Mast Cells Respond to Cell Injury through the Recognition of IL-33

Mast cells have been attributed several functions in both health and disease. Mast cell activation and release of inflammatory mediators are associated with the pathogenesis of several diseases, in particular that of allergic diseases. While the notion of mast cells as important, protective sentinel...

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Main Authors: Lunderius-Andersson, Carolina, Enoksson, Mattias, Nilsson, Gunnar
Format: Online
Language:English
Published: Frontiers Research Foundation 2012
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342375/
id pubmed-3342375
recordtype oai_dc
spelling pubmed-33423752012-05-07 Mast Cells Respond to Cell Injury through the Recognition of IL-33 Lunderius-Andersson, Carolina Enoksson, Mattias Nilsson, Gunnar Immunology Mast cells have been attributed several functions in both health and disease. Mast cell activation and release of inflammatory mediators are associated with the pathogenesis of several diseases, in particular that of allergic diseases. While the notion of mast cells as important, protective sentinel cells is old, this feature of the cell is not well recognized outside the mast cell field. The mast cell is a unique, multifunctional cell of our defense system, with characteristics such as wide-spread tissue distribution, expression of receptors capable of recognizing both endogenous and exogenous agents, and a capability to rapidly respond to triggering factors by selective mediator release. In this review, we discuss the function of mast cells as sentinel cells in the context of cell injury, where mast cells respond by initiating an inflammatory response. In this setting, IL-33 has turned out to be of particular interest. IL-33 is released by necrotic structural cells and is recognized by mast cells via the IL-33 receptor ST2. IL-33 and mast cells probably constitute one important link between cell injury and an inflammatory response that can lead to restoration of tissue function and homeostasis, but might under other circumstances contribute to a vicious circle driving chronic inflammation. Frontiers Research Foundation 2012-04-19 /pmc/articles/PMC3342375/ /pubmed/22566963 http://dx.doi.org/10.3389/fimmu.2012.00082 Text en Copyright © 2012 Lunderius-Andersson, Enoksson and Nilsson. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution Non Commercial License, which permits non-commercial use, distribution, and reproduction in other forums, provided the original authors and source are credited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Lunderius-Andersson, Carolina
Enoksson, Mattias
Nilsson, Gunnar
spellingShingle Lunderius-Andersson, Carolina
Enoksson, Mattias
Nilsson, Gunnar
Mast Cells Respond to Cell Injury through the Recognition of IL-33
author_facet Lunderius-Andersson, Carolina
Enoksson, Mattias
Nilsson, Gunnar
author_sort Lunderius-Andersson, Carolina
title Mast Cells Respond to Cell Injury through the Recognition of IL-33
title_short Mast Cells Respond to Cell Injury through the Recognition of IL-33
title_full Mast Cells Respond to Cell Injury through the Recognition of IL-33
title_fullStr Mast Cells Respond to Cell Injury through the Recognition of IL-33
title_full_unstemmed Mast Cells Respond to Cell Injury through the Recognition of IL-33
title_sort mast cells respond to cell injury through the recognition of il-33
description Mast cells have been attributed several functions in both health and disease. Mast cell activation and release of inflammatory mediators are associated with the pathogenesis of several diseases, in particular that of allergic diseases. While the notion of mast cells as important, protective sentinel cells is old, this feature of the cell is not well recognized outside the mast cell field. The mast cell is a unique, multifunctional cell of our defense system, with characteristics such as wide-spread tissue distribution, expression of receptors capable of recognizing both endogenous and exogenous agents, and a capability to rapidly respond to triggering factors by selective mediator release. In this review, we discuss the function of mast cells as sentinel cells in the context of cell injury, where mast cells respond by initiating an inflammatory response. In this setting, IL-33 has turned out to be of particular interest. IL-33 is released by necrotic structural cells and is recognized by mast cells via the IL-33 receptor ST2. IL-33 and mast cells probably constitute one important link between cell injury and an inflammatory response that can lead to restoration of tissue function and homeostasis, but might under other circumstances contribute to a vicious circle driving chronic inflammation.
publisher Frontiers Research Foundation
publishDate 2012
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3342375/
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