Qian Xi-Jun, Lin Mao-Fang
Department of Hematology, First Affiliated Hospital, Medical College of Zhejiang University, Hangzhou 310003, China.
Zhonghua Xue Ye Xue Za Zhi. 2006 Jul;27(7):445-8.
To investigate the effect of aminopeptidase N inhibitor ubenimex on differentiation induction of all-trans-retinoic acid (ATRA) in acute promyelocytic leukemia (APL) cells and its mechanism.
The expression of CD11b was analyzed by flow cytometry and nitroblue-tetrazolium (NBT) reduction assay was performed to determine the cell differentiation of APL cells. The expressions of c-Myc, ERK1/2, p38MAPK protein and the phosphorylation of ERK1/2, p38MAPK protein in NB4 cells were detected by Western blot assay.
Ubenimex alone induced no significant changes in NBT reduction activity and CD11b expression but potentiated the differentiation induction activity of ATRA in APL cells. 100 microg/ml of ubenimex could enhance the NBT reduction activity induced by 10 nmol/L of ATRA, intensify the down-regulation of c-Myc protein expression and inhibit the phosphorylation of p38MAPK protein induced by 10 nmol/L of ATRA in NB4 cells.
Ubenimex could potentiate ATRA induced differentiation in APL cells, which may be correlated with the inhibition of p38 MAPK protein phosphorylation and regulation of c-Myc protein expression.
探讨氨肽酶N抑制剂乌苯美司对急性早幼粒细胞白血病(APL)细胞全反式维甲酸(ATRA)诱导分化的影响及其机制。
采用流式细胞术分析CD11b的表达,并进行硝基蓝四氮唑(NBT)还原试验以确定APL细胞的分化情况。通过蛋白质免疫印迹法检测NB4细胞中c-Myc、ERK1/2、p38MAPK蛋白的表达以及ERK1/2、p38MAPK蛋白的磷酸化水平。
单独使用乌苯美司对NBT还原活性和CD11b表达无显著影响,但可增强ATRA对APL细胞的分化诱导活性。100μg/ml的乌苯美司可增强10nmol/L ATRA诱导的NBT还原活性,强化c-Myc蛋白表达的下调,并抑制10nmol/L ATRA诱导的NB4细胞中p38MAPK蛋白的磷酸化。
乌苯美司可增强ATRA对APL细胞的诱导分化作用,这可能与抑制p38 MAPK蛋白磷酸化及调节c-Myc蛋白表达有关。