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绿茶多酚表没食子儿茶素没食子酸酯通过抑制Elf-1表达上调Tollip表达。

Green Tea Polyphenol EGCG Upregulates Tollip Expression by Suppressing Elf-1 Expression.

作者信息

Kumazoe Motofumi, Yamashita Mai, Nakamura Yuki, Takamatsu Kanako, Bae Jaehoon, Yamashita Shuya, Yamada Shuhei, Onda Hiroaki, Nojiri Takashi, Kangawa Kenji, Tachibana Hirofumi

机构信息

Division of Applied Biological Chemistry, Department of Bioscience and Biotechnology, Faculty of Agriculture, Kyushu University, Fukuoka 812-8581, Japan; and.

Department of Biochemistry, National Cerebral and Cardiovascular Center Research Institute, Suita, 565-8565, Japan.

出版信息

J Immunol. 2017 Nov 1;199(9):3261-3269. doi: 10.4049/jimmunol.1601822. Epub 2017 Sep 27.

Abstract

TLR signaling is critical to innate immune system regulation; however, aberrant TLR signaling is involved in several diseases, including insulin resistance, Alzheimer's disease, and tumor metastasis. Moreover, a recent study found that TLR-4 signaling pathway inhibition might be a target for the suppression of chronic inflammatory disorders. In this article, we show that the green tea polyphenol epigallocatechin-3--gallate (EGCG) increases the expression of Toll interacting protein, a strong inhibitor of TLR4 signaling, by suppressing the expression of E74-like ETS transcription factor 1 (Elf-1). A mechanistic study revealed that EGCG suppressed Elf-1 expression via protein phosphatase 2A/cyclic GMP (cGMP)-dependent mechanisms. We also confirmed that orally administered EGCG and a cGMP inducer upregulated Toll interacting protein expression, increased intracellular levels of cGMP in macrophages, and suppressed Elf-1 expression. These data support EGCG and a cGMP inducer as potential candidate suppressors of TLR4 signaling.

摘要

Toll样受体(TLR)信号传导对于先天免疫系统的调节至关重要;然而,异常的TLR信号传导与多种疾病有关,包括胰岛素抵抗、阿尔茨海默病和肿瘤转移。此外,最近的一项研究发现,抑制TLR-4信号通路可能是抑制慢性炎症性疾病的一个靶点。在本文中,我们表明绿茶多酚表没食子儿茶素-3-没食子酸酯(EGCG)通过抑制E74样ETS转录因子1(Elf-1)的表达来增加Toll相互作用蛋白的表达,Toll相互作用蛋白是TLR4信号传导的强效抑制剂。一项机制研究表明,EGCG通过蛋白磷酸酶2A/环磷酸鸟苷(cGMP)依赖性机制抑制Elf-1的表达。我们还证实,口服EGCG和一种cGMP诱导剂可上调Toll相互作用蛋白的表达,增加巨噬细胞内cGMP水平,并抑制Elf-1的表达。这些数据支持EGCG和一种cGMP诱导剂作为TLR4信号传导的潜在候选抑制剂。

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