首页> 外文期刊>Anti-cancer drugs >Betulinic acid enhances 1alpha,25-dihydroxyvitamin D3-induced differentiation in human HL-60 promyelocytic leukemia cells.
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Betulinic acid enhances 1alpha,25-dihydroxyvitamin D3-induced differentiation in human HL-60 promyelocytic leukemia cells.

机译:桦木酸增强人HL-60早幼粒细胞白血病细胞中1alpha,25-dihydroxyvitamin D3诱导的分化。

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摘要

Betulinic acid (BA) is a pentacyclic triterpene found in a number of medicinal plants and has been shown to cause apoptosis in a number of cell lines. We report here that BA may also have an effect on HL-60 cell differentiation. BA was cytotoxic to HL-60 cells with an IC50 of 5.7 microM after a 72-h treatment. Flow cytometry analysis showed that after exposure to 1-12 microM of BA for 72 h, approximately 10% of viable cells were in the sub-G1, presumably apoptotic, phase. At the same time differentiation was induced in approximately 10% (at 1 microM BA) to a maximum of 20% (at 6 microM BA) of cells as judged by the NBT-reduction test, and the expression of membrane markers CD11b and CD14. On the other hand, at 1 and 5 nM, 1alpha,25-dihydroxyvitamin D3 (DHD3) induced differentiation in approximately 10 and 70% of cells, respectively. At 1 nM DHD3, the addition of 1 microM BA increased differentiated cells from 10 to 43% and with 3 microM BA the increase was to 80%. BA also enhanced the effects of DHD3 in the expansion of the G1 cell population with a concomitant decrease of S phase cells. The effects of DHD3 and BA on CD11b and CD14 expression were inhibited by PD98059, a MEK inhibitor. Our results suggest that BA may enhance the effect of DHD3 in inducing mitogen-activated protein kinase kinase/extracellular signal-regulated protein kinase-mediated HL-60 cell differentiation.
机译:桦木酸(BA)是在许多药用植物中发现的五环三萜,并且已显示其在许多细胞系中引起凋亡。我们在这里报告BA可能也对HL-60细胞分化产生影响。处理72小时后,BA对HL-60细胞具有细胞毒性,IC50为5.7 microM。流式细胞仪分析显示,暴露于1-12 microM BA 72小时后,大约10%的活细胞处于亚G1期,可能是凋亡期。同时,通过NBT还原测试以及膜标记CD11b和CD14的表达,可以诱导大约10%(1 microM BA)分化为最大20%(6 microM BA)的细胞。另一方面,在1和5 nM下,1α,25-二羟基维生素D3(DHD3)分别诱导了大约10%和70%的细胞分化。在1 nM DHD3下,添加1 microM BA可使分化的细胞从10%增加至43%,添加3 microM BA则使分化细胞增加至80%。 BA还增强了DHD3在G1细胞群体扩展中的作用,同时减少了S期细胞。 MEK抑制剂PD98059抑制DHD3和BA对CD11b和CD14表达的影响。我们的结果表明,BA可能增强DHD3诱导丝裂原活化的蛋白激酶激酶/细胞外信号调节的蛋白激酶介导的HL-60细胞分化的作用。

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