一种天然代谢物和 NLRP3 炎症体抑制剂:4-羟基壬烯醛

Jinmin Zhang, Bradford C Berk, Chia George Hsu
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引用次数: 0

摘要

NOD-、LRR-和含吡咯啉结构域的蛋白 3(NLRP3)炎性组在先天性免疫反应中至关重要,它与多种人类疾病有关。然而,4-羟基壬烯醛(HNE)等内源性代谢物对 NLRP3 炎症小体活性的影响仍未得到充分探索。最近的研究强调了 HNE 在 NLRP3 炎症小体激活过程中的抑制作用,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 炎性体介导的脓毒症和 IL-1β 的分泌。此外,共价靶向是抑制 NLRP3 炎症小体组装的常见机制,为治疗干预提供了很好的途径。要了解内源性 HNE 对 NLRP3 炎症小体活化的影响,尤其是在产生 HNE 等脂质过氧化副产物的情况下,还需要进一步的研究。了解 HNE 与 NLRP3 炎症小体之间错综复杂的相互作用,对于揭示炎症性疾病的新型治疗策略具有重大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Natural Metabolite and Inhibitor of the NLRP3 Inflammasome: 4-hydroxynonenal.

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.

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