Tarella C, Ferrero D, Gallo E, Pagliardi G L, Ruscetti F W
Cancer Res. 1982 Feb;42(2):445-9.
Induction of differentiation of human promyelocytic leukemia cell line HL-60 by dimethyl sulfoxide (Me2SO) was analyzed to determine the relationship between exposure time of the inducer and cell cycle. A minimum incubation time of 12 hr with Me2SO was required in order to induce differentiation in a small but significant proportion of cells. These expressed differentiation markers (morphology, phagocytosis, and nitroblue tetrazolium reduction) up to 12 hr after Me2SO was removed from the medium. For periods beyond 12 hr and as long as 120 hr of contact of HL-60 cells with the inducing agent, a linear rise in the percentage of differentiated cells was observed. The sensitivity to Me2SO of HL-60 cells synchronized by double thymidine block was examined and was found to be similar to that of nonsynchronized cells. The effect of Me2SO was not altered when incubated with cells at different phases of the cell cycle. Finally, even nonproliferating cells were sensitive to the inducing effect of Me2SO. The data are consistent with a stochastic model of induction to differentiation without having any linkage to the cell cycle.
分析了二甲基亚砜(Me2SO)对人早幼粒细胞白血病细胞系HL-60的诱导分化作用,以确定诱导剂暴露时间与细胞周期之间的关系。为了在一小部分但显著比例的细胞中诱导分化,需要用Me2SO孵育至少12小时。从培养基中去除Me2SO后长达12小时,这些细胞仍表达分化标志物(形态学、吞噬作用和硝基蓝四氮唑还原)。在HL-60细胞与诱导剂接触超过12小时且长达120小时的时间段内,观察到分化细胞百分比呈线性上升。检测了通过双胸腺嘧啶核苷阻断同步化的HL-60细胞对Me2SO的敏感性,发现其与非同步化细胞相似。当在细胞周期的不同阶段与细胞一起孵育时,Me2SO的作用没有改变。最后,即使是非增殖细胞也对Me2SO的诱导作用敏感。这些数据与诱导分化的随机模型一致,且与细胞周期没有任何关联。