Sundell-Bergman S, Johanson K J, Wlodek D
Acta Radiol Oncol. 1982;21(6):455-9. doi: 10.3109/02841868209134327.
The induction and repair of DNA strand breaks induced by disintegration of 3H and 125I incorporated into DNA was examined by the DNA unwinding technique in two strains of murine L5178Y lymphoma cells. The L5178Y-S cells are extremely sensitive to decay of 3H incorporated into DNA, L5178Y-R cells have rather 'normal' sensitivity. The number of strand breaks induced during a cold treatment was about 2.2 per 3H decay and 4 per 125I decay. No differences were found between the two strains. During the labelling period accumulation of unrepaired DNA strands occurred. About 80 per cent of all 125I induced DNA strand breaks was left unrepaired after a 21 h labelling period. No differences occurred between the two cell strains. It thus seems that the marked difference between the two cell strains in sensitivity to decay of the nuclides incorporated into DNA is not due to differences in the rejoining capacity of DNA strand breaks.
采用DNA解旋技术,在两株小鼠L5178Y淋巴瘤细胞中检测了掺入DNA的³H和¹²⁵I衰变所诱导的DNA链断裂的诱导与修复情况。L5178Y - S细胞对掺入DNA的³H衰变极其敏感,L5178Y - R细胞具有相当“正常”的敏感性。冷处理期间诱导的链断裂数量约为每一次³H衰变2.2个,每一次¹²⁵I衰变4个。两株细胞之间未发现差异。在标记期间,未修复的DNA链出现积累。经过21小时的标记期后,所有¹²⁵I诱导的DNA链断裂中约80%未得到修复。两株细胞系之间未出现差异。因此,两株细胞系对掺入DNA的核素衰变敏感性的显著差异似乎并非由于DNA链断裂再连接能力的差异所致。