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1
Let's get this pyrin started!让我们开始这个(炎症)蛋白吧!
J Biol Chem. 2019 Mar 8;294(10):3367-3368. doi: 10.1074/jbc.H119.007830.
2
Bile acid analogues are activators of pyrin inflammasome.胆汁酸类似物是 pyrin 炎症小体的激活剂。
J Biol Chem. 2019 Mar 8;294(10):3359-3366. doi: 10.1074/jbc.RA118.005103. Epub 2019 Jan 15.
3
Connecting the immune system, systemic chronic inflammation and the gut microbiome: The role of sex.连接免疫系统、系统性慢性炎症和肠道微生物组:性别的作用。
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Inflammasomes and intestinal homeostasis: regulating and connecting infection, inflammation and the microbiota.炎性小体与肠道稳态:调节并连接感染、炎症与微生物群
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Cholera toxin B induces interleukin-1β production from resident peritoneal macrophages through the pyrin inflammasome as well as the NLRP3 inflammasome.霍乱毒素 B 通过 pyrin 炎性小体和 NLRP3 炎性小体诱导驻留腹腔巨噬细胞产生白细胞介素-1β。
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引用本文的文献

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The PYRIN domain is required for TLR4-mediated inflammation by PYHIN family members.PYHIN家族成员介导的TLR4炎症反应需要PYRIN结构域。
iScience. 2025 Apr 11;28(5):112413. doi: 10.1016/j.isci.2025.112413. eCollection 2025 May 16.

本文引用的文献

1
Bile acid analogues are activators of pyrin inflammasome.胆汁酸类似物是 pyrin 炎症小体的激活剂。
J Biol Chem. 2019 Mar 8;294(10):3359-3366. doi: 10.1074/jbc.RA118.005103. Epub 2019 Jan 15.
2
Pyrin Inflammasome Regulates Tight Junction Integrity to Restrict Colitis and Tumorigenesis.吡啉炎性小体调节紧密连接完整性以限制结肠炎和肿瘤发生。
Gastroenterology. 2018 Mar;154(4):948-964.e8. doi: 10.1053/j.gastro.2017.11.276. Epub 2017 Dec 2.
3
Inflammasomes on the Crossroads of Innate Immune Recognition and Metabolic Control.炎症小体在先天免疫识别和代谢控制的十字路口。
Cell Metab. 2017 Jul 5;26(1):71-93. doi: 10.1016/j.cmet.2017.06.018.
4
Familial Mediterranean fever mutations lift the obligatory requirement for microtubules in Pyrin inflammasome activation.家族性地中海热突变解除了微管蛋白在吡啉炎性小体激活中的必要需求。
Proc Natl Acad Sci U S A. 2016 Dec 13;113(50):14384-14389. doi: 10.1073/pnas.1613156113. Epub 2016 Nov 22.
5
Inflammasomes: mechanism of assembly, regulation and signalling.炎症小体:组装、调控和信号转导机制。
Nat Rev Immunol. 2016 Jul;16(7):407-20. doi: 10.1038/nri.2016.58. Epub 2016 Jun 13.
6
Microbiota-Modulated Metabolites Shape the Intestinal Microenvironment by Regulating NLRP6 Inflammasome Signaling.微生物群调节的代谢产物通过调节NLRP6炎性小体信号塑造肠道微环境。
Cell. 2015 Dec 3;163(6):1428-43. doi: 10.1016/j.cell.2015.10.048.
7
Metabolite-sensing receptors GPR43 and GPR109A facilitate dietary fibre-induced gut homeostasis through regulation of the inflammasome.代谢物感应受体 GPR43 和 GPR109A 通过调节炎症小体促进膳食纤维诱导的肠道稳态。
Nat Commun. 2015 Apr 1;6:6734. doi: 10.1038/ncomms7734.
8
Lactate reduces liver and pancreatic injury in Toll-like receptor- and inflammasome-mediated inflammation via GPR81-mediated suppression of innate immunity.乳酸通过 GPR81 介导的先天免疫抑制减轻 Toll 样受体和炎症小体介导的炎症中的肝和胰腺损伤。
Gastroenterology. 2014 Jun;146(7):1763-74. doi: 10.1053/j.gastro.2014.03.014. Epub 2014 Mar 20.

让我们开始这个(炎症)蛋白吧!

Let's get this pyrin started!

机构信息

From the Microbiome and Mucosal Defense Research Unit, Montreal Clinical Research Institute (IRCM), Montréal, Quebec H2W 1R7, Canada,

Department of Medicine, Université de Montréal, Montréal, Quebec H3C 3J7, Canada, and.

出版信息

J Biol Chem. 2019 Mar 8;294(10):3367-3368. doi: 10.1074/jbc.H119.007830.

DOI:10.1074/jbc.H119.007830
PMID:30850508
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6416431/
Abstract

Inflammasomes enable cells to respond to pathogens or biological damage, but the specific signals being used to convey these messages are not always clear. A new paper identifies two potential microbiota-derived metabolites, the bile acid analogues BAA485 and BAA473, as the first small molecules to activate the pyrin inflammasome. These results suggest that microbiota may be able to modulate this inflammatory process which, in turn, may contribute to the maintenance of intestinal homeostasis.

摘要

炎症小体使细胞能够对病原体或生物损伤做出反应,但用于传递这些信息的特定信号并不总是清楚的。一篇新论文确定了两种潜在的微生物衍生代谢物,胆汁酸类似物 BAA485 和 BAA473,作为第一个激活吡喃炎症小体的小分子。这些结果表明,微生物群可能能够调节这种炎症过程,反过来,这可能有助于维持肠道内稳态。