Suppr超能文献

对NLRP3炎性小体激活分子网络的最新见解。

Updated insights into the molecular networks for NLRP3 inflammasome activation.

作者信息

Paik Seungwha, Kim Jin Kyung, Shin Hyo Jung, Park Eun-Jin, Kim In Soo, Jo Eun-Kyeong

机构信息

Department of Microbiology, Chungnam National University College of Medicine, Daejeon, Republic of Korea.

Department of Medical Science, Chungnam National University College of Medicine, Daejeon, Republic of Korea.

出版信息

Cell Mol Immunol. 2025 Apr 30. doi: 10.1038/s41423-025-01284-9.

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.

摘要

在过去十年中,我们对含NACHT、富含亮氨酸重复序列和pyrin结构域的蛋白3(NLRP3)炎性小体的激活机制有了重大进展。这些发现为转录和翻译后调控过程、激活过程的结构-功能关系以及NLRP3激活的时空动态提供了详细的见解。值得注意的是,NLRP3炎性小体激活许可背后的多方面机制构成了深入研究的焦点。广泛的研究揭示了NLRP3及其炎性小体成分与伴侣分子在正负调控方面的相互作用。在本综述中,我们阐述了目前对在调节NLRP3炎性小体启动、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炎性小体激活及相关调控途径中涉及的复杂且相互关联的机制。此外,我们讨论了靶向NLRP3炎性小体的治疗策略开发的最新进展,以确定针对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新方法正在涌现。

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