Oleinick N L, Evans H H
Radiat Res. 1985 Jan;101(1):29-46.
The activity of poly(ADP-ribose) polymerase is stimulated by DNA damage resulting from treatment of cells with ionizing radiation, as well as with DNA-damaging chemicals. The elevated polymerase activity can be observed at doses lower than those necessary for measurable reduction in cellular NAD concentration (less than 20 Gy). Several nuclear proteins, including the polymerase itself, are poly(ADP-ribosylated) at elevated levels in irradiated Chinese hamster cells. The addition of inhibitors of poly(ADP-ribose) polymerase to irradiated cells has been found to sensitize the cells to the lethal effects of the radiation, to inhibit the repair of potentially lethal damage, and to delay DNA strand break rejoining. Because of the nonspecificity of the inhibitors, however, it is as yet unknown whether their effects are directly related to the inhibition of poly(ADP-ribose) polymerase, to interference with the poly(ADP-ribosylation) of one or more chromosomal proteins, or to effects unrelated to the poly(ADP-ribosylation) process. The data are consistent with the involvement of poly(ADP-ribose) in the repair of radiation damage, but the nature of this involvement remains to be elucidated.
聚(ADP - 核糖)聚合酶的活性可被电离辐射以及DNA损伤化学物质处理细胞所导致的DNA损伤刺激。在低于可测量细胞NAD浓度降低所需剂量(小于20 Gy)时即可观察到聚合酶活性升高。在受辐照的中国仓鼠细胞中,包括聚合酶本身在内的几种核蛋白会以升高的水平发生聚(ADP - 核糖基化)。已发现向受辐照细胞中添加聚(ADP - 核糖)聚合酶抑制剂会使细胞对辐射的致死效应敏感,抑制潜在致死损伤的修复,并延迟DNA链断裂重连。然而,由于抑制剂的非特异性,目前尚不清楚它们的作用是直接与聚(ADP - 核糖)聚合酶的抑制有关,还是与干扰一种或多种染色体蛋白的聚(ADP - 核糖基化)有关,亦或是与聚(ADP - 核糖基化)过程无关的效应。这些数据与聚(ADP - 核糖)参与辐射损伤修复一致,但这种参与的性质仍有待阐明。