in normal and AT cell lines. The FLM indicated that radiation apparently induced a longer G2 delay in normal cells than in AT cells. However, flow cytometry showed that radiation induced much larger and more prolonged increases in the proportion of G2 cells in AT than in normals. AT populations also showed much larger postirradiation decreases in viable cell numbers. These data suggest that a large proportion of the radiosensitive AT cells are not reversibly blocked in G2 but die there, and never proceed through mitosis. The less radiosensitive normal cells are delayed in G2 and then proceed through mitosis. We suggest that the apparently shorter radiation-induced mitotic delay seen in AT cells by FLM is not real but is an artifact arising from perturbation of steady state conditions by selective elimination of a particular cohort of AT cells. Accumulation of AT cells in G2 is compatible with radiosensitivity of these cells and may arise from a defect in DNA repair or an anomaly in DNA replication.

摘要

虽然共济失调毛细血管扩张症(AT)细胞比正常细胞对电离辐射杀伤更敏感,但其DNA合成对辐射抑制更具抗性。曾认为DNA合成中的这种异常可能会扰乱细胞周期进程。采用流式细胞术和标记有丝分裂分数(FLM)来研究辐射对正常细胞系和AT细胞系的影响。FLM表明,辐射在正常细胞中诱导的G2期延迟显然比在AT细胞中更长。然而,流式细胞术显示,辐射诱导的AT细胞中G2期细胞比例的增加比正常细胞大得多且持续时间更长。AT细胞群体在辐射后活细胞数量的减少也大得多。这些数据表明,大部分对辐射敏感的AT细胞并非在G2期被可逆性阻滞,而是在该阶段死亡,且从未进入有丝分裂。对辐射较不敏感的正常细胞在G2期延迟,然后进入有丝分裂。我们认为,通过FLM在AT细胞中看到的明显较短的辐射诱导有丝分裂延迟并非真实情况,而是由于选择性消除特定群体的AT细胞扰乱了稳态条件而产生的假象。AT细胞在G2期的积累与这些细胞的辐射敏感性相符,可能源于DNA修复缺陷或DNA复制异常。

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