Schneiderman M H, Schneiderman G S, Rusk C M
Cell Tissue Kinet. 1983 Jan;16(1):41-9.
G2 cells treated with 150 rad X-radiation were isolated from a monolayer culture of exponentially growing Chinese hamster ovary (CHO) cells by a combination of 125Iododeoxyuridine ([125I]UdR)-induced blockade of S-phase cell progression, treatment and mitotic selection (125I-TMS technique). Once the rate at which cells were selected from a small window in mitosis was established (Schneiderman et al., 1972), the cells were exposed to 10 microCi/ml, carrier-free [125I]UdR for 10 min immediately before treatment with 150 rads X-radiation. After X-irradiation the cells located later in the cell cycle than the X-ray-induced division delay transition point (TPx), at or just prior to prophase, progressed without delay and were selected during the next 50 min (Walters & Petersen, 1968; Schneiderman et al., 1972). The G2- and S-phase cells, located prior to the TPx, sustained a transitory delay and resumed progression into mitosis only after recovery from the radiation insult (Terasima & Tolmach, 1963). However, S-phase cells having incorporated [125I]UdR during the pulse label were prevented from entering mitosis (Schneiderman & Hofer, 1980) and only the X-ray-treated G2 cells resumed progression into mitosis and were selected.
通过¹²⁵碘脱氧尿苷([¹²⁵I]UdR)诱导的S期细胞进程阻断、处理和有丝分裂选择(¹²⁵I-TMS技术)的组合,从指数生长的中国仓鼠卵巢(CHO)细胞的单层培养物中分离出经150拉德X射线辐射处理的G2期细胞。一旦确定了从有丝分裂的一个小窗口中选择细胞的速率(施奈德曼等人,1972年),就在用150拉德X射线辐射处理前10分钟,将细胞暴露于10微居里/毫升、无载体的[¹²⁵I]UdR中10分钟。X射线照射后,位于细胞周期中比X射线诱导的分裂延迟转变点(TPx)更靠后的细胞,即在前期或刚好在前期之前的细胞,无延迟地进行分裂,并在接下来的50分钟内被选择(沃尔特斯和彼得森,1968年;施奈德曼等人,1972年)。位于TPx之前的G2期和S期细胞经历了短暂的延迟,只有在从辐射损伤中恢复后才恢复进入有丝分裂的进程(寺岛和托尔马赫,1963年)。然而,在脉冲标记期间掺入了[¹²⁵I]UdR的S期细胞被阻止进入有丝分裂(施奈德曼和霍费尔,1980年),只有经X射线处理的G2期细胞恢复进入有丝分裂并被选择。