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聚(ADP-核糖)聚合酶抑制剂可维持DNA损伤细胞中的烟酰胺腺嘌呤二核苷酸和三磷酸腺苷水平:刺激非预定DNA合成的机制

Poly(ADP-ribose) Polymerase inhibitors preserve nicotinamide adenine dinucleotide and adenosine 5'-triphosphate pools in DNA-damaged cells: mechanism of stimulation of unscheduled DNA synthesis.

作者信息

Sims J L, Berger S J, Berger N A

出版信息

Biochemistry. 1983 Oct 25;22(22):5188-94. doi: 10.1021/bi00291a019.

Abstract

Inhibitors of poly(ADP-ribose) polymerase stimulated the level of DNA, RNA, and protein synthesis in DNA-damaged L1210 cells but had negligible effects in undamaged L1210 cells. The poly(ADP-ribose) polymerase inhibitors stimulated DNA repair synthesis after cells were exposed to high concentrations of N-methyl-N'-nitro-N-nitrosoguanidine (68 and 136 microM) but not after exposure to low concentrations (13.6 and 34 microM). When the L1210 cells were exposed to 136 microM N-methyl-N'-nitro-N-nitrosoguanidine, the activation of poly(ADP-ribose) polymerase resulted in the rapid depletion of oxidized nicotinamide adenine dinucleotide (NAD+) levels and subsequent depletion of adenosine 5'-triphosphate (ATP) pools. After low doses of N-methyl-N'-nitro-N-nitrosoguanidine (13.6 microM), there were only small decreases in NAD+ and ATP. Poly(ADP-ribose) polymerase inhibitors prevented the rapid fall in NAD+ and ATP pools. This preservation of the ATP pool has a permissive effect on energy-dependent functions and accounts for the apparent stimulation of DNA, RNA, and protein synthesis. Thus, the mechanism by which poly(ADP-ribose) polymerase inhibitors stimulate DNA, RNA, and protein synthesis in DNA-damaged cells appears to be mediated by their ability to prevent the drastic depletion of NAD+ pools that occurs in heavily damaged cells, thereby preserving the cells' ability to generate ATP and maintain energy-dependent processes.

摘要

聚(ADP - 核糖)聚合酶抑制剂可刺激DNA受损的L1210细胞中DNA、RNA和蛋白质的合成水平,但对未受损的L1210细胞影响可忽略不计。在细胞暴露于高浓度的N - 甲基 - N'-硝基 - N - 亚硝基胍(68和136 microM)后,聚(ADP - 核糖)聚合酶抑制剂可刺激DNA修复合成,但在暴露于低浓度(13.6和34 microM)后则无此作用。当L1210细胞暴露于136 microM N - 甲基 - N'-硝基 - N - 亚硝基胍时,聚(ADP - 核糖)聚合酶的激活导致氧化型烟酰胺腺嘌呤二核苷酸(NAD +)水平迅速耗尽,随后三磷酸腺苷(ATP)池也耗尽。在低剂量的N - 甲基 - N'-硝基 - N - 亚硝基胍(13.6 microM)作用后,NAD +和ATP仅有小幅下降。聚(ADP - 核糖)聚合酶抑制剂可防止NAD +和ATP池的快速下降。ATP池的这种保存对能量依赖性功能具有允许作用,并解释了DNA、RNA和蛋白质合成的明显刺激。因此,聚(ADP - 核糖)聚合酶抑制剂在DNA受损细胞中刺激DNA、RNA和蛋白质合成的机制似乎是通过其防止在严重受损细胞中发生的NAD +池急剧消耗的能力来介导的,从而保留细胞产生ATP并维持能量依赖过程的能力。

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