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(-)-表没食子儿茶素没食子酸酯抑制小鼠树突状细胞中吲哚胺2,3-双加氧酶的表达:环氧化酶-2和信号转导和转录激活因子1作为潜在靶点的证据

(-)-Epigallocatechin gallate suppresses indoleamine 2,3-dioxygenase expression in murine dendritic cells: evidences for the COX-2 and STAT1 as potential targets.

作者信息

Jeong Young-Il, Jung In Duk, Lee Jun Sik, Lee Chang-Min, Lee Jae-Dong, Park Yeong-Min

机构信息

Department of Microbiology, Pusan National University College of Natural Science, Busan, Republic of Korea.

出版信息

Biochem Biophys Res Commun. 2007 Mar 23;354(4):1004-9. doi: 10.1016/j.bbrc.2007.01.076. Epub 2007 Jan 23.

Abstract

(-)-Epigallocatechin gallate (EGCG), a major form of tea catechin, is suggested to exhibit antioxidant and anticyclooxygenase properties. Indoleamine 2,3-dioxygenase (IDO), as a key enzyme in T cell suppression and induction of immune tolerance to tumor, is expressed in various cell types. In the present study, we investigated whether EGCG could suppress the expression of IDO in murine bone marrow-derived dendritic cells (BMDCs) stimulated with IFN-gamma. We obtained evidence that EGCG suppresses the expression and activity of IDO and significantly recovers the IDO-dependent T cell suppression. To determine whether these inhibitory effect of EGCG is associated with the alteration of the signal transducer and activator of transcription 1 (STAT1) and interferon regulatory factor 1 (IRF-1) as well as COX-2 expression, BMDCs were pretreated with various concentrations of EGCG. We found that EGCG inhibited the activation and binding of STAT1 to the IRF-1 promoter in response to IFN-gamma. Furthermore, EGCG inhibited the expression of COX-2 and the production of PGE(2). Based on our results, this study may account that EGCG could inhibit IDO expression by down-regulation of STAT1 activation and COX-2 expression in IFN-gamma-stimulated murine DCs.

摘要

(-)-表没食子儿茶素没食子酸酯(EGCG)是茶儿茶素的主要形式,被认为具有抗氧化和抗环氧化酶特性。吲哚胺2,3-双加氧酶(IDO)作为T细胞抑制和诱导肿瘤免疫耐受的关键酶,在多种细胞类型中表达。在本研究中,我们调查了EGCG是否能抑制用γ干扰素刺激的小鼠骨髓来源树突状细胞(BMDC)中IDO的表达。我们获得的证据表明,EGCG抑制IDO的表达和活性,并显著恢复IDO依赖的T细胞抑制。为了确定EGCG的这些抑制作用是否与信号转导和转录激活因子1(STAT1)、干扰素调节因子1(IRF-1)的改变以及COX-2表达有关,用不同浓度的EGCG预处理BMDC。我们发现,EGCG抑制了STAT1对γ干扰素的反应而与IRF-1启动子的激活和结合。此外,EGCG抑制COX-2的表达和PGE2的产生。基于我们的结果,本研究可能认为EGCG可通过下调γ干扰素刺激的小鼠树突状细胞中STAT1的激活和COX-2的表达来抑制IDO的表达。

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