Raaphorst G P, Bussey A, Thakar M, Bichay T, Ng C E
Ottawa Regional Cancer Centre, Ontario, Canada.
Int J Radiat Biol. 1993 Nov;64(5):593-600. doi: 10.1080/09553009314551811.
Three pairs of cell lines (one human and two Chinese hamster ovary (CHO) cell lines) each comprising a cell line with a normal radiation response and a radiation-sensitive mutant, were evaluated for recovery of potentially lethal damage (PLDR) and recovery of sublethal damage (SLDR). In all cases, the normal cell lines (GM1522, human; AA8-4 and K1, CHO) exhibited capacity for PLDR and SLDR was also normal in the two CHO lines. For the mutants (GM3395, human AT; V3 and 5-11, CHO) there was no ability for PLDR and SLDR was also absent in the two CHO cell lines. Postirradiation exposure to hypotonic NaCl solutions resulted in fixation of radiation damage in all the cell lines. This form of damage is repaired if left unperturbed after irradiation. This shows that cells have a large capacity for repair of this form of damage which accounts for much greater changes in survival than those observed in conventional PLDR experiments. These data show that the mutant cell lines retained their capacity to repair the damage which was susceptible to postirradiation fixation by anisotonic salt solutions. In addition, initial (i.e. preirradiation) DNA polymerase activities were measured in the four CHO cell lines; they were not correlated to radiation sensitivity.
评估了三对细胞系(一对人类细胞系和两对中国仓鼠卵巢(CHO)细胞系),每对均包含一个具有正常辐射反应的细胞系和一个辐射敏感突变体,以检测潜在致死损伤(PLDR)的恢复情况和亚致死损伤(SLDR)的恢复情况。在所有情况下,正常细胞系(GM1522,人类细胞系;AA8 - 4和K1,CHO细胞系)均表现出PLDR能力,并且两个CHO细胞系的SLDR也正常。对于突变体(GM3395,人类AT细胞系;V3和5 - 11,CHO细胞系),它们没有PLDR能力,并且两个CHO细胞系也不存在SLDR。照射后暴露于低渗NaCl溶液会导致所有细胞系中的辐射损伤固定。如果在照射后不进行干扰,这种形式的损伤是可以修复的。这表明细胞具有修复这种形式损伤的强大能力,这种损伤对细胞存活的影响比传统PLDR实验中观察到的要大得多。这些数据表明,突变细胞系保留了修复易受等渗盐溶液照射后固定的损伤的能力。此外,还测量了四个CHO细胞系的初始(即照射前)DNA聚合酶活性;它们与辐射敏感性无关。