Wang Nan, Wang Li-Wen, Gou Bao-Di, Zhang Tian-Lan, Wang Kui
Department of Chemical Biology, Peking University School of Pharmaceutical Sciences, 38 Xueyuan Road, Beijing 100083, PR China.
Cell Biol Int. 2008 Dec;32(12):1497-505. doi: 10.1016/j.cellbi.2008.08.017. Epub 2008 Aug 20.
The clinical efficacy and safety of realgar (arsenic sulfide, As(4)S(4)) in the treatment of acute promyelocytic leukemia in China have given rise to an upsurge in research on the underlying mechanism. We prepared realgar nanoparticles (RNPs) to examine their effect on the differentiation of HL-60 cells. Treatment with RNPs at 6 microM for 72 h induced cell differentiation that was assessed by morphological change, NBT reductive ability, and elevation of CD11b expression at both mRNA and protein levels. The RNP-induced differentiation was synergized, enhanced and suppressed by the inhibition of p38 MAPK, JNK and ERK pathways, respectively. Our findings demonstrate that MAPK signaling pathways are closely related to the RNP-induced differentiation in HL-60 cells.
在中国,雄黄(硫化砷,As(4)S(4))治疗急性早幼粒细胞白血病的临床疗效及安全性引发了对其潜在机制研究的热潮。我们制备了雄黄纳米颗粒(RNPs)以检测其对HL-60细胞分化的影响。用6 microM的RNPs处理72小时可诱导细胞分化,这通过形态学变化、NBT还原能力以及mRNA和蛋白质水平上CD11b表达的升高来评估。分别抑制p38 MAPK、JNK和ERK通路可协同、增强和抑制RNP诱导的分化。我们的研究结果表明,MAPK信号通路与RNPs诱导的HL-60细胞分化密切相关。