Schneiderman M H, Hofer K G, Schneiderman G S
Institute of Molecular Biophysics, Florida State University, Tallahassee 32306.
Int J Radiat Biol. 1991 Feb;59(2):397-408. doi: 10.1080/09553009114550361.
A radionuclide release assay for measuring the in vitro kinetics of cell death has been developed. CHO cells were labelled for 24 h with 3.0 hBq/ml of [125I] iododeoxyuridine (125IUdR) and the fate of the labelled cells and their progeny was monitored at daily intervals by measuring the rate of 125I release. Prelabelling with 125IUdR did not alter the plating efficiency, the doubling time or the selection of mitotic cells. The rate of 125I release from labelled (but otherwise untreated) CHO cells was approximately equal to 4% day. Treatment with a lethal dose of X-rays (30 Gy), heat (46 degrees C, 1 h), cold (-90 degrees C, 1 h) or the antibiotic Geneticin (300 micrograms/ml, continuously) resulted in the release of greater than 99% the 125I activity associated with the cells. Cell death was rapid after heating or freezing, and delayed after treatment with X-rays or Geneticin. The results illustrate the efficacy of the 125I release assay for measuring the kinetics of cell death in mammalian tissue culture cells.
已开发出一种用于测量细胞死亡体外动力学的放射性核素释放测定法。用3.0 hBq/ml的[125I]碘脱氧尿苷(125IUdR)对中国仓鼠卵巢(CHO)细胞标记24小时,并通过测量125I释放率,每天监测标记细胞及其子代的命运。用125IUdR进行预标记不会改变接种效率、倍增时间或有丝分裂细胞的选择。来自标记(但未作其他处理)的CHO细胞的125I释放率约为每天4%。用致死剂量的X射线(30 Gy)、热(46℃,1小时)、冷(-90℃,1小时)或抗生素遗传霉素(300微克/毫升,持续作用)处理,导致与细胞相关的125I活性释放超过99%。加热或冷冻后细胞死亡迅速,而用X射线或遗传霉素处理后细胞死亡延迟。结果说明了125I释放测定法在测量哺乳动物组织培养细胞中细胞死亡动力学方面的有效性。