Miyoshi Y, Nakamura H, Tagami T, Sasaki S, Nakao K
Department of Internal Medicine, Kyoto University School of Medicine, Japan.
Mol Cell Endocrinol. 1994 Jul;103(1-2):119-23. doi: 10.1016/0303-7207(94)90078-7.
The human acute promyelocytic leukemia (APL) cell line HL-60 differentiates to functionally mature granulocytes by incubation with all-trans-retinoic acid (RA). Since T3 and RA are important in cell differentiation and development, and since their receptors are highly homological, we investigated the T3 effects on RA-induced HL-60 cell differentiation. Although T3 alone did not induce cell differentiation, RA-mediated differentiation was significantly enhanced in the presence of 10(-7) M T3. This effect of T3 was considered to be mediated, at least in part, by increased intracellular cAMP, since the phosphodiesterase inhibitor enhanced, and the protein kinase A antagonist partially blocked, T3 potentiation. When HL-60 cells were pretreated with RA for 20 h, T3 alone stimulated the cell differentiation. The time-course study showed that incubation with RA for 12 h was necessary for HL-60 cells to be primed to respond to T3 for differentiation. The present finding that T3 potentiates RA-induced HL-60 cell differentiation may raise the possibility that T3 supplement increases clinical remission in APL patients who are treated with RA.
人急性早幼粒细胞白血病(APL)细胞系HL - 60通过与全反式维甲酸(RA)孵育可分化为功能成熟的粒细胞。由于T3和RA在细胞分化和发育中起重要作用,且它们的受体高度同源,我们研究了T3对RA诱导的HL - 60细胞分化的影响。尽管单独的T3不诱导细胞分化,但在10(-7)M T3存在下,RA介导的分化显著增强。T3的这种作用至少部分被认为是由细胞内cAMP增加介导的,因为磷酸二酯酶抑制剂增强了T3的增强作用,而蛋白激酶A拮抗剂部分阻断了T3的增强作用。当HL - 60细胞用RA预处理20小时后,单独的T3刺激细胞分化。时间进程研究表明,HL - 60细胞需要用RA孵育12小时才能被启动以响应T3进行分化。目前T3增强RA诱导的HL - 60细胞分化的发现可能增加了T3补充剂可提高接受RA治疗的APL患者临床缓解率的可能性。