Pulito V L, Miller D L, Sassa S, Yamane T
J Biol Chem. 1983 Dec 25;258(24):14756-8.
A variety of chemical agents that are known to induce erythrodifferentiation in the Friend virus-induced murine erythroleukemia (MEL) cell have been suggested to mediate DNA cleavage in cultured cells prior to differentiation. The activation of the nuclear enzyme, ADP-ribosyltransferase, depends upon the presence of single strand breaks in DNA. If dimethyl sulfoxide (Me2SO) causes DNA breakage, it would be expected that the activity of ADP-ribosyltransferase would increase. A study of ADP-ribosyltransferase activity during cell growth indicates that both Me2SO-treated and untreated MEL cells exhibit a similar increase in the enzyme activity but the increase in Me2SO-treated cells is delayed by a few hours. When examined at comparable stages of growth, both treated and untreated cells show almost identical levels of enzyme activity. The present data thus do not support the contention that Me2SO induces DNA breakage in the MEL cells.
已知多种能在弗氏病毒诱导的小鼠红白血病(MEL)细胞中诱导红系分化的化学试剂,被认为在分化前介导培养细胞中的DNA切割。核酶ADP-核糖基转移酶的激活取决于DNA中单链断裂的存在。如果二甲基亚砜(Me2SO)导致DNA断裂,那么预计ADP-核糖基转移酶的活性会增加。一项关于细胞生长过程中ADP-核糖基转移酶活性的研究表明,经Me2SO处理和未处理的MEL细胞中该酶活性均有类似增加,但经Me2SO处理的细胞中活性增加会延迟数小时。在生长的可比阶段进行检测时,处理组和未处理组细胞显示出几乎相同的酶活性水平。因此,目前的数据不支持二甲基亚砜在MEL细胞中诱导DNA断裂这一论点。