Jeong J K, Dybing E, Søderlund E, Brunborg G, Holme J A, Lau S S, Monks T J
Division of Pharmacology and Toxicology, College of Pharmacy, University of Texas at Austin 78712, USA.
Arch Biochem Biophys. 1997 May 15;341(2):300-8. doi: 10.1006/abbi.1997.9969.
2-Bromo-bis-(glutathion-S-yl)hydroquinone [2-Br-bis-(GSyl)HQ] causes DNA single-strand breaks (SSB), causes growth arrest, induces the expression of gadd153 (a gene inducible by growth arrest and DNA damage), and decreases histone H2B mRNA in log-phase renal proximal tubular epithelial cells (LLC-PK1). Renal epithelial cells in vivo normally exhibit a low mitotic index, therefore experiments in both plateau- and log-phase cells are necessary for a comprehensive understanding of the stress response to 2-Br-bis-(GSyl)HQ. In the present article we demonstrate that not all features of the stress response in log-phase cells are reproduced in plateau-phase cells. Thus, although 2-Br-bis-(GSyl)HQ causes concentration and time-dependent increases in DNA SSB, and increases the expression of gadd153, histone H2B mRNA levels are unaltered in plateau-phase cells. The relationship between reactive oxygen species, DNA damage, gene expression, and cytotoxicity was also investigated. Our findings suggest that (i) 2-Br-bis-(GSyl)HQ-mediated DNA damage in LLC-PK1 cells is mediated by the generation of H2O2; (ii) DNA damage, either directly or indirectly, contributes to cell death; and (iii) DNA damage, either directly or indirectly, provides the initial signal for gadd153 expression. In addition, DNA repair is rapid in LLC-PK1 cells, and the DNA-repair inhibitors 1-beta-D-arabinofuranosylcytosine and hydroxyurea have no effect on the amount of DNA SSB. Although the addition of 3-aminobenzamide following 2-Br-bis-(GSyl)HQ exposure has no effect on the removal of DNA SSB, it causes a slight but significant increase in gadd153 expression and cell viability, indicating that activation of poly(ADP-ribose)polymerase may exacerbate toxicity. Finally, aurintricarboxylic acid did not prevent DNA SSB or cytotoxicity in 2-Br-bis-(GSyl) HQ-treated LLC-PK1 cells, implying that activation of endonucleases does not play a role in these processes.
2-溴-双(谷胱甘肽-S-基)对苯二酚[2-Br-双(GSyl)HQ]可导致DNA单链断裂(SSB),引起生长停滞,诱导gadd153(一种可由生长停滞和DNA损伤诱导的基因)的表达,并降低对数期肾近端小管上皮细胞(LLC-PK1)中的组蛋白H2B mRNA水平。体内肾上皮细胞通常表现出较低的有丝分裂指数,因此,为了全面了解对2-Br-双(GSyl)HQ的应激反应,对数期细胞和平稳期细胞的实验都是必要的。在本文中,我们证明了并非对数期细胞应激反应的所有特征都会在平稳期细胞中重现。因此,尽管2-Br-双(GSyl)HQ会导致DNA SSB随浓度和时间依赖性增加,并增加gadd153的表达,但平稳期细胞中的组蛋白H2B mRNA水平并未改变。我们还研究了活性氧、DNA损伤、基因表达和细胞毒性之间的关系。我们的研究结果表明:(i)LLC-PK1细胞中2-Br-双(GSyl)HQ介导的DNA损伤是由H2O2的产生介导的;(ii)DNA损伤直接或间接导致细胞死亡;(iii)DNA损伤直接或间接为gadd153表达提供初始信号。此外,LLC-PK1细胞中的DNA修复很快,DNA修复抑制剂1-β-D-阿拉伯呋喃糖基胞嘧啶和羟基脲对DNA SSB的量没有影响。尽管在2-Br-双(GSyl)HQ暴露后添加3-氨基苯甲酰胺对DNA SSB的去除没有影响,但它会导致gadd153表达和细胞活力略有但显著增加,表明聚(ADP-核糖)聚合酶的激活可能会加剧毒性。最后,金精三羧酸并不能预防2-Br-双(GSyl)HQ处理的LLC-PK1细胞中的DNA SSB或细胞毒性,这意味着核酸内切酶的激活在这些过程中不起作用。