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首页> 外文期刊>International immunopharmacology >Penta-O-galloyl-beta-D-glucose inhibits phorbol myristate acetate-induced intereukin-8 gene expression in human monocytic U937 cells through its inactivation of nuclear factor-kappaB.
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Penta-O-galloyl-beta-D-glucose inhibits phorbol myristate acetate-induced intereukin-8 gene expression in human monocytic U937 cells through its inactivation of nuclear factor-kappaB.

机译:Penta-O-galloyl-β-D-葡萄糖通过其核因子-κB的失活抑制人单核细胞U937细胞中佛豆蔻肉豆蔻酸酯乙酸盐诱导的intereukin-8基因表达。

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摘要

We investigated the effects of the gallotannin penta-O-galloyl-beta-d-glucose (PGG) on interleukin (IL)-8 gene expression and nuclear factor (NF)-kappaB activation. PGG inhibited IL-8 production and gene expression in human monocytic U937 cells stimulated with phorbol myristate acetate (PMA), as measured by enzyme-linked immunosorbent assay and reverse transcription-polymerase chain reaction analysis, respectively. PGG also inhibited PMA-mediated NF-kappaB activation, as measured by electromobility shift assay. Furthermore, PGG prevented PMA-mediated degradation of the NF-kappaB inhibitory protein I-kappaBalpha, as measured by Western blot analysis. PGG also inhibited both IL-8 production and NF-kappaB activation in the U937 cells stimulated with tumor necrosis factor-alpha. These results suggest that PGG, a major constituent of the root cortex of Paeonia suffruticosa ANDREWS, can inhibit IL-8 gene expression by a mechanism involving its inhibition of NF-kappaB activation, which is dependent on I-kappaBalpha degradation.
机译:我们调查了gallotannin五-O-galloyl-β-d-葡萄糖(PGG)对白介素(IL)-8基因表达和核因子(NF)-kappaB激活的影响。如分别通过酶联免疫吸附测定和逆转录-聚合酶链反应分析所测量,PGG抑制了佛波肉豆蔻酸酯乙酸酯(PMA)刺激的人单核U937细胞中IL-8的产生和基因表达。如通过电动迁移率测定法所测量,PGG还抑制PMA介导的NF-κB活化。此外,如通过蛋白质印迹分析所测量的,PGG阻止了PMA介导的NF-κB抑制蛋白I-κBalpha的降解。 PGG还抑制了肿瘤坏死因子-α刺激的U937细胞中IL-8的产生和NF-κB的激活。这些结果表明,PGG是白Pa药ANDREWS的根皮层的主要成分,可以通过涉及其抑制NF-κB活化的机制来抑制IL-8基因表达,所述机制依赖于I-κB降解。

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