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盘基网柄菌衍生因子对Jurkat细胞中白细胞介素-2产生的调控。

Regulation of IL-2 production in Jurkat cells by Dictyostelium-derived factors.

作者信息

Takahashi Katsunori, Murakami Masami, Hosaka Kohei, Kikuchi Haruhisa, Oshima Yoshiteru, Kubohara Yuzuru

机构信息

Department of Clinical Laboratory, Gunma University School of Medicine, Maebashi 371-8511, Japan.

出版信息

Life Sci. 2009 Sep 9;85(11-12):438-43. doi: 10.1016/j.lfs.2009.07.008. Epub 2009 Jul 24.

Abstract

AIMS

Differentiation-inducing factors (DIFs) are chlorinated alkylphenones found in the cellular slime mold Dictyostelium discoideum. DIF derivatives exhibit antiproliferative activities and promote glucose consumption in mammalian cells in vitro. In this study, we assessed the ability of DIFs to regulate the immune system and investigated their mechanisms of action.

MAIN METHODS

We examined the effects of 30 DIF derivatives on concanavalin A-induced IL-2 production (CIIP) in Jurkat T-cells. We also examined the effects of some DIF derivatives on the activity of AP-1 (activator protein-1), NFAT (nuclear factor of activated T-cells), and NFkappaB (nuclear factor kappa B), which are transcription factors required for CIIP.

KEY FINDINGS

Of the derivatives tested, some compounds suppressed CIIP as well as the known immunosuppressants cyclosporine A and FK506. A reporter gene assay revealed that 4 DIF derivatives tested suppressed CIIP, at least in part, by inhibiting the activity of AP-1, NFAT, and/or NFkappaB. Unlike cyclosporine A and FK506, the DIF derivatives had little effect on concanavalin A-induced interferon-gamma production in Jurkat cells.

SIGNIFICANCE

The present results suggest that DIF derivatives could be developed as novel immunosuppressive drugs.

摘要

目的

分化诱导因子(DIFs)是在细胞黏菌盘基网柄菌中发现的氯化烷基酚。DIF衍生物在体外对哺乳动物细胞具有抗增殖活性并促进葡萄糖消耗。在本研究中,我们评估了DIFs调节免疫系统的能力并研究了它们的作用机制。

主要方法

我们检测了30种DIF衍生物对Jurkat T细胞中伴刀豆球蛋白A诱导的IL-2产生(CIIP)的影响。我们还检测了一些DIF衍生物对AP-1(激活蛋白-1)、NFAT(活化T细胞的核因子)和NFκB(核因子κB)活性的影响,这些是CIIP所需的转录因子。

主要发现

在所测试的衍生物中,一些化合物抑制CIIP的效果与已知的免疫抑制剂环孢素A和FK506相当。报告基因检测显示,所测试的4种DIF衍生物至少部分通过抑制AP-1、NFAT和/或NFκB的活性来抑制CIIP。与环孢素A和FK506不同,DIF衍生物对Jurkat细胞中伴刀豆球蛋白A诱导的干扰素-γ产生几乎没有影响。

意义

目前的结果表明,DIF衍生物可被开发为新型免疫抑制药物。

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