Greer W L, Kaplan J G
Biochem Biophys Res Commun. 1983 Sep 30;115(3):834-40. doi: 10.1016/s0006-291x(83)80010-2.
At the onset of culture of mouse splenic lymphocytes with concanavalin A (Con A), a 6 h pulse with 5-fluorouracil (5-FU) or 8-azaguanine (8-AG), under conditions previously shown to lead to an irreversible block of the stimulated cells in the G1 phase of the cell cycle (1,2), causes extensive DNA strand breakage. Breaks induced by the analogues early in culture were largely unrepaired even after 48 h culture. Analogues that did not block the proliferative response did not cause DNA strand breakage. Unrepaired DNA strand breaks, induced by the purine and pyrimidine analogues, provide a mechanism that can account for the block of the stimulated lymphocytes before S phase. Many strand breaks were found to exist in the DNA of normal, resting splenic lymphocytes; these were rapidly repaired within 2 h of stimulation with Con A, unlike those induced by the analogues.
在用刀豆蛋白A(Con A)培养小鼠脾淋巴细胞开始时,在先前已证明会导致受刺激细胞在细胞周期G1期发生不可逆阻滞的条件下,用5-氟尿嘧啶(5-FU)或8-氮杂鸟嘌呤(8-AG)进行6小时脉冲处理,会导致广泛的DNA链断裂。培养早期由类似物诱导的断裂即使在培养48小时后也基本未修复。不阻断增殖反应的类似物不会导致DNA链断裂。嘌呤和嘧啶类似物诱导的未修复DNA链断裂提供了一种机制,可以解释受刺激淋巴细胞在S期之前的阻滞。发现正常静止脾淋巴细胞的DNA中存在许多链断裂;与类似物诱导的链断裂不同,这些链断裂在用Con A刺激后2小时内迅速修复。