Suppr超能文献

一种NLRP3炎性小体的天然代谢产物及抑制剂:4-羟基壬烯醛。

A Natural Metabolite and Inhibitor of the NLRP3 Inflammasome: 4-hydroxynonenal.

作者信息

Zhang Jinmin, Berk Bradford C, Hsu Chia George

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of North Texas Health Science Center, Fort Worth, TX, USA.

Department of Medicine, Aab Cardiovascular Research Institute, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.

出版信息

J Cell Immunol. 2024;6(2):76-81. doi: 10.33696/immunology.6.192.

Abstract

The NOD-, LRR-, and pyrin domain-containing protein 3 (NLRP3) inflammasome, crucial in the innate immune response, is linked to various human diseases. However, the effect of endogenous metabolites, like 4-hydroxynonenal (HNE), on NLRP3 inflammasome activity remains underexplored. Recent research highlights HNE's inhibitory role in NLRP3 inflammasome activation, shedding light on its potential as an endogenous regulator of inflammatory responses. Studies demonstrate that HNE blocks NLRP3 inflammasome-mediated pyroptosis and IL-1β secretion. Additionally, covalent targeting emerges as a common mechanism for inhibiting NLRP3 inflammasome assembly, offering promising avenues for therapeutic intervention. Further investigation is needed to understand the impact of endogenous HNE on NLRP3 inflammasome activation, especially in settings where lipid peroxidation byproducts like HNE are produced. Understanding the intricate interplay between HNE and the NLRP3 inflammasome holds significant potential for unraveling novel therapeutic strategies for inflammatory disorders.

摘要

含核苷酸结合寡聚化结构域样受体蛋白3(NLRP3)炎性小体在固有免疫反应中起关键作用,与多种人类疾病相关。然而,内源性代谢产物,如4-羟基壬烯醛(HNE)对NLRP3炎性小体活性的影响仍未得到充分研究。最近的研究突出了HNE在NLRP3炎性小体激活中的抑制作用,揭示了其作为炎症反应内源性调节剂的潜力。研究表明,HNE可阻断NLRP3炎性小体介导的细胞焦亡和白细胞介素-1β分泌。此外,共价靶向成为抑制NLRP3炎性小体组装的常见机制,为治疗干预提供了有前景的途径。需要进一步研究以了解内源性HNE对NLRP3炎性小体激活的影响,特别是在产生如HNE等脂质过氧化副产物的情况下。了解HNE与NLRP3炎性小体之间的复杂相互作用对于揭示炎症性疾病的新型治疗策略具有巨大潜力。

相似文献

1
A Natural Metabolite and Inhibitor of the NLRP3 Inflammasome: 4-hydroxynonenal.
J Cell Immunol. 2024;6(2):76-81. doi: 10.33696/immunology.6.192.
2
The lipid peroxidation product 4-hydroxynonenal inhibits NLRP3 inflammasome activation and macrophage pyroptosis.
Cell Death Differ. 2022 Sep;29(9):1790-1803. doi: 10.1038/s41418-022-00966-5. Epub 2022 Mar 9.
3
Activation of NLRP3 inflammasome contributes to the inflammatory response to allergic rhinitis via macrophage pyroptosis.
Int Immunopharmacol. 2022 Sep;110:109012. doi: 10.1016/j.intimp.2022.109012. Epub 2022 Jul 6.
4
5
The leucine-rich repeat (LRR) domain of NLRP3 is required for NLRP3 inflammasome activation in macrophages.
J Biol Chem. 2022 Dec;298(12):102717. doi: 10.1016/j.jbc.2022.102717. Epub 2022 Nov 17.
6
NOD-Like Receptor Protein 3 Inflammasome-Dependent IL-1β Accelerated ConA-Induced Hepatitis.
Front Immunol. 2018 Apr 10;9:758. doi: 10.3389/fimmu.2018.00758. eCollection 2018.
7
Inhibition of NLRP3 inflammasome-A potential mechanistic therapeutic for treatment of polycystic ovary syndrome?
J Biochem Mol Toxicol. 2024 Jan;38(1):e23592. doi: 10.1002/jbt.23592. Epub 2023 Dec 6.
8
The zebrafish NLRP3 inflammasome has functional roles in ASC-dependent interleukin-1β maturation and gasdermin E-mediated pyroptosis.
J Biol Chem. 2020 Jan 24;295(4):1120-1141. doi: 10.1074/jbc.RA119.011751. Epub 2019 Dec 18.
9
POP1 inhibits MSU-induced inflammasome activation and ameliorates gout.
Front Immunol. 2022 Sep 26;13:912069. doi: 10.3389/fimmu.2022.912069. eCollection 2022.
10
Hepatocyte pyroptosis and release of inflammasome particles induce stellate cell activation and liver fibrosis.
J Hepatol. 2021 Jan;74(1):156-167. doi: 10.1016/j.jhep.2020.07.041. Epub 2020 Aug 4.

