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How Factors Involved in the Resolution of Crystal-Induced Inflammation Target IL-1β

One of the main clinical features characterizing crystal-induced inflammation is its spontaneous resolution. The aim of this review is to outline the various factors involved in the self-limiting course of crystal-induced inflammation focusing on their effect on IL-1β production. Endogenous molecule...

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Detalles Bibliográficos
Autores principales: Oliviero, Francesca, Scanu, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368178/
https://www.ncbi.nlm.nih.gov/pubmed/28400732
http://dx.doi.org/10.3389/fphar.2017.00164
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author Oliviero, Francesca
Scanu, Anna
author_facet Oliviero, Francesca
Scanu, Anna
author_sort Oliviero, Francesca
collection PubMed
description One of the main clinical features characterizing crystal-induced inflammation is its spontaneous resolution. The aim of this review is to outline the various factors involved in the self-limiting course of crystal-induced inflammation focusing on their effect on IL-1β production. Endogenous molecules that are induced or locally recruited by the process itself, inhibitory proteins naturally present in the joint and exogenous dietary factors are discussed. Aside from the classical well-known molecules involved in the resolution of crystal-induced acute attack such as TGFβ, IL-10, IL-1Ra, and lipoproteins, particular attention is paid to recently uncovered mechanisms such as the aggregation of neutrophil extracellular traps, the release of ectosomes from neutrophil surface, and alpha-1-anti-trypsin-mediated IL-1 inhibition.
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spelling pubmed-53681782017-04-11 How Factors Involved in the Resolution of Crystal-Induced Inflammation Target IL-1β Oliviero, Francesca Scanu, Anna Front Pharmacol Pharmacology One of the main clinical features characterizing crystal-induced inflammation is its spontaneous resolution. The aim of this review is to outline the various factors involved in the self-limiting course of crystal-induced inflammation focusing on their effect on IL-1β production. Endogenous molecules that are induced or locally recruited by the process itself, inhibitory proteins naturally present in the joint and exogenous dietary factors are discussed. Aside from the classical well-known molecules involved in the resolution of crystal-induced acute attack such as TGFβ, IL-10, IL-1Ra, and lipoproteins, particular attention is paid to recently uncovered mechanisms such as the aggregation of neutrophil extracellular traps, the release of ectosomes from neutrophil surface, and alpha-1-anti-trypsin-mediated IL-1 inhibition. Frontiers Media S.A. 2017-03-28 /pmc/articles/PMC5368178/ /pubmed/28400732 http://dx.doi.org/10.3389/fphar.2017.00164 Text en Copyright © 2017 Oliviero and Scanu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Oliviero, Francesca
Scanu, Anna
How Factors Involved in the Resolution of Crystal-Induced Inflammation Target IL-1β
title How Factors Involved in the Resolution of Crystal-Induced Inflammation Target IL-1β
title_full How Factors Involved in the Resolution of Crystal-Induced Inflammation Target IL-1β
title_fullStr How Factors Involved in the Resolution of Crystal-Induced Inflammation Target IL-1β
title_full_unstemmed How Factors Involved in the Resolution of Crystal-Induced Inflammation Target IL-1β
title_short How Factors Involved in the Resolution of Crystal-Induced Inflammation Target IL-1β
title_sort how factors involved in the resolution of crystal-induced inflammation target il-1β
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5368178/
https://www.ncbi.nlm.nih.gov/pubmed/28400732
http://dx.doi.org/10.3389/fphar.2017.00164
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