• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

含吡啉结构域的模式识别受体研究进展:从免疫到病理

An Update on PYRIN Domain-Containing Pattern Recognition Receptors: From Immunity to Pathology.

作者信息

Ratsimandresy Rojo A, Dorfleutner Andrea, Stehlik Christian

机构信息

Division of Rheumatology, Department of Medicine, Feinberg School of Medicine, Northwestern University , Chicago, IL , USA.

Division of Rheumatology, Department of Medicine, Feinberg School of Medicine, Northwestern University , Chicago, IL , USA ; Robert H. Lurie Comprehensive Cancer Center, Interdepartmental Immunobiology Center and Skin Disease Research Center, Feinberg School of Medicine, Northwestern University , Chicago, IL , USA.

出版信息

Front Immunol. 2013 Dec 9;4:440. doi: 10.3389/fimmu.2013.00440.

DOI:10.3389/fimmu.2013.00440
PMID:24367371
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3856626/
Abstract

Cytosolic pattern recognition receptors (PRRs) sense a wide range of endogenous danger-associated molecular patterns as well as exogenous pathogen-associated molecular patterns. In particular, Nod-like receptors containing a pyrin domain (PYD), called NLRPs, and AIM2-like receptors (ALRs) have been shown to play a critical role in host defense by facilitating clearance of pathogens and maintaining a healthy gut microflora. NLRPs and ALRs both encode a PYD, which is crucial for relaying signals that result in an efficient innate immune response through activation of several key innate immune signaling pathways. However, mutations in these PRRs have been linked to the development of auto-inflammatory and autoimmune diseases. In addition, they have been implicated in metabolic diseases. In this review, we summarize the function of PYD-containing NLRPs and ALRs and address their contribution to innate immunity, host defense, and immune-linked diseases.

摘要

胞质模式识别受体(PRR)可感知多种内源性危险相关分子模式以及外源性病原体相关分子模式。特别是,含有pyrin结构域(PYD)的Nod样受体(称为NLRP)和AIM2样受体(ALR)已被证明通过促进病原体清除和维持健康的肠道微生物群在宿主防御中发挥关键作用。NLRP和ALR都编码一个PYD,这对于通过激活几个关键的先天免疫信号通路来传递导致有效先天免疫反应的信号至关重要。然而,这些PRR中的突变与自身炎症性疾病和自身免疫性疾病的发生有关。此外,它们还与代谢性疾病有关。在本综述中,我们总结了含PYD的NLRP和ALR的功能,并阐述了它们对先天免疫、宿主防御和免疫相关疾病的贡献。

相似文献

1
An Update on PYRIN Domain-Containing Pattern Recognition Receptors: From Immunity to Pathology.含吡啉结构域的模式识别受体研究进展:从免疫到病理
Front Immunol. 2013 Dec 9;4:440. doi: 10.3389/fimmu.2013.00440.
2
Mechanisms and pathways of innate immune activation and regulation in health and cancer.健康与癌症中固有免疫激活和调节的机制与途径。
Hum Vaccin Immunother. 2014;10(11):3270-85. doi: 10.4161/21645515.2014.979640.
3
Inhibiting the inflammasome: one domain at a time.抑制炎性小体:一次一个结构域。
Immunol Rev. 2015 May;265(1):205-16. doi: 10.1111/imr.12290.
4
AIM2 Inflammasome's First Decade of Discovery: Focus on Oral Diseases.AIM2 炎性小体的发现十周年:聚焦口腔疾病。
Front Immunol. 2020 Aug 13;11:1487. doi: 10.3389/fimmu.2020.01487. eCollection 2020.
5
[Pattern recognition receptors].[模式识别受体]
Nihon Rinsho Meneki Gakkai Kaishi. 2011;34(5):329-45. doi: 10.2177/jsci.34.329.
6
Regulation of the NLRP3 Inflammasome by Post-Translational Modifications and Small Molecules.NLRP3 炎性小体的翻译后修饰和小分子调节。
Front Immunol. 2021 Feb 2;11:618231. doi: 10.3389/fimmu.2020.618231. eCollection 2020.
7
The Trinity of cGAS, TLR9, and ALRs Guardians of the Cellular Galaxy Against Host-Derived Self-DNA.cGAS、TLR9 和 ALRs 的三位一体:守护细胞星系对抗源自宿主的自身 DNA。
Front Immunol. 2021 Feb 11;11:624597. doi: 10.3389/fimmu.2020.624597. eCollection 2020.
8
Unraveling the NLRP family: Structure, function, activation, critical influence on tumor progression, and potential as targets for cancer therapy.解析 NLRP 家族:结构、功能、激活、对肿瘤进展的关键影响以及作为癌症治疗靶点的潜力。
Cancer Lett. 2024 Nov 28;605:217283. doi: 10.1016/j.canlet.2024.217283. Epub 2024 Oct 2.
9
complex formation of human PYRIN domain-only protein 3 prevented by self-oligomerization of ASC PYD domain.ASC PYD结构域的自寡聚化可阻止人仅含PYRIN结构域蛋白3的复合物形成。
Saudi J Biol Sci. 2021 Mar;28(3):1607-1614. doi: 10.1016/j.sjbs.2020.12.049. Epub 2021 Jan 5.
10
Structure of the absent in melanoma 2 (AIM2) pyrin domain provides insights into the mechanisms of AIM2 autoinhibition and inflammasome assembly.缺失黑色素瘤 2(AIM2)吡喃结构域的结构为 AIM2 自身抑制和炎性体组装机制提供了新的认识。
J Biol Chem. 2013 May 10;288(19):13225-35. doi: 10.1074/jbc.M113.468033. Epub 2013 Mar 25.

