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Activation of Eosinophils and Mast Cells in Functional Dyspepsia: an Ultrastructural Evaluation

We recently identified mucosal mast cell and eosinophil hyperplasia in association with a duodenal impaired barrier function in functional dyspepsia (FD). We aimed to further describe the implication of these immune cells by assessing their activation state at the ultrastructural level and by evalua...

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Autores principales: Vanheel, Hanne, Vicario, Maria, Boesmans, Werend, Vanuytsel, Tim, Salvo-Romero, Eloisa, Tack, Jan, Farré, Ricard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876347/
https://www.ncbi.nlm.nih.gov/pubmed/29599471
http://dx.doi.org/10.1038/s41598-018-23620-y
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author Vanheel, Hanne
Vicario, Maria
Boesmans, Werend
Vanuytsel, Tim
Salvo-Romero, Eloisa
Tack, Jan
Farré, Ricard
author_facet Vanheel, Hanne
Vicario, Maria
Boesmans, Werend
Vanuytsel, Tim
Salvo-Romero, Eloisa
Tack, Jan
Farré, Ricard
author_sort Vanheel, Hanne
collection PubMed
description We recently identified mucosal mast cell and eosinophil hyperplasia in association with a duodenal impaired barrier function in functional dyspepsia (FD). We aimed to further describe the implication of these immune cells by assessing their activation state at the ultrastructural level and by evaluating the association between impaired epithelial integrity and immune activation. Duodenal biopsies were obtained from 24 FD patients and 37 healthy controls. The ultrastructure of mast cells and eosinophils was analyzed by transmission electron microscopy. Transepithelial electrical resistance and paracellular permeability were measured to evaluate epithelial barrier function. The type of degranulation in eosinophils and mast cells was piecemeal. Eosinophils displayed higher degree of degranulation in FD patients than in controls (p < 0.0001). Quantification revealed a decreased granular density in eosinophils of FD patients (p < 0.0001). The degree of degranulation in mast cells was similar in both groups. However, a more heterogeneous profile was found in the FD group (p < 0.0001). No association between epithelial integrity and the number and activation state of mucosal eosinophils and mast cells was found. We demonstrated ultrastructural changes in degranulation state of eosinophils and mast cells, suggesting that eosinophil and mast cell activation play a role in the pathophysiology of FD.
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spelling pubmed-58763472018-04-02 Activation of Eosinophils and Mast Cells in Functional Dyspepsia: an Ultrastructural Evaluation Vanheel, Hanne Vicario, Maria Boesmans, Werend Vanuytsel, Tim Salvo-Romero, Eloisa Tack, Jan Farré, Ricard Sci Rep Article We recently identified mucosal mast cell and eosinophil hyperplasia in association with a duodenal impaired barrier function in functional dyspepsia (FD). We aimed to further describe the implication of these immune cells by assessing their activation state at the ultrastructural level and by evaluating the association between impaired epithelial integrity and immune activation. Duodenal biopsies were obtained from 24 FD patients and 37 healthy controls. The ultrastructure of mast cells and eosinophils was analyzed by transmission electron microscopy. Transepithelial electrical resistance and paracellular permeability were measured to evaluate epithelial barrier function. The type of degranulation in eosinophils and mast cells was piecemeal. Eosinophils displayed higher degree of degranulation in FD patients than in controls (p < 0.0001). Quantification revealed a decreased granular density in eosinophils of FD patients (p < 0.0001). The degree of degranulation in mast cells was similar in both groups. However, a more heterogeneous profile was found in the FD group (p < 0.0001). No association between epithelial integrity and the number and activation state of mucosal eosinophils and mast cells was found. We demonstrated ultrastructural changes in degranulation state of eosinophils and mast cells, suggesting that eosinophil and mast cell activation play a role in the pathophysiology of FD. Nature Publishing Group UK 2018-03-29 /pmc/articles/PMC5876347/ /pubmed/29599471 http://dx.doi.org/10.1038/s41598-018-23620-y Text en © The Author(s) 2018 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Vanheel, Hanne
Vicario, Maria
Boesmans, Werend
Vanuytsel, Tim
Salvo-Romero, Eloisa
Tack, Jan
Farré, Ricard
Activation of Eosinophils and Mast Cells in Functional Dyspepsia: an Ultrastructural Evaluation
title Activation of Eosinophils and Mast Cells in Functional Dyspepsia: an Ultrastructural Evaluation
title_full Activation of Eosinophils and Mast Cells in Functional Dyspepsia: an Ultrastructural Evaluation
title_fullStr Activation of Eosinophils and Mast Cells in Functional Dyspepsia: an Ultrastructural Evaluation
title_full_unstemmed Activation of Eosinophils and Mast Cells in Functional Dyspepsia: an Ultrastructural Evaluation
title_short Activation of Eosinophils and Mast Cells in Functional Dyspepsia: an Ultrastructural Evaluation
title_sort activation of eosinophils and mast cells in functional dyspepsia: an ultrastructural evaluation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876347/
https://www.ncbi.nlm.nih.gov/pubmed/29599471
http://dx.doi.org/10.1038/s41598-018-23620-y
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