Kaplinsky C, Estrov Z, Freedman M H, Gelfand E W, Cohen A
Division of Immunology/Rheumatology, Hospital for Sick Children, Toronto, Ontario, Canada.
Leukemia. 1987 May;1(5):437-41.
The ribonucleotide reductase inhibitors deferoxamine and hydroxyurea induce monocyte-macrophage cell differentiation in the leukemic cell line HL-60 as judged by the expression of cell surface antigens, nonspecific esterase activity, and morphological changes. Treatment of HL-60 cells with deferoxamine results in inhibition of DNA synthesis and irreversible loss of colony-forming ability. In addition, both deferoxamine and hydroxyurea caused an increase in the number of DNA strand breaks in HL-60 cells. A DNA methylating agent, N-methyl-N'-nitro-N-nitrosoguanidine, also caused cellular differentiation in HL-60 cells associated with DNA strand breaks. These observations are consistent with a role for DNA damage or for inhibition of DNA synthesis and repair in the differentiation process of HL-60 cells.
通过细胞表面抗原的表达、非特异性酯酶活性和形态学变化判断,核糖核苷酸还原酶抑制剂去铁胺和羟基脲可诱导白血病细胞系HL-60中的单核细胞-巨噬细胞分化。用去铁胺处理HL-60细胞会导致DNA合成受到抑制以及集落形成能力的不可逆丧失。此外,去铁胺和羟基脲均导致HL-60细胞中DNA链断裂数量增加。一种DNA甲基化剂N-甲基-N'-硝基-N-亚硝基胍也可导致与DNA链断裂相关的HL-60细胞分化。这些观察结果与DNA损伤或DNA合成及修复抑制在HL-60细胞分化过程中的作用一致。