引用本文的文献

1
The potential immunomodulatory role of human milk oligosaccharides in prevention of viral infections and development of asthma in early life.人乳寡糖在预防病毒感染及早期生活中哮喘发展方面的潜在免疫调节作用。
Front Immunol. 2025 Jun 25;16:1572787. doi: 10.3389/fimmu.2025.1572787. eCollection 2025.
2
Inflammasome pathways in atopic dermatitis: insights into inflammatory mechanisms and therapeutic targets.特应性皮炎中的炎性小体通路:对炎症机制和治疗靶点的见解
An Bras Dermatol. 2025 Jun 23;100(4):501136. doi: 10.1016/j.abd.2025.501136.
3
Pyroptosis in Skeleton Diseases: A Potential Therapeutic Target Based on Inflammatory Cell Death.

本文引用的文献

1
Divergence of IL-1, IL-18, and cell death in NLRP3 inflammasomopathies.NLRP3 炎性体病中白细胞介素 1、白细胞介素 18 和细胞死亡的分歧。
J Clin Invest. 2013 Nov;123(11):4695-705. doi: 10.1172/JCI71543.
2
The mitochondrial antiviral protein MAVS associates with NLRP3 and regulates its inflammasome activity.线粒体抗病毒蛋白 MAVS 与 NLRP3 结合并调节其炎症小体活性。
J Immunol. 2013 Oct 15;191(8):4358-66. doi: 10.4049/jimmunol.1301170. Epub 2013 Sep 18.
3
Cytoplasmic LPS activates caspase-11: implications in TLR4-independent endotoxic shock.
骨病中的细胞焦亡:基于炎症细胞死亡的潜在治疗靶点。
Int J Mol Sci. 2024 Aug 21;25(16):9068. doi: 10.3390/ijms25169068.
4
cGAS-STING, inflammasomes and pyroptosis: an overview of crosstalk mechanism of activation and regulation.cGAS-STING、炎性体和细胞焦亡:激活和调控的串扰机制概述。
Cell Commun Signal. 2024 Jan 9;22(1):22. doi: 10.1186/s12964-023-01466-w.
5
Methods to Measure NLR Oligomerization I: Size Exclusion Chromatography, Co-immunoprecipitation, and Cross-Linking.方法测量 NLR 寡聚化 I:分子筛层析、共免疫沉淀和交联。
Methods Mol Biol. 2023;2696:55-71. doi: 10.1007/978-1-0716-3350-2_4.
6
MARCH5-dependent NLRP3 ubiquitination is required for mitochondrial NLRP3-NEK7 complex formation and NLRP3 inflammasome activation.MARCH5 依赖性 NLRP3 泛素化对于线粒体 NLRP3-NEK7 复合物的形成和 NLRP3 炎性小体的激活是必需的。
EMBO J. 2023 Oct 4;42(19):e113481. doi: 10.15252/embj.2023113481. Epub 2023 Aug 14.
7
Bibliometric evaluation of publications on inflammasomes in atherosclerosis from 2002 to 2022.2002年至2022年动脉粥样硬化中炎性小体相关出版物的文献计量学评价
Front Cardiovasc Med. 2023 Apr 12;10:1067226. doi: 10.3389/fcvm.2023.1067226. eCollection 2023.
8
Hepatic cecum: a key integrator of immunity in amphioxus.肝盲囊:文昌鱼免疫的关键整合器。
