Matylevich N P, Korol' B A, Nelipovich P A, Afanas'ev V N, Umanskiĭ S R
Radiobiologiia. 1991 Jan-Feb;31(1):27-32.
Using the method of flow cytometry and biochemical analysis it was shown that D2O, an agent that stabilizes microtubules, prevented the internucleosome fragmentation of DNA in thymocytes exposed to gamma radiation and dexamethasone in vitro. It was also found that D2O is ineffective with respect to Ca2+/Mg2(+)-dependent nuclease. The transfer of irradiated cells from a medium containing 90% of D2O to a normal one caused rapid DNA degradation; the fragmentation process ceased with the irradiated cells being transferred from H2O to heavy water. The results obtained permit us to assume that the disturbance of microtubules is not a trigger mechanism of DNA degradation by apoptosis, but is some intermediate stage of cell death preceding the chromatin fragmentation proper.
运用流式细胞术和生化分析方法表明,D2O(一种能稳定微管的试剂)可防止体外暴露于γ射线和地塞米松的胸腺细胞中DNA的核小体间断裂。还发现D2O对Ca2+/Mg(+)-依赖性核酸酶无效。将辐照后的细胞从含90% D2O的培养基转移至正常培养基会导致DNA迅速降解;当辐照后的细胞从H2O转移至重水时,断裂过程停止。所得结果使我们能够假定,微管紊乱并非细胞凋亡导致DNA降解的触发机制,而是细胞死亡在染色质真正断裂之前的某个中间阶段。