首页> 外文期刊>Leukemia Research and Treatment >Cell-Type-Specific Effects of Silibinin on Vitamin D-Induced Differentiation of Acute Myeloid Leukemia Cells Are Associated with Differential Modulation of RXRαLevels
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Cell-Type-Specific Effects of Silibinin on Vitamin D-Induced Differentiation of Acute Myeloid Leukemia Cells Are Associated with Differential Modulation of RXRαLevels

机译:水飞蓟宾对维生素D诱导的急性髓性白血病细胞分化的细胞类型特异性作用与RXRα水平的差异调节有关。

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Plant polyphenols have been shown to enhance the differentiation of acute myeloid leukemia (AML) cells induced by the hormonal form of vitamin D3(1α,25-dihydroxyvitamin D3; 1,25D). However, how these agents modulate 1,25D effects in different subtypes of AML cells remains poorly understood. Here, we show that both carnosic acid (CA) and silibinin (SIL) synergistically enhancd 1,25D-induced differentiation of myeloblastic HL60 cells. However, in promonocytic U937 cells, only CA caused potentiation while SIL attenuated 1,25D effect. The enhanced effect of 1,25D+CA was accompanied by increases in both the vitamin D receptor (VDR) and retinoid X receptor alpha (RXRα) protein levels and vitamin D response element (VDRE) transactivation in both cell lines. Similar increases were observed in HL60 cells treated with 1,25D + SIL. In U937 cells, however, SIL inhibited 1,25D-induced VDRE transactivation concomitant with downregulation of RXRαat both transcriptional and posttranscriptional levels. These inhibitory effects correlated with the inability of SIL, with or without 1,25D, to activate the Nrf2/antioxidant response element signaling pathway in U937 cells. These results suggest that opposite effects of SIL on 1,25D-induced differentiation of HL60 and U937 cells may be determined by cell-type-specific signaling and transcriptional responses to this polyphenol resulting in differential modulation of RXRαexpression.
机译:已显示植物多酚可增强激素形式的维生素D3(1α,25-二羟基维生素D3; 1,25D)诱导的急性髓样白血病(AML)细胞分化。但是,这些药物如何调节AML细胞不同亚型的1,25D效果仍知之甚少。在这里,我们表明肌酸(CA)和水飞蓟宾(SIL)协同增强了1,25D诱导的骨髓小细胞HL60细胞的分化。但是,在原核单核细胞U937细胞中,只有CA会引起增强作用,而SIL会减弱1,25D效应。 1,25D + CA的增强作用伴随着两种细胞系中维生素D受体(VDR)和类维生素X受体α(RXRα)蛋白质水平以及维生素D反应元件(VDRE)反式激活的增加。在用1,25D + SIL处理的HL60细胞中观察到类似的增加。然而,在U937细胞中,SIL抑制了1,25D诱导的VDRE反式激活,同时在转录和转录后水平上均抑制了RXRα。这些抑制作用与有或无1,25D的SIL不能激活U937细胞中的Nrf2 /抗氧化反应元件信号通路有关。这些结果表明,SIL对1,25D诱导的HL60和U937细胞分化的相反作用可以通过细胞类型特异性信号传导和对该多酚的转录反应来确定,从而导致RXRα表达的差异调节。

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