Updated insights into the molecular networks for NLRP3 inflammasome activation.

IF 21.8 1区 医学 Q1 IMMUNOLOGY
Cellular &Molecular Immunology Pub Date : 2025-06-01 Epub Date: 2025-04-30 DOI:10.1038/s41423-025-01284-9
Seungwha Paik, Jin Kyung Kim, Hyo Jung Shin, Eun-Jin Park, In Soo Kim, Eun-Kyeong Jo
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引用次数: 0

Abstract

Over the past decade, significant advances have been made in our understanding of how NACHT-, leucine-rich-repeat-, and pyrin domain-containing protein 3 (NLRP3) inflammasomes are activated. These findings provide detailed insights into the transcriptional and posttranslational regulatory processes, the structural-functional relationship of the activation processes, and the spatiotemporal dynamics of NLRP3 activation. Notably, the multifaceted mechanisms underlying the licensing of NLRP3 inflammasome activation constitute a focal point of intense research. Extensive research has revealed the interactions of NLRP3 and its inflammasome components with partner molecules in terms of positive and negative regulation. In this Review, we provide the current understanding of the complex molecular networks that play pivotal roles in regulating NLRP3 inflammasome priming, licensing and assembly. In addition, we highlight the intricate and interconnected mechanisms involved in the activation of the NLRP3 inflammasome and the associated regulatory pathways. Furthermore, we discuss recent advances in the development of therapeutic strategies targeting the NLRP3 inflammasome to identify potential therapeutics for NLRP3-associated inflammatory diseases. As research continues to uncover the intricacies of the molecular networks governing NLRP3 activation, novel approaches for therapeutic interventions against NLRP3-related pathologies are emerging.

NLRP3炎性小体激活分子网络的最新见解。
在过去的十年中,我们对NACHT-、富含亮氨酸的重复序列-和含pyrin结构域蛋白3 (NLRP3)炎症小体如何被激活的理解取得了重大进展。这些发现为NLRP3的转录和翻译后调控过程、激活过程的结构-功能关系以及激活的时空动态提供了详细的见解。值得注意的是,NLRP3炎性小体激活背后的多方面机制构成了激烈研究的焦点。广泛的研究揭示了NLRP3及其炎性小体组分与伴侣分子在正调控和负调控方面的相互作用。在这篇综述中,我们提供了目前对在调节NLRP3炎症小体启动、许可和组装中起关键作用的复杂分子网络的理解。此外,我们强调了NLRP3炎性小体激活和相关调控途径中涉及的复杂和相互关联的机制。此外,我们讨论了针对NLRP3炎症小体的治疗策略的最新进展,以确定NLRP3相关炎症性疾病的潜在治疗方法。随着研究不断揭示控制NLRP3激活的分子网络的复杂性,针对NLRP3相关病理的治疗干预的新方法正在出现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
31.20
自引率
1.20%
发文量
903
审稿时长
1 months
期刊介绍: Cellular & Molecular Immunology, a monthly journal from the Chinese Society of Immunology and the University of Science and Technology of China, serves as a comprehensive platform covering both basic immunology research and clinical applications. The journal publishes a variety of article types, including Articles, Review Articles, Mini Reviews, and Short Communications, focusing on diverse aspects of cellular and molecular immunology.
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