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Toll样受体、STING、MAVS、炎性小体和干扰素通路的分子机制

Molecular Mechanisms of the Toll-Like Receptor, STING, MAVS, Inflammasome, and Interferon Pathways.

作者信息

Manes Nathan P, Nita-Lazar Aleksandra

机构信息

Functional Cellular Networks Section, Laboratory of Immune System Biology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland, USA.

出版信息

mSystems. 2021 Jun 29;6(3):e0033621. doi: 10.1128/mSystems.00336-21.

Abstract

Pattern recognition receptors (PRRs) form the front line of defense against pathogens. Many of the molecular mechanisms that facilitate PRR signaling have been characterized in detail, which is critical for the development of accurate PRR pathway models at the molecular interaction level. These models could support the development of therapeutics for numerous diseases, including sepsis and COVID-19. This review describes the molecular mechanisms of the principal signaling interactions of the Toll-like receptor, STING, MAVS, and inflammasome pathways. A detailed molecular mechanism network is included as Data Set S1 in the supplemental material.

摘要

模式识别受体(PRRs)构成了抵御病原体的第一道防线。许多促进PRR信号传导的分子机制已得到详细表征,这对于在分子相互作用水平上建立准确的PRR通路模型至关重要。这些模型可为包括败血症和新冠肺炎在内的多种疾病的治疗方法开发提供支持。本综述描述了Toll样受体、STING、MAVS和炎性小体通路主要信号相互作用的分子机制。补充材料中的数据集S1包含了详细的分子机制网络。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8c7a/8269223/abe7a486c371/msystems.00336-21-f001.jpg

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