Right place, right time: localisation and assembly of the NLRP3 inflammasome [version 1; peer review: 3 approved]

The NLRP3 inflammasome is a multimeric protein complex that cleaves caspase-1 and the pro-inflammatory cytokines interleukin 1 beta (IL-1β) and IL-18. Dysregulated NLRP3 inflammasome signalling is linked to several chronic inflammatory and autoimmune conditions; thus, understanding the activation me...

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Main Authors: Claire Hamilton, Paras K. Anand
Format: Article
Language:English
Published: F1000 Research Ltd 2019-05-01
Series:F1000Research
Online Access:https://f1000research.com/articles/8-676/v1
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spelling doaj-2e7d2cd1102d4e8d8a23d4e02815e6912020-11-25T01:19:33ZengF1000 Research LtdF1000Research2046-14022019-05-01810.12688/f1000research.18557.120314Right place, right time: localisation and assembly of the NLRP3 inflammasome [version 1; peer review: 3 approved]Claire Hamilton0Paras K. Anand1Infectious Diseases and Immunity, Department of Medicine, Imperial College London, The Commonwealth Building, Du Cane Road, London, W12 0NN, UKInfectious Diseases and Immunity, Department of Medicine, Imperial College London, The Commonwealth Building, Du Cane Road, London, W12 0NN, UKThe NLRP3 inflammasome is a multimeric protein complex that cleaves caspase-1 and the pro-inflammatory cytokines interleukin 1 beta (IL-1β) and IL-18. Dysregulated NLRP3 inflammasome signalling is linked to several chronic inflammatory and autoimmune conditions; thus, understanding the activation mechanisms of the NLRP3 inflammasome is essential. Studies over the past few years have implicated vital roles for distinct intracellular organelles in both the localisation and assembly of the NLRP3 inflammasome. However, conflicting reports exist. Prior to its activation, NLRP3 has been shown to be resident in the endoplasmic reticulum (ER) and cytosol, although, upon activation, the NLRP3 inflammasome has been shown to assemble in the cytosol, mitochondria, and mitochondria-associated ER membranes by different reports. Finally, very recent work has suggested that NLRP3 may be localised on or adjacent to the Golgi apparatus and that release of mediators from this organelle may contribute to inflammasome assembly. Therefore, NLRP3 may be strategically placed on or in close proximity to these subcellular compartments to both sense danger signals originating from these organelles and use the compartment as a scaffold to assemble the complex. Understanding where and when NLRP3 inflammasome assembly occurs may help identify potential targets for treatment of NLRP3-related disorders.https://f1000research.com/articles/8-676/v1
collection DOAJ
language English
format Article
sources DOAJ
author Claire Hamilton
Paras K. Anand
spellingShingle Claire Hamilton
Paras K. Anand
Right place, right time: localisation and assembly of the NLRP3 inflammasome [version 1; peer review: 3 approved]
F1000Research
author_facet Claire Hamilton
Paras K. Anand
author_sort Claire Hamilton
title Right place, right time: localisation and assembly of the NLRP3 inflammasome [version 1; peer review: 3 approved]
title_short Right place, right time: localisation and assembly of the NLRP3 inflammasome [version 1; peer review: 3 approved]
title_full Right place, right time: localisation and assembly of the NLRP3 inflammasome [version 1; peer review: 3 approved]
title_fullStr Right place, right time: localisation and assembly of the NLRP3 inflammasome [version 1; peer review: 3 approved]
title_full_unstemmed Right place, right time: localisation and assembly of the NLRP3 inflammasome [version 1; peer review: 3 approved]
title_sort right place, right time: localisation and assembly of the nlrp3 inflammasome [version 1; peer review: 3 approved]
publisher F1000 Research Ltd
series F1000Research
issn 2046-1402
publishDate 2019-05-01
description The NLRP3 inflammasome is a multimeric protein complex that cleaves caspase-1 and the pro-inflammatory cytokines interleukin 1 beta (IL-1β) and IL-18. Dysregulated NLRP3 inflammasome signalling is linked to several chronic inflammatory and autoimmune conditions; thus, understanding the activation mechanisms of the NLRP3 inflammasome is essential. Studies over the past few years have implicated vital roles for distinct intracellular organelles in both the localisation and assembly of the NLRP3 inflammasome. However, conflicting reports exist. Prior to its activation, NLRP3 has been shown to be resident in the endoplasmic reticulum (ER) and cytosol, although, upon activation, the NLRP3 inflammasome has been shown to assemble in the cytosol, mitochondria, and mitochondria-associated ER membranes by different reports. Finally, very recent work has suggested that NLRP3 may be localised on or adjacent to the Golgi apparatus and that release of mediators from this organelle may contribute to inflammasome assembly. Therefore, NLRP3 may be strategically placed on or in close proximity to these subcellular compartments to both sense danger signals originating from these organelles and use the compartment as a scaffold to assemble the complex. Understanding where and when NLRP3 inflammasome assembly occurs may help identify potential targets for treatment of NLRP3-related disorders.
url https://f1000research.com/articles/8-676/v1
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