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Titanium ions form particles that activate and execute interleukin‐1β release from lipopolysaccharide‐primed macrophages

BACKGROUND AND OBJECTIVE: Peri‐implantitis is a destructive inflammatory process characterized by destruction of the implant‐supporting bone. Inflammasomes are large intracellular multiprotein complexes that play a central role in innate immunity by activating the release of proinflammatory cytokine...

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Autores principales: Pettersson, M., Kelk, P., Belibasakis, G. N., Bylund, D., Molin Thorén, M., Johansson, A.
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/PMC5297875/
https://www.ncbi.nlm.nih.gov/pubmed/26987886
http://dx.doi.org/10.1111/jre.12364
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author Pettersson, M.
Kelk, P.
Belibasakis, G. N.
Bylund, D.
Molin Thorén, M.
Johansson, A.
author_facet Pettersson, M.
Kelk, P.
Belibasakis, G. N.
Bylund, D.
Molin Thorén, M.
Johansson, A.
author_sort Pettersson, M.
collection PubMed
description BACKGROUND AND OBJECTIVE: Peri‐implantitis is a destructive inflammatory process characterized by destruction of the implant‐supporting bone. Inflammasomes are large intracellular multiprotein complexes that play a central role in innate immunity by activating the release of proinflammatory cytokines. Although inflammasome activation has previously been linked to periodontal inflammation, there is still no information on a potential association with peri‐implantitis. The aim of this study was to examine cytotoxic and proinflammatory effects, including inflammasome activation, of metals used in dental implants, in an in vitro model, as well as from clinical tissue samples. MATERIAL AND METHODS: Human macrophages were exposed to different metals [titanium (Ti), cobalt, chromium and molybdenum] in a cell‐culture assay. Cytotoxicity was determined using the neutral red uptake assay. Cytokine secretion was quantified using an ELISA, and the expression of genes of various inflammasome components was analysed using quantitative PCR. In addition, the concentrations of interleukin‐1β (IL‐1β) and Ti in mucosal tissue samples taken in the vicinity of dental implants were determined using ELISA and inductively coupled plasma mass spectrometry, respectively. RESULTS: Ti ions in physiological solutions stimulated inflammasome activation in human macrophages and consequently IL‐1β release. This effect was further enhanced by macrophages that have been exposed to lipopolysaccharides. The proinflammatory activation caused by Ti ions disappeared after filtration (0.22 μm), which indicates an effect of particles. Ti ions alone did not stimulate transcription of the inflammasome components. The Ti levels of tissue samples obtained in the vicinity of Ti implants were sufficiently high (≥ 40 μm) to stimulate secretion of IL‐1β from human macrophages in vitro. CONCLUSION: Ti ions form particles that act as secondary stimuli for a proinflammatory reaction.
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spelling pubmed-52978752017-02-22 Titanium ions form particles that activate and execute interleukin‐1β release from lipopolysaccharide‐primed macrophages Pettersson, M. Kelk, P. Belibasakis, G. N. Bylund, D. Molin Thorén, M. Johansson, A. J Periodontal Res Original Articles BACKGROUND AND OBJECTIVE: Peri‐implantitis is a destructive inflammatory process characterized by destruction of the implant‐supporting bone. Inflammasomes are large intracellular multiprotein complexes that play a central role in innate immunity by activating the release of proinflammatory cytokines. Although inflammasome activation has previously been linked to periodontal inflammation, there is still no information on a potential association with peri‐implantitis. The aim of this study was to examine cytotoxic and proinflammatory effects, including inflammasome activation, of metals used in dental implants, in an in vitro model, as well as from clinical tissue samples. MATERIAL AND METHODS: Human macrophages were exposed to different metals [titanium (Ti), cobalt, chromium and molybdenum] in a cell‐culture assay. Cytotoxicity was determined using the neutral red uptake assay. Cytokine secretion was quantified using an ELISA, and the expression of genes of various inflammasome components was analysed using quantitative PCR. In addition, the concentrations of interleukin‐1β (IL‐1β) and Ti in mucosal tissue samples taken in the vicinity of dental implants were determined using ELISA and inductively coupled plasma mass spectrometry, respectively. RESULTS: Ti ions in physiological solutions stimulated inflammasome activation in human macrophages and consequently IL‐1β release. This effect was further enhanced by macrophages that have been exposed to lipopolysaccharides. The proinflammatory activation caused by Ti ions disappeared after filtration (0.22 μm), which indicates an effect of particles. Ti ions alone did not stimulate transcription of the inflammasome components. The Ti levels of tissue samples obtained in the vicinity of Ti implants were sufficiently high (≥ 40 μm) to stimulate secretion of IL‐1β from human macrophages in vitro. CONCLUSION: Ti ions form particles that act as secondary stimuli for a proinflammatory reaction. John Wiley and Sons Inc. 2016-03-14 2017-02 /pmc/articles/PMC5297875/ /pubmed/26987886 http://dx.doi.org/10.1111/jre.12364 Text en © 2016 The Authors. Journal of Periodontal Research published by John Wiley & Sons Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Pettersson, M.
Kelk, P.
Belibasakis, G. N.
Bylund, D.
Molin Thorén, M.
Johansson, A.
Titanium ions form particles that activate and execute interleukin‐1β release from lipopolysaccharide‐primed macrophages
title Titanium ions form particles that activate and execute interleukin‐1β release from lipopolysaccharide‐primed macrophages
title_full Titanium ions form particles that activate and execute interleukin‐1β release from lipopolysaccharide‐primed macrophages
title_fullStr Titanium ions form particles that activate and execute interleukin‐1β release from lipopolysaccharide‐primed macrophages
title_full_unstemmed Titanium ions form particles that activate and execute interleukin‐1β release from lipopolysaccharide‐primed macrophages
title_short Titanium ions form particles that activate and execute interleukin‐1β release from lipopolysaccharide‐primed macrophages
title_sort titanium ions form particles that activate and execute interleukin‐1β release from lipopolysaccharide‐primed macrophages
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5297875/
https://www.ncbi.nlm.nih.gov/pubmed/26987886
http://dx.doi.org/10.1111/jre.12364
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