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姜黄素通过阻断钙动员和激活 T 细胞核因子(NFAT)的激活来抑制 T 细胞的激活。

Curcumin suppresses T cell activation by blocking Ca2+ mobilization and nuclear factor of activated T cells (NFAT) activation.

机构信息

Technologietransfer (T010), German Cancer Research Center (DKFZ), D-69120 Heidelberg, Germany.

Tumorimmunology Program (D030), German Cancer Research Center (DKFZ), D-69120 Heidelberg, Germany.

出版信息

J Biol Chem. 2012 Mar 23;287(13):10200-10209. doi: 10.1074/jbc.M111.318733. Epub 2012 Feb 2.

Abstract

Curcumin is the active ingredient of the spice turmeric and has been shown to have a number of pharmacologic and therapeutic activities including antioxidant, anti-microbial, anti-inflammatory, and anti-carcinogenic properties. The anti-inflammatory effects of curcumin have primarily been attributed to its inhibitory effect on NF-κB activity due to redox regulation. In this study, we show that curcumin is an immunosuppressive phytochemical that blocks T cell-activation-induced Ca(2+) mobilization with IC(50) = ∼12.5 μM and thereby prevents NFAT activation and NFAT-regulated cytokine expression. This finding provides a new mechanism for curcumin-mediated anti-inflammatory and immunosuppressive function. We also show that curcumin can synergize with CsA to enhance immunosuppressive activity because of different inhibitory mechanisms. Furthermore, because Ca(2+) is also the secondary messenger crucial for the TCR-induced NF-κB signaling pathway, our finding also provides another mechanism by which curcumin suppresses NF-κB activation.

摘要

姜黄素是香料姜黄的活性成分,已被证明具有多种药理和治疗作用,包括抗氧化、抗菌、抗炎和抗癌特性。姜黄素的抗炎作用主要归因于其通过氧化还原调节抑制 NF-κB 活性。在这项研究中,我们表明姜黄素是一种免疫抑制植物化学物质,可通过阻断 T 细胞激活诱导的 Ca(2+)动员来发挥作用,IC(50)约为 12.5 μM,从而防止 NFAT 激活和 NFAT 调节的细胞因子表达。这一发现为姜黄素介导的抗炎和免疫抑制功能提供了新的机制。我们还表明,由于不同的抑制机制,姜黄素可以与 CsA 协同增强免疫抑制活性。此外,由于 Ca(2+)也是 TCR 诱导的 NF-κB 信号通路的关键第二信使,我们的发现还提供了姜黄素抑制 NF-κB 激活的另一种机制。

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