Tidwell T, Guzman G, Vogler W R
Blood. 1981 Apr;57(4):794-7.
The action of an alkyl-lysophospholipid (ALP), ET180CH3, on clonogenicity, 3H-TdR uptake, and cell numbers was tested in two human leukemic cell lines, HL60 and K562, and short-term human leukemic bone marrow cultures. ALP eliminated clonogenicity in HL60 but not in K562 cultures; 3H-TdR uptake and cell numbers were depressed at low concentrations of ET180CH3 in HL60, but not K562 cultures. The action of the lysophospholipid analog on human leukemic bone marrow short-term cultures at low concentrations was similar to its action on HL60 cultures; clonogenicity and 3H-TdR uptake were depressed, but cell numbers were not significantly affected. The demonstration of differential action of ALP on two cell lines should significantly simplify the investigation of the mechanism of the reported differential action of ET180CH3 on normal and leukemic cell membranes.
在两种人类白血病细胞系HL60和K562以及短期人类白血病骨髓培养物中,测试了烷基溶血磷脂(ALP)ET180CH3对克隆形成能力、3H-胸腺嘧啶核苷摄取和细胞数量的作用。ALP消除了HL60中的克隆形成能力,但在K562培养物中未消除;在HL60中,低浓度的ET180CH3会抑制3H-胸腺嘧啶核苷摄取和细胞数量,但在K562培养物中则不会。溶血磷脂类似物在低浓度下对人类白血病骨髓短期培养物的作用与其对HL60培养物的作用相似;克隆形成能力和3H-胸腺嘧啶核苷摄取受到抑制,但细胞数量未受到显著影响。ALP对两种细胞系的差异作用的证明应能显著简化对ET180CH3对正常和白血病细胞膜的报道差异作用机制的研究。