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A novel “complement–metabolism–inflammasome axis” as a key regulator of immune cell effector function

The inflammasomes are intracellular multiprotein complexes that induce and regulate the generation of the key pro‐inflammatory cytokines IL‐1β and IL‐18 in response to infectious microbes and cellular stress. The activation of inflammasomes involves several upstream signals including classic pattern...

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Detalles Bibliográficos
Autores principales: Arbore, Giuseppina, Kemper, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025719/
https://www.ncbi.nlm.nih.gov/pubmed/27184294
http://dx.doi.org/10.1002/eji.201546131
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author Arbore, Giuseppina
Kemper, Claudia
author_facet Arbore, Giuseppina
Kemper, Claudia
author_sort Arbore, Giuseppina
collection PubMed
description The inflammasomes are intracellular multiprotein complexes that induce and regulate the generation of the key pro‐inflammatory cytokines IL‐1β and IL‐18 in response to infectious microbes and cellular stress. The activation of inflammasomes involves several upstream signals including classic pattern or danger recognition systems such as the TLRs. Recently, however, the activation of complement receptors, such as the anaphylatoxin C3a and C5a receptors and the complement regulator CD46, in conjunction with the sensing of cell metabolic changes, for instance increased amino acid influx and glycolysis (via mTORC1), have emerged as additional critical activators of the inflammasome. This review summarizes recent advances in our knowledge about complement‐mediated inflammasome activation, with a specific focus on a novel “complement – metabolism – NLRP3 inflammasome axis.”
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spelling pubmed-50257192016-10-03 A novel “complement–metabolism–inflammasome axis” as a key regulator of immune cell effector function Arbore, Giuseppina Kemper, Claudia Eur J Immunol Highlights The inflammasomes are intracellular multiprotein complexes that induce and regulate the generation of the key pro‐inflammatory cytokines IL‐1β and IL‐18 in response to infectious microbes and cellular stress. The activation of inflammasomes involves several upstream signals including classic pattern or danger recognition systems such as the TLRs. Recently, however, the activation of complement receptors, such as the anaphylatoxin C3a and C5a receptors and the complement regulator CD46, in conjunction with the sensing of cell metabolic changes, for instance increased amino acid influx and glycolysis (via mTORC1), have emerged as additional critical activators of the inflammasome. This review summarizes recent advances in our knowledge about complement‐mediated inflammasome activation, with a specific focus on a novel “complement – metabolism – NLRP3 inflammasome axis.” John Wiley and Sons Inc. 2016-06-08 2016-07 /pmc/articles/PMC5025719/ /pubmed/27184294 http://dx.doi.org/10.1002/eji.201546131 Text en © 2016 The Authors. European Journal of Immunology published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Highlights
Arbore, Giuseppina
Kemper, Claudia
A novel “complement–metabolism–inflammasome axis” as a key regulator of immune cell effector function
title A novel “complement–metabolism–inflammasome axis” as a key regulator of immune cell effector function
title_full A novel “complement–metabolism–inflammasome axis” as a key regulator of immune cell effector function
title_fullStr A novel “complement–metabolism–inflammasome axis” as a key regulator of immune cell effector function
title_full_unstemmed A novel “complement–metabolism–inflammasome axis” as a key regulator of immune cell effector function
title_short A novel “complement–metabolism–inflammasome axis” as a key regulator of immune cell effector function
title_sort novel “complement–metabolism–inflammasome axis” as a key regulator of immune cell effector function
topic Highlights
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025719/
https://www.ncbi.nlm.nih.gov/pubmed/27184294
http://dx.doi.org/10.1002/eji.201546131
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