Saunders E L, Meredith M J, Eisert D R, Freeman M L
Vanderbilt Center for Radiation Oncology, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.
Radiat Res. 1991 Mar;125(3):267-76.
The relationship between the intracellular glutathione (GSH) concentration and the aerobic radiation response was studied in Chinese hamster ovary cells. Various degrees of GSH depletion were produced by exposure to buthionine sulfoximine (BSO) and/or diethyl maleate (DEM). Diethyl maleate did not act as a classical radiosensitizer under the experimental conditions employed, nor did exposure to DEM/BSO nonspecifically affect protein thiols as measured by thiol blotting. Dose-response curves were obtained using cells irradiated in the absence or presence of DEM/BSO, which decreased GSH levels by 90-95%. Exposure to DEM/BSO did not affect the formation of DNA single-strand breaks or DNA-protein crosslinks measured immediately after irradiation performed at ice temperatures. Analysis of survival curves indicated that the Dq was decreased by 18% when GSH depletion occurred prior to, during, and after irradiation. The DEM/BSO exposure did not affect D0. To study postirradiation conditions, cells were exposed to 10 microM DEM prior to and during irradiation, which was performed at ice temperatures. Levels of GSH were depleted by 75% by this protocol. Immediately after irradiation, the cells were rapidly warmed by the addition of 37 degrees C growth medium containing either 10 or 90 microM DEM. Addition of 10 microM DEM after irradiation did not affect the degree of depletion, which remained constant at 75%. In contrast, GSH depletion was increased to 90% 10 min after addition of the 90 microM DEM. Addition of 90 microM DEM after irradiation produced a statistically significant difference in survival compared to addition of 10 microM DEM. In a second depletion protocol, cells were exposed to 100 microM DEM at room temperature for 5 min, irradiated, incubated at 37 degrees C for 1 h, washed, and then incubated in 50 microM BSO for 24 h. This depletion protocol reduced survival by a factor of 2.6 compared to cells not exposed to the combination of DEM/BSO. Survival was not affected if the cells were exposed to the DEM or BSO alone. This was interpreted to indicate that survival was not affected by GSH depletion occurring after irradiation unless depletion was rapid and sustained. The rate of repair of sublethal and potentially lethal damage was measured and found to be independent of the DEM/BSO exposure. These experimental results in addition to previous ones (Freeman and Meredith, Int. J. Radiat. Oncol. Biol. Phys. 13, 1371-1375, 1987) were interpreted to indicate that under aerobic conditions GSH depletion may alter the expression of radiation damage by affecting metabolic fixation.
在中国仓鼠卵巢细胞中研究了细胞内谷胱甘肽(GSH)浓度与有氧辐射反应之间的关系。通过暴露于丁硫氨酸亚砜胺(BSO)和/或马来酸二乙酯(DEM)产生不同程度的GSH耗竭。在所用实验条件下,马来酸二乙酯不作为经典的放射增敏剂,通过硫醇印迹法测定,暴露于DEM/BSO也不会非特异性地影响蛋白质硫醇。使用在不存在或存在DEM/BSO的情况下照射的细胞获得剂量反应曲线,DEM/BSO使GSH水平降低90 - 95%。暴露于DEM/BSO不影响在冰温下照射后立即测量的DNA单链断裂或DNA - 蛋白质交联的形成。存活曲线分析表明,当在照射前、照射期间和照射后发生GSH耗竭时,Dq降低了18%。DEM/BSO暴露不影响D0。为了研究照射后的情况,在冰温下照射前和照射期间将细胞暴露于10μM DEM。通过该方案使GSH水平降低75%。照射后立即通过添加含有10或90μM DEM的37℃生长培养基使细胞快速升温。照射后添加10μM DEM不影响耗竭程度,其保持在75%不变。相比之下,添加90μM DEM后10分钟GSH耗竭增加到90%。与添加10μM DEM相比,照射后添加90μM DEM在存活方面产生了统计学上的显著差异。在第二个耗竭方案中,将细胞在室温下暴露于100μM DEM 5分钟,照射,在37℃孵育1小时,洗涤,然后在50μM BSO中孵育24小时。与未暴露于DEM/BSO组合的细胞相比,该耗竭方案使存活率降低了2.6倍。如果细胞单独暴露于DEM或BSO,存活率不受影响。这被解释为表明照射后发生的GSH耗竭不会影响存活,除非耗竭迅速且持续。测量了亚致死和潜在致死损伤的修复率,发现其与DEM/BSO暴露无关。这些实验结果以及先前的结果(Freeman和Meredith,《国际放射肿瘤学、生物学和物理学杂志》13,1371 - 1375,1987)被解释为表明在有氧条件下,GSH耗竭可能通过影响代谢固定来改变辐射损伤表现。