Nelipovich P A, Rybalko G V, Korol' B A, Umanskiĭ S R
Biokhimiia. 1982 Oct;47(10):1663-9.
The death of rat thymocytes after irradiation or hydrocortisone injection is accompanied by degradation of DNA. DNA degradation in the thymocytes of irradiated animals starts after a 2-hr lag, reaches its maximum by the 6th hour and remains constant between the 6th and 10th hours. The accumulation of chromatin fragments after hydrocortisone injection starts without a pronounced lag period and reaches its maximum (approximately equal to 15%): by the 9th-10th hour. The amount of degraded DNA is correlated with the number of cells with psychotic nuclei. The chromatin degradation products in rat thymocytes after irradiation or hydrocortisone injection are nucleosomes and their oligomers. The number of intranucleosomal breaks in DNA is negligibly small. In vivo experiments with inhibitors of RNA and protein synthesis in the system described have demonstrated that chromatin degradation depends on protein synthesis and is almost independent of RNA synthesis. Thus, the molecular mechanisms of nuclear DNA degradation in dying thymocytes appear to be similar and independent of the nature of the agents used.
照射或注射氢化可的松后大鼠胸腺细胞的死亡伴随着DNA的降解。受照射动物胸腺细胞中的DNA降解在延迟2小时后开始,在第6小时达到最大值,并在第6至10小时保持恒定。注射氢化可的松后染色质片段的积累开始时没有明显的延迟期,并在第9至10小时达到最大值(约等于15%)。降解的DNA量与具有核固缩的细胞数量相关。照射或注射氢化可的松后大鼠胸腺细胞中的染色质降解产物是核小体及其寡聚体。DNA中核小体内断裂的数量极少。在所描述的系统中使用RNA和蛋白质合成抑制剂进行的体内实验表明,染色质降解依赖于蛋白质合成,几乎与RNA合成无关。因此,垂死胸腺细胞中核DNA降解的分子机制似乎相似,且与所用试剂的性质无关。