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NLRP3炎性小体与细胞焦亡:在炎症和多系统疾病中的意义

NLRP3 inflammasome and pyroptosis: implications in inflammation and multisystem disorders.

作者信息

Li Xiaodi, Zhang Zhiyuan, Han Yang, Zhang Mianzhi

机构信息

Tianjin University of Traditional Chinese Medicine, Tianjin, China.

Tianjin Academy of Traditional Chinese Medicine Affiliated Hospital, Tianjin, China.

出版信息

PeerJ. 2025 Aug 15;13:e19887. doi: 10.7717/peerj.19887. eCollection 2025.


DOI:10.7717/peerj.19887
PMID:40832584
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12360325/
Abstract

The NLRP3 inflammasome is a multiprotein complex that senses diverse pathogen-associated molecular patterns (PAMPs) and danger-associated molecular patterns (DAMPs), activating the pyroptosis pathway. Pyroptosis is a form of programmed cell death that plays a crucial role in immune responses and inflammatory processes. The NLRP3 inflammasome-gasdermin D (GSDMD) axis has emerged as a critical therapeutic target in inflammatory diseases. Oligomerization of NLRP3 triggers caspase-1 activation, which subsequently induces GSDMD palmitoylation-an essential event that facilitates pyroptosis. Clinically, NLRP3 inhibitors, such as MCC950, demonstrate protective effects in NLRP3-mediated inflammatory diseases. GSDMD holds substantial potential as a diagnostic, monitoring, and therapeutic target across diverse diseases, underscoring its utility as a pan-biomarker. This review aims to synthesize current knowledge regarding the structure and function of the NLRP3 inflammasome and the regulatory mechanisms governing pyroptosis. Additionally, integrating findings from multiple physiological systems highlights the key roles of the NLRP3 inflammasome and pyroptosis in disease pathogenesis, offering novel perspectives for targeting inflammatory responses and associated disorders.

摘要

NLRP3炎性小体是一种多蛋白复合物,可感知多种病原体相关分子模式(PAMPs)和危险相关分子模式(DAMPs),从而激活细胞焦亡途径。细胞焦亡是一种程序性细胞死亡形式,在免疫反应和炎症过程中起关键作用。NLRP3炎性小体-gasdermin D(GSDMD)轴已成为炎症性疾病的关键治疗靶点。NLRP3的寡聚化触发半胱天冬酶-1激活,随后诱导GSDMD棕榈酰化,这是促进细胞焦亡的一个重要事件。临床上,NLRP3抑制剂,如MCC950,在NLRP3介导的炎症性疾病中显示出保护作用。GSDMD作为多种疾病的诊断、监测和治疗靶点具有巨大潜力,突显了其作为一种泛生物标志物的实用性。本综述旨在综合关于NLRP3炎性小体的结构和功能以及细胞焦亡调控机制的现有知识。此外,整合来自多个生理系统的研究结果突出了NLRP3炎性小体和细胞焦亡在疾病发病机制中的关键作用,为靶向炎症反应及相关疾病提供了新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d9e/12360325/4f8eb646fdef/peerj-13-19887-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d9e/12360325/a53b680b3f07/peerj-13-19887-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d9e/12360325/db0c4f5dce80/peerj-13-19887-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d9e/12360325/4f8eb646fdef/peerj-13-19887-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d9e/12360325/a53b680b3f07/peerj-13-19887-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d9e/12360325/db0c4f5dce80/peerj-13-19887-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d9e/12360325/4f8eb646fdef/peerj-13-19887-g003.jpg

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本文引用的文献

[1]
Exploring the therapeutic potential of NLRP3 inhibitors in Parkinson's Disease: a systematic review of in-vivo studies.

Inflammopharmacology. 2025-4-21

[2]
α -Lipoic acid alleviates Parkinson's disease by suppressing S100A9-mediated pyroptosis.

Int Immunopharmacol. 2025-5-16

[3]
New Insights on the Potential Role of Pyroptosis in Parkinson's Neuropathology and Therapeutic Targeting of NLRP3 Inflammasome with Recent Advances in Nanoparticle-Based miRNA Therapeutics.

Mol Neurobiol. 2025-3-18

[4]
The novel GSDMD inhibitor GI-Y2 exerts antipyroptotic effects to reduce atherosclerosis.

Clin Transl Med. 2025-3

[5]
Study on the effects of Mogroside V in inhibiting NLRP3-mediated granulosa cell pyroptosis and insulin resistance to improve PCOS.

J Ovarian Res. 2025-1-21

[6]
NEK7 phosphorylation amplifies NLRP3 inflammasome activation downstream of potassium efflux and gasdermin D.

Sci Immunol. 2025-1-3

[7]
Vitexin alleviates MNNG-induced chronic atrophic gastritis via inhibiting NLRP3 inflammasome.

J Ethnopharmacol. 2025-1-31

[8]
Brain Penetrant NLRP3 Inhibitors: The Discovery of a Panacea?

J Med Chem. 2024-12-12

[9]
Expression of NLRP3 in serum and induced sputum of children with asthma and their relationship with disease severity.

Eur J Med Res. 2024-11-1

[10]
PM Induces Pyroptosis via Activation of the ROS/NF-κB Signaling Pathway in Bronchial Epithelial Cells.

Medicina (Kaunas). 2024-9-2

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