Becker R W, Tyobeka E M
Department of Biochemistry, University of the North, Sovenga, South Africa.
Leuk Res. 1992 Aug;16(8):823-8. doi: 10.1016/0145-2126(92)90162-z.
The human promyelocytic leukemia cell line, HL-60, was used to investigate the effects of lithium on dimethyl sulfoxide (DMSO)-induced granulocytic differentiation of these cells. Dose-response studies showed an optimal increase of cellular proliferation when cells were incubated with 5 mM lithium for 5 days (127 +/- 5% of DMSO only treated cells). This enhancement in growth was preceded by significantly increased [methyl-3H]thymidine incorporation (143 +/- 4% of DMSO only treated controls) after 2 days. However, no significant changes in the ability of cells to reduce NBT could be detected irrespective of whether the cells were incubated with 1.25% (v/v) DMSO only, or with DMSO plus non-toxic concentrations (less than or equal to 10 mM) lithium. From the results obtained it would appear as if the arrest of growth induced by DMSO and the stimulation of proliferation effected by lithium occurs along independent pathways and that lithium exerts its mitogenic effect prior to the onset of terminal differentiation initiated by DMSO.
人类早幼粒细胞白血病细胞系HL-60被用于研究锂对二甲基亚砜(DMSO)诱导的这些细胞粒细胞分化的影响。剂量反应研究表明,当细胞与5 mM锂孵育5天时,细胞增殖有最佳增加(仅用DMSO处理的细胞的127±5%)。在这种生长增强之前,2天后[甲基-3H]胸苷掺入显著增加(仅用DMSO处理的对照的143±4%)。然而,无论细胞是仅与1.25%(v/v)DMSO孵育,还是与DMSO加无毒浓度(小于或等于10 mM)锂孵育,都未检测到细胞还原NBT能力的显著变化。从获得的结果来看,似乎DMSO诱导的生长停滞和锂引起的增殖刺激是沿着独立的途径发生的,并且锂在DMSO引发的终末分化开始之前发挥其促有丝分裂作用。