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Mast cells and mast cell tryptase enhance migration of human lung fibroblasts through protease-activated receptor 2
BACKGROUND: Mast cells may activate fibroblasts and contribute to remodeling processes in the lung. However, the mechanism behind these actions needs to be further investigated. Fibroblasts are major regulators of on-going remodeling processes. Protease activated receptor 2 (PAR2) expressed by fibro...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6139170/ https://www.ncbi.nlm.nih.gov/pubmed/30219079 http://dx.doi.org/10.1186/s12964-018-0269-3 |
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author | Bagher, Mariam Larsson-Callerfelt, Anna-Karin Rosmark, Oskar Hallgren, Oskar Bjermer, Leif Westergren-Thorsson, Gunilla |
author_facet | Bagher, Mariam Larsson-Callerfelt, Anna-Karin Rosmark, Oskar Hallgren, Oskar Bjermer, Leif Westergren-Thorsson, Gunilla |
author_sort | Bagher, Mariam |
collection | PubMed |
description | BACKGROUND: Mast cells may activate fibroblasts and contribute to remodeling processes in the lung. However, the mechanism behind these actions needs to be further investigated. Fibroblasts are major regulators of on-going remodeling processes. Protease activated receptor 2 (PAR2) expressed by fibroblasts may be activated by serine proteases, such as the mast cell mediator tryptase. The objective in this study was to investigate the effects of mast cells and specifically mast cell tryptase on fibroblast migration and the role of PAR2 activation. METHODS: Human lung fibroblasts (HFL-1) were cultured together with human peripheral blood-derived mast cells or LAD2 mast cells and stimulated with either conditioned medium from LAD2 cells or tryptase. Analyses of immunological stimulation of mast cells by IgE/anti IgE in the co-culture system were also performed. The importance of PAR2 activation by mast cells and mast cell tryptase for the migratory effects of fibroblasts was investigated by pre-treatment with the PAR2 antagonist P2pal-18S. The expression of PAR2 was analyzed on fibroblasts and mast cells. RESULTS: The migratory capacity of HFL-1 cells was enhanced by blood-derived mast cells (p < 0.02), LAD2 cells (p < 0.001), conditioned medium (p < 0.05) and tryptase (p < 0.006). P2pal-18S decreased the induced migration caused by mast cells (p < 0.001) and tryptase (p < 0.001) and the expression of PAR2 was verified in HFL-1 cells. Mast cells immunologically stimulated with IgE/Anti IgE had no further effects on fibroblast migration. CONCLUSIONS: Mast cells and the mast cell mediator tryptase may have crucial roles in inducing lung fibroblast migration via PAR-2 activation, which may contribute to remodeling processes in chronic lung diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12964-018-0269-3) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6139170 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-61391702018-09-20 Mast cells and mast cell tryptase enhance migration of human lung fibroblasts through protease-activated receptor 2 Bagher, Mariam Larsson-Callerfelt, Anna-Karin Rosmark, Oskar Hallgren, Oskar Bjermer, Leif Westergren-Thorsson, Gunilla Cell Commun Signal Research BACKGROUND: Mast cells may activate fibroblasts and contribute to remodeling processes in the lung. However, the mechanism behind these actions needs to be further investigated. Fibroblasts are major regulators of on-going remodeling processes. Protease activated receptor 2 (PAR2) expressed by fibroblasts may be activated by serine proteases, such as the mast cell mediator tryptase. The objective in this study was to investigate the effects of mast cells and specifically mast cell tryptase on fibroblast migration and the role of PAR2 activation. METHODS: Human lung fibroblasts (HFL-1) were cultured together with human peripheral blood-derived mast cells or LAD2 mast cells and stimulated with either conditioned medium from LAD2 cells or tryptase. Analyses of immunological stimulation of mast cells by IgE/anti IgE in the co-culture system were also performed. The importance of PAR2 activation by mast cells and mast cell tryptase for the migratory effects of fibroblasts was investigated by pre-treatment with the PAR2 antagonist P2pal-18S. The expression of PAR2 was analyzed on fibroblasts and mast cells. RESULTS: The migratory capacity of HFL-1 cells was enhanced by blood-derived mast cells (p < 0.02), LAD2 cells (p < 0.001), conditioned medium (p < 0.05) and tryptase (p < 0.006). P2pal-18S decreased the induced migration caused by mast cells (p < 0.001) and tryptase (p < 0.001) and the expression of PAR2 was verified in HFL-1 cells. Mast cells immunologically stimulated with IgE/Anti IgE had no further effects on fibroblast migration. CONCLUSIONS: Mast cells and the mast cell mediator tryptase may have crucial roles in inducing lung fibroblast migration via PAR-2 activation, which may contribute to remodeling processes in chronic lung diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12964-018-0269-3) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-15 /pmc/articles/PMC6139170/ /pubmed/30219079 http://dx.doi.org/10.1186/s12964-018-0269-3 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Bagher, Mariam Larsson-Callerfelt, Anna-Karin Rosmark, Oskar Hallgren, Oskar Bjermer, Leif Westergren-Thorsson, Gunilla Mast cells and mast cell tryptase enhance migration of human lung fibroblasts through protease-activated receptor 2 |
title | Mast cells and mast cell tryptase enhance migration of human lung fibroblasts through protease-activated receptor 2 |
title_full | Mast cells and mast cell tryptase enhance migration of human lung fibroblasts through protease-activated receptor 2 |
title_fullStr | Mast cells and mast cell tryptase enhance migration of human lung fibroblasts through protease-activated receptor 2 |
title_full_unstemmed | Mast cells and mast cell tryptase enhance migration of human lung fibroblasts through protease-activated receptor 2 |
title_short | Mast cells and mast cell tryptase enhance migration of human lung fibroblasts through protease-activated receptor 2 |
title_sort | mast cells and mast cell tryptase enhance migration of human lung fibroblasts through protease-activated receptor 2 |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6139170/ https://www.ncbi.nlm.nih.gov/pubmed/30219079 http://dx.doi.org/10.1186/s12964-018-0269-3 |
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