Biaglow J E, Varnes M E, Tuttle S W, Oleinick N L, Glazier K, Clark E P, Epp E R, Dethlefsen L A
Int J Radiat Oncol Biol Phys. 1986 Jul;12(7):1139-42. doi: 10.1016/0360-3016(86)90244-0.
Our data show that A549 cells are increasingly radiosensitive with prolonged exposure to L-BSO. The resulting glutathione and protein thiol depleted cells show both loss of shoulder and slope modification. Furthermore, there is an increase in single strand DNA breaks and irrepairable cross-linking. The aerobic radiation damage in the thiol depleted state appears to be different from that obtained with hypoxic cells. Any postulated role for GSH in reducing or preventing peroxidative radiation damage must also include protection against single strand DNA breaks as well as involvement in repairing DNA-protein cross-links. The latter effect may be related to decreased protein thiol content as reflected in a decreased enzyme capacity to repair DNA damage.
我们的数据表明,随着暴露于L - BSO时间的延长,A549细胞的放射敏感性逐渐增加。由此导致的谷胱甘肽和蛋白质巯基耗尽的细胞表现出肩区丧失和斜率改变。此外,单链DNA断裂和不可修复的交联增加。巯基耗尽状态下的需氧辐射损伤似乎与缺氧细胞的不同。谷胱甘肽在减少或预防过氧化辐射损伤中任何假定的作用,都必须包括对单链DNA断裂的保护以及参与修复DNA - 蛋白质交联。后一种效应可能与蛋白质巯基含量降低有关,这反映在修复DNA损伤的酶能力下降。