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NOD 样受体:感染期间细胞内稳态紊乱的守护者。

NOD-Like Receptors: Guards of Cellular Homeostasis Perturbation during Infection.

机构信息

Institute of Immunology, Friedrich-Loeffler-Institut, 17493 Greifswald, Germany.

Faculty of Mathematics and Natural Sciences, University of Greifswald, 17489 Greifswald, Germany.

出版信息

Int J Mol Sci. 2021 Jun 23;22(13):6714. doi: 10.3390/ijms22136714.

Abstract

The innate immune system relies on families of pattern recognition receptors (PRRs) that detect distinct conserved molecular motifs from microbes to initiate antimicrobial responses. Activation of PRRs triggers a series of signaling cascades, leading to the release of pro-inflammatory cytokines, chemokines and antimicrobials, thereby contributing to the early host defense against microbes and regulating adaptive immunity. Additionally, PRRs can detect perturbation of cellular homeostasis caused by pathogens and fine-tune the immune responses. Among PRRs, nucleotide binding oligomerization domain (NOD)-like receptors (NLRs) have attracted particular interest in the context of cellular stress-induced inflammation during infection. Recently, mechanistic insights into the monitoring of cellular homeostasis perturbation by NLRs have been provided. We summarize the current knowledge about the disruption of cellular homeostasis by pathogens and focus on NLRs as innate immune sensors for its detection. We highlight the mechanisms employed by various pathogens to elicit cytoskeleton disruption, organelle stress as well as protein translation block, point out exemplary NLRs that guard cellular homeostasis during infection and introduce the concept of stress-associated molecular patterns (SAMPs). We postulate that integration of information about microbial patterns, danger signals, and SAMPs enables the innate immune system with adequate plasticity and precision in elaborating responses to microbes of variable virulence.

摘要

天然免疫系统依赖于一系列模式识别受体 (PRR),这些受体能够识别微生物中独特的保守分子模式,从而引发抗微生物反应。PRR 的激活触发了一系列信号级联反应,导致促炎细胞因子、趋化因子和抗微生物物质的释放,从而有助于宿主对微生物的早期防御和调节适应性免疫。此外,PRR 还可以检测病原体引起的细胞内稳态的改变,并对免疫反应进行微调。在 PRR 中,核苷酸结合寡聚化结构域 (NOD)-样受体 (NLR) 在感染过程中细胞应激诱导的炎症方面引起了特别的关注。最近,人们对 NLR 监测细胞内稳态改变的机制有了更深入的了解。我们总结了病原体对内稳态破坏的最新认识,并重点介绍了 NLR 作为先天免疫传感器来检测内稳态改变的机制。我们强调了各种病原体用来引发细胞骨架破坏、细胞器应激和蛋白质翻译阻断的机制,指出了在感染过程中保护细胞内稳态的典型 NLR,并介绍了应激相关分子模式 (SAMPs) 的概念。我们假设,微生物模式、危险信号和 SAMPs 的信息整合使先天免疫系统在对不同毒力的微生物产生反应时具有足够的灵活性和精确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62e7/8268748/ab72594ad8c0/ijms-22-06714-g001.jpg

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