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炎症的氧化应激之星:炎性小体与线粒体崩溃之间的联系。

The rOX-stars of inflammation: links between the inflammasome and mitochondrial meltdown.

作者信息

Holley Caroline L, Schroder Kate

机构信息

Institute for Molecular Bioscience IMB Centre for Inflammation and Disease Research The University of Queensland St. Lucia QLD Australia.

出版信息

Clin Transl Immunology. 2020 Feb 10;9(2):e01109. doi: 10.1002/cti2.1109. eCollection 2020.

Abstract

The nod-like receptor protein 3 (NLRP3) inflammasome drives inflammation in response to mitochondrial dysfunction. As metabolic powerhouses with prokaryotic ancestry, mitochondria are a cache for danger-associated molecular patterns and pathogen-associated molecular pattern-like molecules that elicit potent innate immune responses. Persistent mitochondrial damage caused by infection, or genetic or environmental factors, can lead to inappropriate or sustained inflammasome signalling. Here, we review the features of mitochondria that drive inflammatory signalling, with a particular focus on mitochondrial activation of the NLRP3 inflammasome. Given that mitochondrial network dynamics, metabolic activity and redox state are all intricately linked to each other and to NLRP3 inflammasome activity, we highlight the importance of a holistic approach to investigations of NLRP3 activation by dysfunctional mitochondria.

摘要

NOD样受体蛋白3(NLRP3)炎性小体在响应线粒体功能障碍时会引发炎症。线粒体作为具有原核生物起源的代谢动力源,是危险相关分子模式和病原体相关分子模式样分子的储存库,这些分子会引发强烈的先天性免疫反应。由感染、遗传或环境因素导致的持续性线粒体损伤可导致不适当或持续的炎性小体信号传导。在此,我们综述了驱动炎症信号传导的线粒体特征,尤其关注NLRP3炎性小体的线粒体激活。鉴于线粒体网络动态、代谢活性和氧化还原状态彼此之间以及与NLRP3炎性小体活性都有着复杂的联系,我们强调了采用整体方法研究功能失调的线粒体激活NLRP3的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8798/7008497/8980400b80a2/CTI2-9-e01109-g001.jpg

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