狼毒大戟中二萜类化合物DP抗白血病的作用机制研究
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篇名: 狼毒大戟中二萜类化合物DP抗白血病的作用机制研究
TITLE: Study on the mechanism of diterpenoid DP from Euphorbia fischeriana against leukemia
摘要: 目的 探究狼毒大戟中二萜类化合物12-去氧佛波醇-13-棕榈酸酯(DP)能否通过磷脂酰肌醇3激酶(PI3K)/蛋白激酶B(Akt)信号通路发挥抗白血病的作用,为将其开发成抗白血病新药提供实验依据。方法以LY294002(PI3K特异性抑制剂)为工具药,采用MTT、AnnexinⅤ-FITC/PI、AO-EB染色法观察并测定DP作用24h后对人原髓细胞白血病细胞HL60增殖、凋亡的影响;采用ELISA法测定DP作用24h后细胞培养液中乳酸脱氢酶(LDH)的释放量及细胞中胱天蛋白酶3(caspase-3)、caspase-9的活性。采用实时荧光定量-PCR法检测DP作用24h后细胞中caspase-3、caspase-9、叉头框O3a(FoxO3a)、B细胞淋巴瘤2细胞死亡的相互作用介质(Bim)的mRNA转录水平;采用Westernblot法检测细胞中磷酸化FoxO3a(p-FoxO3a)、磷酸化Akt(p-Akt)的蛋白表达水平,并采用免疫染色法在激光共聚焦显微镜下观察细胞中FoxO3a蛋白核转位情况。结果10μmol/LDP和10μmol/LDP+LY294002对HL60细胞有明显的增殖抑制及凋亡诱导作用(P<0.01);5、10、20μmol/LDP作用后的细胞均呈典型的凋亡形态学特征,细胞培养液中LDH释放量和细胞中caspase-3、caspase-9活性均显著升高(P<0.05或P<0.01),其作用具有一定的浓度依赖性趋势;10μmol/LDP和10μmol/LDP+LY294002作用后细胞中caspase-3、caspase-9和BimmRNA转录水平均显著升高(P<0.05或P<0.01),FoxO3amRNA转录水平和p-FoxO3a、p-Akt蛋白表达水平均显著降低(P<0.05或P<0.01);10μmol/LDP+LY294002组细胞可见FoxO3a蛋白的核转位变化,且该变化较LY294002组明显。结论DP可通过抑制PI3K/Akt信号通路抑制人白血病HL60细胞增殖并诱导其凋亡。
ABSTRACT: OBJECTIVE To explore whether diterpenoid 12-deoxyphorbol-13-palmitate (DP) from Euphorbia fischeriana can exert anti-leukemia effects through the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (Akt) signal pathway, and to provide experimental evidence for developing it into a new anti-leukemia drug. METHODS Using LY294002 (PI3K specific inhibitor) as tool drug, the effects of 24 h DP treatment on the proliferation and apoptosis of human myeloid leukemia HL60 cells were detected by MTT method, Annexin Ⅴ-FITC/PI staining and AO-EB staining. ELISA method was used to detect lactic dehydrogenase (LDH) release and the activities of cysteinyl aspartate specific proteinase 3 (caspase-3) and caspase-9. The transcriptional level of caspase-3, caspase-9, forkhead box O3a (FoxO3a) and B cell lymphoma 2 interacting mediator of cell death (Bim) mRNA were detected by real-time quantitative polymerase chain reaction (qRT-PCR). The protein expression of phosphorylated FoxO3a (p- FoxO3a) and phosphorylated Akt (p-Akt) were detected by Western blot method. The nuclear translocation of FoxO3a protein was detected by immunostaining combined with laser confocal microscopy. RESULTS 10 μmol/L DP and 10 μmol/L DP+LY294002 could inhibit the proliferation and induce the apoptosis of HL60 cells (P<0.01). After treatment of 5, 10, 20 μmol/L DP, HL60 cells showed typical morphological characteristics of apoptosis; DP could significantly increase the levels of LDH release and the activities of caspase-3 and caspase-9 (P<0.05 or P<0.01), in dose-dependent manner. After treatment of 10 μmol/L DP and 10 μmol/L DP+LY294002, the transcriptional levels of caspase-3, caspase-9 and Bim mRNA were increased significantly (P<0.05 or P<0.01), and transcriptional level of FoxO3a mRNA and protein expressions of p-FoxO3a and p-Akt were decreased significantly (P<0.05 or P<0.01). Nuclear translocation changes were observed in FoxO3a protein in 10 μmol/L DP+LY294002 group, and the change was more significant than that of LY294002 group. CONCLUSIONS DP can inhibit the proliferation and induce the apoptosis of HL60 cells via inhibiting PI3K/Akt signaling pathway.
期刊: 2023年第34卷第07期
作者: 马立威;陈哲;王文豹;张金玲;张洪涛;葛鹏玲;刘吉成
AUTHORS: MA Liwei,CHEN Zhe,WANG Wenbao,ZHANG Jinling,ZHANG Hongtao,GE Pengling,LIU Jicheng
关键字: 狼毒大戟;12-去氧佛波醇-13-棕榈酸酯;人原髓细胞白血病细胞HL60;磷脂酰肌醇3激酶/蛋白激酶B信号通路
KEYWORDS: Euphorbia fischeriana; 12-deoxyphorbol-13-palmitate; human myeloid leukemia HL60 cells; phosphoinositide 3-
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