引用本文的文献

2
Epidemiology, Symptoms and Pathophysiology of Long Covid Complications.
J Cell Immunol. 2024;6(5):219-230. doi: 10.33696/immunology.6.209.
3
Ozone therapy addresses neuropathic pain in ulcerous wounds.
Med Gas Res. 2025 Sep 1;15(3):448-449. doi: 10.4103/mgr.MEDGASRES-D-24-00145. Epub 2025 Apr 17.

本文引用的文献

1
A 360° view of the inflammasome: Mechanisms of activation, cell death, and diseases.
Cell. 2023 May 25;186(11):2288-2312. doi: 10.1016/j.cell.2023.04.025.
2
NLRP3 and pyroptosis blockers for treating inflammatory diseases.
Trends Pharmacol Sci. 2022 Aug;43(8):653-668. doi: 10.1016/j.tips.2022.04.003. Epub 2022 May 3.
3
The lipid peroxidation product 4-hydroxynonenal inhibits NLRP3 inflammasome activation and macrophage pyroptosis.
Cell Death Differ. 2022 Sep;29(9):1790-1803. doi: 10.1038/s41418-022-00966-5. Epub 2022 Mar 9.
4
Proteomic Analysis of Cardiac Adaptation to Exercise by High Resolution Mass Spectrometry.
Front Mol Biosci. 2021 Sep 1;8:723858. doi: 10.3389/fmolb.2021.723858. eCollection 2021.
5
Targeting prominin2 transcription to overcome ferroptosis resistance in cancer.
EMBO Mol Med. 2021 Aug 9;13(8):e13792. doi: 10.15252/emmm.202013792. Epub 2021 Jul 5.
6
Succination inactivates gasdermin D and blocks pyroptosis.
Science. 2020 Sep 25;369(6511):1633-1637. doi: 10.1126/science.abb9818. Epub 2020 Aug 20.
7
The Immunomodulatory Metabolite Itaconate Modifies NLRP3 and Inhibits Inflammasome Activation.
Cell Metab. 2020 Sep 1;32(3):468-478.e7. doi: 10.1016/j.cmet.2020.07.016. Epub 2020 Aug 12.
8
NLRP3 inflammasome priming: A riddle wrapped in a mystery inside an enigma.
J Leukoc Biol. 2020 Sep;108(3):937-952. doi: 10.1002/JLB.3MR0720-513R. Epub 2020 Aug 3.
9
Redox homeostasis maintained by GPX4 facilitates STING activation.
Nat Immunol. 2020 Jul;21(7):727-735. doi: 10.1038/s41590-020-0699-0. Epub 2020 Jun 15.
10
FDA-approved disulfiram inhibits pyroptosis by blocking gasdermin D pore formation.
Nat Immunol. 2020 Jul;21(7):736-745. doi: 10.1038/s41590-020-0669-6. Epub 2020 May 4.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验