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Toll 样受体和细胞内核酸传感器的微生物感应。

Microbial sensing by Toll-like receptors and intracellular nucleic acid sensors.

机构信息

Laboratory of Molecular Immunobiology, Graduate School of Biological Sciences, Nara Institute of Science and Technology (NAIST), Nara 630-0192, Japan Laboratory of Host Defense, WPI Immunology Frontier Research Center, Osaka University, Osaka 565-0871, Japan Department of Host Defense, Research Institute for Microbial Diseases, Osaka University, Osaka 565-0871, Japan.

Laboratory of Molecular Immunobiology, Graduate School of Biological Sciences, Nara Institute of Science and Technology (NAIST), Nara 630-0192, Japan Laboratory of Host Defense, WPI Immunology Frontier Research Center, Osaka University, Osaka 565-0871, Japan.

出版信息

Cold Spring Harb Perspect Biol. 2014 Oct 9;7(1):a016246. doi: 10.1101/cshperspect.a016246.


DOI:10.1101/cshperspect.a016246
PMID:25301932
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4292165/
Abstract

Recognition of an invading pathogen is critical to elicit protective responses. Certain microbial structures and molecules, which are crucial for their survival and virulence, are recognized by different families of evolutionarily conserved pattern recognition receptors (PRRs). This recognition initiates a signaling cascade that leads to the transcription of inflammatory cytokines and chemokines to eliminate pathogens and attract immune cells, thereby perpetuating further adaptive immune responses. Considerable research on the molecular mechanisms underlying host-pathogen interactions has resulted in the discovery of multifarious PRRs. In this review, we discuss the recent developments in microbial recognition by Toll-like receptors (TLRs) and intracellular nucleic acid sensors and the signaling pathways initiated by them.

摘要

识别入侵病原体对于引发保护反应至关重要。某些对微生物的生存和毒力至关重要的结构和分子,被不同家族的进化上保守的模式识别受体(PRR)识别。这种识别启动了一个信号级联反应,导致转录炎症细胞因子和趋化因子,以消除病原体并吸引免疫细胞,从而维持进一步的适应性免疫反应。对宿主-病原体相互作用的分子机制的大量研究导致了多种 PRR 的发现。在这篇综述中,我们讨论了 Toll 样受体(TLR)和细胞内核酸传感器对微生物的识别及其引发的信号通路的最新进展。

相似文献

[1]
Microbial sensing by Toll-like receptors and intracellular nucleic acid sensors.

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[2]
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[3]
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[4]
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[5]
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本文引用的文献

[1]
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Cell. 2014-2-13

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Nat Commun. 2013

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Mol Cell. 2013-6-6

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