Zhang Jinmin, Berk Bradford C, Hsu Chia George
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.
J Cell Immunol. 2024;6(2):76-81. doi: 10.33696/immunology.6.192.
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.
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。