Szabo E, Francis J, Birrer M J
Medicine Branch, Division of Clinical Sciences, National Cancer Institute, 9610 Medical Center Drive, Room 300, Rockville, MD 20850, USA.
Int J Oncol. 1998 Feb;12(2):403-9. doi: 10.3892/ijo.12.2.403.
Recent evidence suggests that c-jun plays a pivotal role in macrophage differentiation induced by multiple agents and that cJun overexpression induces partial macrophage differentiation in the leukemic cell line U-937. The novel differentiating agent bufalin, a Na+/K+ ATPase inhibitor, has also been shown to induce macrophage differentiation in U-937. In order to further define the role of c-jun in macrophage differentiation, we examined the function of c-jun/AP-1 during bufalin induced differentiation in both c-jun transfected and parental U-937 cells. In contrast to phorbol esters, bufalin does not significantly stimulate c-jun or c-fos mRNA expression or AP-1 transactivation. However, bufalin treatment leads to markedly greater morphologic and functional changes indicative of more extensive differentiation in the cJun overexpressing cells compared to the non-transfected controls. Furthermore, cJun overexpressing cells maintain greater viability in the presence of bufalin and arrest in a different phase of the cell cycle than do control cell lines (G0/G1 versus S/G2M, respectively), although some apoptosis occurs in all cell lines treated with bufalin. These data suggest that while bufalin can induce some degree of differentiation in U-937 cells independent of c-jun/AP-1 controlled pathways, the involvement of these pathways by enforced cJun expression enhances the extent of differentiation and shifts the balance between differentiation and apoptosis.
近期证据表明,c-jun在多种因子诱导的巨噬细胞分化过程中起关键作用,且cJun过表达可诱导白血病细胞系U-937发生部分巨噬细胞分化。新型分化剂蟾毒灵是一种Na+/K+ ATP酶抑制剂,也已被证明可诱导U-937细胞发生巨噬细胞分化。为了进一步明确c-jun在巨噬细胞分化中的作用,我们检测了c-jun/AP-1在蟾毒灵诱导c-jun转染的U-937细胞和亲本U-937细胞分化过程中的功能。与佛波酯不同,蟾毒灵不会显著刺激c-jun或c-fos mRNA表达或AP-1反式激活。然而,与未转染的对照相比,蟾毒灵处理导致cJun过表达细胞出现更明显的形态和功能变化,表明其分化程度更高。此外,在蟾毒灵存在的情况下,cJun过表达细胞保持更高的活力,且与对照细胞系相比,其细胞周期停滞于不同阶段(分别为G0/G1期和S/G2M期),尽管在用蟾毒灵处理的所有细胞系中均有一些细胞发生凋亡。这些数据表明,虽然蟾毒灵可在U-937细胞中诱导一定程度的分化,且不依赖于c-jun/AP-1控制的途径,但通过强制表达cJun使这些途径的参与可增强分化程度,并改变分化与凋亡之间的平衡。