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NLRP3 和 AIM2 炎性小体的结构、激活和调控。

Structure, Activation and Regulation of NLRP3 and AIM2 Inflammasomes.

机构信息

Department of Bioengineering, School of Engineering, University of California, Merced, 5200 North Lake Road, Merced, CA 95343, USA.

出版信息

Int J Mol Sci. 2021 Jan 16;22(2):872. doi: 10.3390/ijms22020872.

Abstract

The inflammasome is a three-component (sensor, adaptor, and effector) filamentous signaling platform that shields from multiple pathogenic infections by stimulating the proteolytical maturation of proinflammatory cytokines and pyroptotic cell death. The signaling process initiates with the detection of endogenous and/or external danger signals by specific sensors, followed by the nucleation and polymerization from sensor to downstream adaptor and then to the effector, caspase-1. Aberrant activation of inflammasomes promotes autoinflammatory diseases, cancer, neurodegeneration, and cardiometabolic disorders. Therefore, an equitable level of regulation is required to maintain the equilibrium between inflammasome activation and inhibition. Recent advancement in the structural and mechanistic understanding of inflammasome assembly potentiates the emergence of novel therapeutics against inflammasome-regulated diseases. In this review, we have comprehensively discussed the recent and updated insights into the structure of inflammasome components, their activation, interaction, mechanism of regulation, and finally, the formation of densely packed filamentous inflammasome complex that exists as micron-sized punctum in the cells and mediates the immune responses.

摘要

炎症小体是一种由三部分组成的(传感器、衔接蛋白和效应器)丝状信号平台,通过刺激前炎性细胞因子的蛋白水解成熟和细胞焦亡性细胞死亡,抵御多种致病感染。信号转导过程始于特定传感器对内源性和/或外源性危险信号的检测,随后从传感器到下游衔接蛋白再到效应器(半胱天冬酶-1)进行核形成和聚合。炎症小体的异常激活会促进自身炎症性疾病、癌症、神经退行性疾病和心血管代谢疾病的发生。因此,需要进行公平的调节,以维持炎症小体激活和抑制之间的平衡。炎症小体组装的结构和机制理解的最新进展促进了针对炎症小体调节疾病的新型治疗方法的出现。在这篇综述中,我们全面讨论了炎症小体组件的结构、激活、相互作用、调节机制以及最后存在于细胞中的微米大小的点状密集丝状炎症小体复合物的形成的最新和更新的见解,该复合物介导免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/43e5/7830601/fc20fe94e154/ijms-22-00872-g001.jpg

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