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The Role of Mast Cells in IgE-Independent Lung Diseases

Mast cells (MCs) are granular cells of the innate immune system which develop from CD34(+)/CD117(+) progenitors and play a role in orchestrating adaptive immune responses. They have a well-known role in allergic reactions following immunoglobulin (Ig)E-mediated activation of the cell-surface express...

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Autores principales: Komi, Daniel Elieh Ali, Mortaz, Esmaeil, Amani, Saeede, Tiotiu, Angelica, Folkerts, Gert, Adcock, Ian M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244458/
https://www.ncbi.nlm.nih.gov/pubmed/32086776
http://dx.doi.org/10.1007/s12016-020-08779-5
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author Komi, Daniel Elieh Ali
Mortaz, Esmaeil
Amani, Saeede
Tiotiu, Angelica
Folkerts, Gert
Adcock, Ian M
author_facet Komi, Daniel Elieh Ali
Mortaz, Esmaeil
Amani, Saeede
Tiotiu, Angelica
Folkerts, Gert
Adcock, Ian M
author_sort Komi, Daniel Elieh Ali
collection PubMed
description Mast cells (MCs) are granular cells of the innate immune system which develop from CD34(+)/CD117(+) progenitors and play a role in orchestrating adaptive immune responses. They have a well-known role in allergic reactions following immunoglobulin (Ig)E-mediated activation of the cell-surface expressed IgE high-affinity receptor (FcεRI). MCs can also respond to various other stimuli due to the expression of a variety of receptors including toll-like receptors (TLRs), immunoglobulin (IgG) receptors (FcγR), complement receptors such as C5a (CD88) expressed by skin MCs, neuropeptides receptors including nerve growth factor receptor, (NGFR), cytokines receptors such as (IL)-1R and IL-3R, and chemokines receptors including CCR-1 and CCR-3. MCs release three groups of mediators upon degranulation differentiated according to their chemical composition, storage, and time to release. These include preformed mediators (mainly histamine, tryptase, and chymase), de novo synthesized mediators such as prostaglandin (PG)D2, leukotriene (LT)B4 and LTD4, and cytokines including IL-1β, IL-3, tumor necrosis factor (TNF)α, and transforming growth factor(TGF)-β. Emerging evidence indicates a role for IgE-independent MC activation in the late-stage asthmatic response as well as in non-allergic airway diseases including chronic obstructive pulmonary disease (COPD), idiopathic pulmonary fibrosis (IPF), and lung cancer. MC infiltration/activation has been reported in some, but not all, studies of lung cancer. MC-derived TNF-α possesses tumor-suppressive activity while IL-1β supports tumor progression and metastasis. In IPF lungs, an increase in density of tryptase- and chymase-positive MCs (MCTC) and overexpression of TGF-β support the fibrosis progression. MC-derived chymase activates latent TGF-β that induces the differentiation of fibroblasts to matrix-producing myofibroblasts. In summary, increasing evidence highlights a critical role of MCs in non-allergic diseases that may indicate new approaches for therapy.
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spelling pubmed-72444582020-06-03 The Role of Mast Cells in IgE-Independent Lung Diseases Komi, Daniel Elieh Ali Mortaz, Esmaeil Amani, Saeede Tiotiu, Angelica Folkerts, Gert Adcock, Ian M Clin Rev Allergy Immunol Article Mast cells (MCs) are granular cells of the innate immune system which develop from CD34(+)/CD117(+) progenitors and play a role in orchestrating adaptive immune responses. They have a well-known role in allergic reactions following immunoglobulin (Ig)E-mediated activation of the cell-surface expressed IgE high-affinity receptor (FcεRI). MCs can also respond to various other stimuli due to the expression of a variety of receptors including toll-like receptors (TLRs), immunoglobulin (IgG) receptors (FcγR), complement receptors such as C5a (CD88) expressed by skin MCs, neuropeptides receptors including nerve growth factor receptor, (NGFR), cytokines receptors such as (IL)-1R and IL-3R, and chemokines receptors including CCR-1 and CCR-3. MCs release three groups of mediators upon degranulation differentiated according to their chemical composition, storage, and time to release. These include preformed mediators (mainly histamine, tryptase, and chymase), de novo synthesized mediators such as prostaglandin (PG)D2, leukotriene (LT)B4 and LTD4, and cytokines including IL-1β, IL-3, tumor necrosis factor (TNF)α, and transforming growth factor(TGF)-β. Emerging evidence indicates a role for IgE-independent MC activation in the late-stage asthmatic response as well as in non-allergic airway diseases including chronic obstructive pulmonary disease (COPD), idiopathic pulmonary fibrosis (IPF), and lung cancer. MC infiltration/activation has been reported in some, but not all, studies of lung cancer. MC-derived TNF-α possesses tumor-suppressive activity while IL-1β supports tumor progression and metastasis. In IPF lungs, an increase in density of tryptase- and chymase-positive MCs (MCTC) and overexpression of TGF-β support the fibrosis progression. MC-derived chymase activates latent TGF-β that induces the differentiation of fibroblasts to matrix-producing myofibroblasts. In summary, increasing evidence highlights a critical role of MCs in non-allergic diseases that may indicate new approaches for therapy. Springer US 2020-02-21 2020 /pmc/articles/PMC7244458/ /pubmed/32086776 http://dx.doi.org/10.1007/s12016-020-08779-5 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Komi, Daniel Elieh Ali
Mortaz, Esmaeil
Amani, Saeede
Tiotiu, Angelica
Folkerts, Gert
Adcock, Ian M
The Role of Mast Cells in IgE-Independent Lung Diseases
title The Role of Mast Cells in IgE-Independent Lung Diseases
title_full The Role of Mast Cells in IgE-Independent Lung Diseases
title_fullStr The Role of Mast Cells in IgE-Independent Lung Diseases
title_full_unstemmed The Role of Mast Cells in IgE-Independent Lung Diseases
title_short The Role of Mast Cells in IgE-Independent Lung Diseases
title_sort role of mast cells in ige-independent lung diseases
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7244458/
https://www.ncbi.nlm.nih.gov/pubmed/32086776
http://dx.doi.org/10.1007/s12016-020-08779-5
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