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NLRP3炎性小体:在疼痛治疗中的作用及治疗潜力

The NLRP3 Inflammasome: Role and Therapeutic Potential in Pain Treatment.

作者信息

Starobova Hana, Nadar Evelyn Israel, Vetter Irina

机构信息

Centre for Pain Research, Institute for Molecular Bioscience, University of Queensland, St Lucia, QLD, Australia.

School of Pharmacy, The University of Queensland, St Lucia, QLD, Australia.

出版信息

Front Physiol. 2020 Aug 19;11:1016. doi: 10.3389/fphys.2020.01016. eCollection 2020.

Abstract

Pain is a fundamental feature of inflammation. The immune system plays a critical role in the activation of sensory neurons and there is increasing evidence of neuro-inflammatory mechanisms contributing to painful pathologies. The inflammasomes are signaling multiprotein complexes that are key components of the innate immune system. They are intimately involved in inflammatory responses and their activation leads to production of inflammatory cytokines that in turn can affect sensory neuron function. Accordingly, the contribution of inflammasome activation to pain signaling has attracted considerable attention in recent years. NLRP3 is the best characterized inflammasome and there is emerging evidence of its role in a variety of inflammatory pain conditions. In vitro and in vivo studies have reported the activation and upregulation of NLRP3 in painful conditions including gout and rheumatoid arthritis, while inhibition of NLRP3 function or expression can mediate analgesia. In this review, we discuss painful conditions in which NLRP3 inflammasome signaling has been pathophysiologically implicated, as well as NLRP3 inflammasome-mediated mechanisms and signaling pathways that may lead to the activation of sensory neurons.

摘要

疼痛是炎症的一个基本特征。免疫系统在感觉神经元的激活中起关键作用,并且越来越多的证据表明神经炎症机制与疼痛性疾病有关。炎性小体是信号传导多蛋白复合物,是先天免疫系统的关键组成部分。它们密切参与炎症反应,其激活导致炎性细胞因子的产生,进而可影响感觉神经元功能。因此,近年来炎性小体激活对疼痛信号传导的作用引起了相当大的关注。NLRP3是特征最明确的炎性小体,并且有新证据表明其在多种炎性疼痛病症中的作用。体外和体内研究报告了在痛风和类风湿性关节炎等疼痛病症中NLRP3的激活和上调,而抑制NLRP3功能或表达可介导镇痛作用。在本综述中,我们讨论了NLRP3炎性小体信号传导在病理生理上与之相关的疼痛病症,以及可能导致感觉神经元激活的NLRP3炎性小体介导的机制和信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/772d/7468416/ab133fa84d77/fphys-11-01016-g001.jpg

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