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Toll 样受体 10 识别双链 RNA 及调控干扰素通路。

Recognition of Double-Stranded RNA and Regulation of Interferon Pathway by Toll-Like Receptor 10.

机构信息

HKU-Pasteur Research Pole and Center of Influenza Research, Li Ka Shing Faculty of Medicine, School of Public Health, The University of Hong Kong, Pokfulam, Hong Kong.

Li Ka Shing Faculty of Medicine, School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong.

出版信息

Front Immunol. 2018 Mar 16;9:516. doi: 10.3389/fimmu.2018.00516. eCollection 2018.

Abstract

Toll-like receptor (TLR)-10 remains an orphan receptor without well-characterized ligands or functions. Here, we reveal that TLR10 is predominantly localized to endosomes and binds dsRNA at endosomal pH, suggesting that dsRNA is a ligand of TLR10. Recognition of dsRNA by TLR10 activates recruitment of myeloid differentiation primary response gene 88 for signal transduction and suppression of interferon regulatory factor-7 dependent type I IFN production. We also demonstrate crosstalk between TLR10 and TLR3, as they compete with each other for dsRNA binding. Our results suggest for the first time that dsRNA is a ligand for TLR10 and propose novel dual functions of TLR10 in regulating IFN signaling: first, recognition of dsRNA as a nucleotide-sensing receptor and second, sequestration of dsRNA from TLR3 to inhibit TLR3 signaling in response to dsRNA stimulation.

摘要

Toll 样受体(TLR)-10 仍然是一种孤儿受体,没有特征明确的配体或功能。在这里,我们揭示 TLR10 主要定位于内体,并在内体 pH 下结合 dsRNA,这表明 dsRNA 是 TLR10 的配体。TLR10 对 dsRNA 的识别激活了髓样分化初级反应基因 88 的募集,用于信号转导,并抑制干扰素调节因子-7 依赖性 I 型 IFN 的产生。我们还证明了 TLR10 和 TLR3 之间的串扰,因为它们相互竞争 dsRNA 的结合。我们的研究结果首次表明 dsRNA 是 TLR10 的配体,并提出了 TLR10 在调节 IFN 信号中的新的双重功能:首先,作为核苷酸感应受体识别 dsRNA,其次,将 dsRNA 从 TLR3 中隔离出来,以抑制 TLR3 信号对 dsRNA 刺激的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c953/5865411/3b9f9b8f3617/fimmu-09-00516-g001.jpg

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