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作 者:郑忠信[1] 柳约坚[1] 陈菲莉[1] 易正山[1] 董慧娟[1] 周勇[1] 周淑芸[1] 徐兵[1]
机构地区:[1]南方医科大学南方医院血液科,广东广州510515
出 处:《中山大学学报(医学科学版)》2014年第5期667-671,共5页Journal of Sun Yat-Sen University:Medical Sciences
基 金:国家自然科学基金(81070425);广东省科技计划项目(2011B031800063)
摘 要:【目的】探讨低浓度雷公藤甲素联合伊达比星(IDA)在体外对急性髓系白血病细胞(AML)干细胞凋亡的影响及其分子机制。【方法】应用流式细胞仪分选KG1a细胞中具有AML干细胞特性的CD34+CD38-亚群;对分选的CD34+CD38-KG-1α细胞进行免疫表型和细胞周期的测定;流式细胞术检测IC20浓度的雷公藤甲素、IC50浓度的IDA单药及上述浓度的雷公藤甲素联合IDA对CD34+CD38-KG1a细胞的诱导凋亡作用;蛋白质印迹法检测药物处理后HIF-1a及其下游CXCR4、VLA-4蛋白表达水平的变化。【结果】分选后CD34+CD38-亚群细胞占KG-lα细胞比例达(98.15±1.64)%,,细胞周期检测显示G0/G1期细胞比例达(82.40±3.82)%。空白对照组、IC20浓度的雷公藤甲素(5 nmol/L)单药组、IC50浓度的IDA(27nmol/L)单药组及上述浓度的雷公藤甲素联合IDA组作用于AML干细胞细胞,24 h凋亡率分别为:(5.63±0.67)%、(9.11±0.33)%、(24.85±1.70)%和(76.87±8.34)%,联合组诱导AML干细胞凋亡比较显著高于雷公藤甲素单药组及IDA单药组(均P<0.001)。蛋白质印迹法结果显示单药组及联合组均可以不同程度下调AML干细胞HIF-1a、CXCR4及VLA-4蛋白的表达水平,其中联合组最为明显。【结论】低浓度雷公藤甲素可显著提高IDA对AML干细胞诱导凋亡作用,其机制可能是通过抑制HIF-1α及其下游通路实现的。[Objective] To investigate the effect of low-dose triptolide (TRI) in combination with idarubicin (IDA) on acute myeloid leukemia stem cells and the relationship with HIF-1α pathway.[Methods] CD34^+CD38^-KG1a cells was sorted from KG1a cell lines by fluorence-activated cell sorting (FACS) analysis.Immunophenotype and cell cycle analysis of CD34^+CD38^-KG1a cells were analyzed by fluorescence-activated cell sorting analysis.Annexin-V/PI double staining was used to detect the effects of low-dose TRI in combination with IDA on apoptosis of CD34^+CD38^-KG1a cells.Western bloting to analyze the expression of HIF-1α and its downstream protein CXCR4,VLA-4 in CD34^+CD38^-KG1a cells after treatment with TRI,IDA,and TRI+IDA.[Results] After sorting,98.15-± 1.64% of the cells were labeled for CD34^+CD38^-.Cell cycle analysis also showed that proportion of G0/G1 cells was 82.4 ± 3.82%.CD34^+CD38^-KG1a cells were exposed to 5 nmol/L TPL,27 nmol/L IDA and TRI±IDA for 24 h.The apoptotic cells were determined by PI/Annexin V staining and flow cytometric analysis.Apoptotic ratio of cells treated by IDA with TPL was significantly increased compared to cells treated by IDA alone (24.85 ± 1.70% vs.76.87 ± 8.34%,P 〈 0.001).Western blot results showed markedly decrease the expression of HIF-1α,CXCR4 and VLA-4 in CD34^+CD38^-KG1a cells treated with low-dose TRI in combination with IDA.[Conclusion] A relatively low concentration of TPL in combination with IDA could induce apoptosis of AML stem cells in vitro via inhibition of HIF-1α pathway.
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