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罗哌醇四乙酸酯可降低U937细胞中细胞因子mRNA水平及转录因子的结合能力。

Rooperol tetraacetate decreases cytokine mRNA levels and binding capacity of transcription factors in U937 cells.

作者信息

Guzdek A, Rokita H, Cichy J, Allison A C, Koj A

机构信息

Institute of Molecular Biology, Jagiellonian University, Kraków, Poland.

出版信息

Mediators Inflamm. 1998;7(1):13-8. doi: 10.1080/09629359891324.

Abstract

We have previously described inhibition of the synthesis of three acute-phase inflammatory cytokines in human and rat macrophages by acetate esters of rooperol, a dicatechol of plant origin. Analysing the mechanism of anticytokine activity of rooperol, we compared levels of TNFalpha, IL-1beta and IL-6 mRNAs in the human promonocytic U937 cell line pretreated with phorbol myristate acetate (PMA) and incubated with rooperol tetraacetate (RTA) alone or in combination with LPS (500 ng/ml). It was found that 10 microM RTA decreased the levels of cytokine mRNAs both in the presence and absence of LPS, suggesting pretranslational inhibition of cytokine synthesis. Electrophoretic mobility shift analysis (EMSA) showed that RTA may influence cytokine mRNA expression by decreasing the binding activity of transcription factors NF-kappaB and AP-1.

摘要

我们之前曾描述过,源自植物的二儿茶酚罗珀醇的乙酸酯可抑制人和大鼠巨噬细胞中三种急性期炎性细胞因子的合成。在分析罗珀醇的抗细胞因子活性机制时,我们比较了用佛波酯(PMA)预处理并单独或与脂多糖(LPS,500 ng/ml)联合孵育的人原单核细胞U937细胞系中TNFα、IL-1β和IL-6 mRNA的水平。结果发现,10 μM的罗珀醇四乙酸酯(RTA)在有或没有LPS的情况下均降低了细胞因子mRNA的水平,提示对细胞因子合成的翻译前抑制。电泳迁移率变动分析(EMSA)表明,RTA可能通过降低转录因子NF-κB和AP-1的结合活性来影响细胞因子mRNA的表达。

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