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本文引用的文献

1
NLRC5 senses NAD depletion, forming a PANoptosome and driving PANoptosis and inflammation.NLRC5 感知 NAD 耗竭,形成 PANoptosome,并驱动 PANoptosis 和炎症反应。
Cell. 2024 Jul 25;187(15):4061-4077.e17. doi: 10.1016/j.cell.2024.05.034. Epub 2024 Jun 14.
2
Genetic variations in NLRP3 and NLRP12 genes in adult-onset patients with autoinflammatory diseases: a comparative study.NLRP3 和 NLRP12 基因遗传变异与成人发病自身炎症性疾病的相关性:一项对比研究。
Front Immunol. 2024 Jan 26;14:1321370. doi: 10.3389/fimmu.2023.1321370. eCollection 2023.
3
The contributions of deleterious rare alleles in NLRP12 and inflammasome-related genes to polymyalgia rheumatica.NLRP12 和炎症小体相关基因中的有害稀有等位基因对多发性肌痛的贡献。
Sci Rep. 2024 Jan 4;14(1):490. doi: 10.1038/s41598-024-51320-3.
4
A guide to cell death pathways.细胞死亡途径指南。
Nat Rev Mol Cell Biol. 2024 May;25(5):379-395. doi: 10.1038/s41580-023-00689-6. Epub 2023 Dec 18.
5
Immune regulator IRF1 contributes to ZBP1-, AIM2-, RIPK1-, and NLRP12-PANoptosome activation and inflammatory cell death (PANoptosis).免疫调节因子 IRF1 有助于 ZBP1、AIM2、RIPK1 和 NLRP12 形成 PANoptosome 并激活炎症细胞死亡(PANoptosis)。
J Biol Chem. 2023 Sep;299(9):105141. doi: 10.1016/j.jbc.2023.105141. Epub 2023 Aug 7.
6
NLRP12-PANoptosome activates PANoptosis and pathology in response to heme and PAMPs.NLRP12-PANoptosome 响应血红素和 PAMPs 激活 PANoptosis 和病理学。
Cell. 2023 Jun 22;186(13):2783-2801.e20. doi: 10.1016/j.cell.2023.05.005. Epub 2023 Jun 1.
7
PANoptosome signaling and therapeutic implications in infection: central role for ZBP1 to activate the inflammasome and PANoptosis.PANoptosome 信号转导及其在感染中的治疗意义:ZBP1 激活炎症小体和 PANoptosis 的核心作用。
Curr Opin Immunol. 2023 Aug;83:102348. doi: 10.1016/j.coi.2023.102348. Epub 2023 May 31.
8
Innate immune inflammatory cell death: PANoptosis and PANoptosomes in host defense and disease.先天免疫炎症细胞死亡:宿主防御和疾病中的 PANoptosis 和 PANoptosomes。
Eur J Immunol. 2023 Nov;53(11):e2250235. doi: 10.1002/eji.202250235. Epub 2023 Mar 3.
9
Directionality of PYD filament growth determined by the transition of NLRP3 nucleation seeds to ASC elongation.由NLRP3成核种子向ASC延伸的转变所决定的PYD细丝生长的方向性。
Sci Adv. 2022 May 13;8(19):eabn7583. doi: 10.1126/sciadv.abn7583.
10
NLRP12-associated systemic autoinflammatory diseases in children.儿童 NLRP12 相关性系统性自身炎症性疾病。
Pediatr Rheumatol Online J. 2022 Feb 5;20(1):9. doi: 10.1186/s12969-022-00669-8.

炎性小体及其在 PANoptosomes 中的作用。

Inflammasomes and their role in PANoptosomes.

机构信息

Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

Department of Immunology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.

出版信息

Curr Opin Immunol. 2024 Dec;91:102489. doi: 10.1016/j.coi.2024.102489. Epub 2024 Sep 27.

DOI:10.1016/j.coi.2024.102489
PMID:39340880
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11609005/
Abstract

Inflammasomes are multiprotein signaling structures in the innate immune system that drive cell death and inflammatory responses. These protein complexes generally comprise an innate immune sensor, the adaptor protein ASC, and the inflammatory protease caspase-1. Inflammasomes are formed when a cytosolic sensor, also known as a pattern recognition receptor, senses its cognate ligand, which can include microbial components, endogenous damage/danger signals, or environmental stimuli. Inflammasome assembly leads to autoproteolytic cleavage and activation of caspase-1. This activation, in turn, induces proteolytic maturation and release of the proinflammatory cytokines interleukin (IL)-1β and IL-18, and the activation of the pore-forming molecule gasdermin D to induce cell death, known as pyroptosis. Recent studies have identified inflammasomes as integral components of larger cell death complexes, known as PANoptosomes. These PANoptosomes regulate PANoptosis, an innate immune cell death pathway initiated by innate immune sensors and driven by caspases and receptor-interacting serine/threonine protein kinases. PANoptosome assembly and activation leads to cell lysis, inflammation, and the release of proinflammatory cytokines, damage-associated molecular patterns, and alarmins. In this review, we discuss the current understanding of different inflammasomes and their role in PANoptosomes.

摘要

炎症小体是先天免疫系统中的多蛋白信号结构,可引发细胞死亡和炎症反应。这些蛋白复合物通常包括先天免疫传感器、衔接蛋白 ASC 和炎症蛋白酶 caspase-1。当胞质传感器(也称为模式识别受体)感应到其同源配体时,炎症小体就会形成,这些配体可以包括微生物成分、内源性损伤/危险信号或环境刺激物。炎症小体的组装导致 caspase-1 的自我蛋白水解切割和激活。这种激活反过来又诱导促炎细胞因子白细胞介素 (IL)-1β 和 IL-18 的蛋白水解成熟和释放,以及孔形成分子 gasdermin D 的激活,从而诱导细胞死亡,即细胞焦亡。最近的研究表明,炎症小体是更大的细胞死亡复合物(称为 PANoptosomes)的组成部分。这些 PANoptosomes 调节由先天免疫传感器启动并由半胱天冬酶和受体相互作用丝氨酸/苏氨酸蛋白激酶驱动的先天免疫细胞死亡途径 PANoptosis。PANoptosome 的组装和激活导致细胞裂解、炎症和促炎细胞因子、损伤相关分子模式和警报素的释放。在这篇综述中,我们讨论了不同炎症小体及其在 PANoptosomes 中的作用的最新理解。