Mar Life Sci Technol. 2021 Jan 2;3(3):279-292. doi: 10.1007/s42995-020-00080-w. eCollection 2021 Aug.
9
The Role of NLRP3 Inflammasome Signaling on Arrhythmias in Diabetes.NLRP3炎性小体信号通路在糖尿病性心律失常中的作用
J Inflamm Res. 2022 Dec 29;15:6883-6889. doi: 10.2147/JIR.S390310. eCollection 2022.
10
Common NLRP3 inflammasome inhibitors and Covid-19: Divide and conquer.常见的NLRP3炎性小体抑制剂与新冠病毒病:各个击破。
Sci Afr. 2022 Nov;18:e01407. doi: 10.1016/j.sciaf.2022.e01407. Epub 2022 Oct 22.
细胞质脂多糖激活半胱天冬酶-11:在 TLR4 非依赖性内毒素性休克中的意义。
Science. 2013 Sep 13;341(6151):1250-3. doi: 10.1126/science.1240988.
4
LRRFIP2 negatively regulates NLRP3 inflammasome activation in macrophages by promoting Flightless-I-mediated caspase-1 inhibition.LRRFIP2 通过促进 Flightless-I 介导的 caspase-1 抑制来负调控巨噬细胞中的 NLRP3 炎性小体激活。
Nat Commun. 2013;4:2075. doi: 10.1038/ncomms3075.
5
Noncanonical inflammasome activation by intracellular LPS independent of TLR4.非经典炎性小体激活的细胞内 LPS 途径不依赖 TLR4。
Science. 2013 Sep 13;341(6151):1246-9. doi: 10.1126/science.1240248. Epub 2013 Jul 25.
6
Direct proteolytic cleavage of NLRP1B is necessary and sufficient for inflammasome activation by anthrax lethal factor.炭疽致死因子诱导 Nlrp1b 炎症小体激活需要并足以直接切割 Nlrp1b。
PLoS Pathog. 2013;9(6):e1003452. doi: 10.1371/journal.ppat.1003452. Epub 2013 Jun 20.
7
Omega-3 fatty acids prevent inflammation and metabolic disorder through inhibition of NLRP3 inflammasome activation.ω-3 脂肪酸通过抑制 NLRP3 炎性小体的激活来预防炎症和代谢紊乱。
Immunity. 2013 Jun 27;38(6):1154-63. doi: 10.1016/j.immuni.2013.05.015.
8
K⁺ efflux is the common trigger of NLRP3 inflammasome activation by bacterial toxins and particulate matter.K⁺ 外流是细菌毒素和颗粒物激活 NLRP3 炎性体的共同触发因素。
Immunity. 2013 Jun 27;38(6):1142-53. doi: 10.1016/j.immuni.2013.05.016.
9
Microbiota-induced activation of epithelial IL-6 signaling links inflammasome-driven inflammation with transmissible cancer.微生物群诱导的上皮细胞白细胞介素 6 信号激活将炎性体驱动的炎症与可传播的癌症联系起来。
Proc Natl Acad Sci U S A. 2013 Jun 11;110(24):9862-7. doi: 10.1073/pnas.1307575110. Epub 2013 May 21.
10
Human astrocytes express a novel NLRP2 inflammasome.人类星形胶质细胞表达一种新型 NLRP2 炎性小体。
Glia. 2013 Jul;61(7):1113-21. doi: 10.1002/glia.22499. Epub 2013 Apr 26.