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Effects of the Th2-dominant milieu on allergic responses in Der f 1-activated mouse basophils and mast cells
Although basophils and mast cells share similar phenotypic and functional properties, little is known about the difference in the initial Th2 immune responses of these cells following exposure to proteolytic allergens. Here, we investigated the mechanisms of Th2-mediated immune responses in mouse bo...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955989/ https://www.ncbi.nlm.nih.gov/pubmed/29769546 http://dx.doi.org/10.1038/s41598-018-25741-w |
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author | Yi, Myung-hee Kim, Hyoung-Pyo Jeong, Kyoung Yong Kim, Ju Yeong Lee, In-Yong Yong, Tai-Soon |
author_facet | Yi, Myung-hee Kim, Hyoung-Pyo Jeong, Kyoung Yong Kim, Ju Yeong Lee, In-Yong Yong, Tai-Soon |
author_sort | Yi, Myung-hee |
collection | PubMed |
description | Although basophils and mast cells share similar phenotypic and functional properties, little is known about the difference in the initial Th2 immune responses of these cells following exposure to proteolytic allergens. Here, we investigated the mechanisms of Th2-mediated immune responses in mouse bone marrow-derived basophils (BMBs) and mast cells (BMMCs) via stimulation with the cysteine protease allergen Der f 1. Our results showed that Th2 cytokines were induced from BMBs by active recombinant Der f 1 (rDer f 1 independently with Toll-like receptor (TLR) 2 and TLR4. Although both BMBs and BMMCs expressed protease-activated receptors on their surfaces, PAR expression following exposure to rDer f 1 was altered only in basophils. G protein-coupled receptors in basophils were found to be associated with interleukin (IL)-4 and IL-13 production from BMBs upon Der f 1 treatment. Secretion of Th2 cytokines from rDer f 1-treated basophils was mediated by G protein βγ and phosphatidylinositol 3-kinase γ through the extracellular signal-regulated kinase and c-Jun N-terminal kinase pathways. These findings provide insights into the roles of cysteine proteases in Th2 immune responses, such as allergic diseases, and improve our understanding of the mechanisms of Th2 cytokine production. |
format | Online Article Text |
id | pubmed-5955989 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59559892018-05-21 Effects of the Th2-dominant milieu on allergic responses in Der f 1-activated mouse basophils and mast cells Yi, Myung-hee Kim, Hyoung-Pyo Jeong, Kyoung Yong Kim, Ju Yeong Lee, In-Yong Yong, Tai-Soon Sci Rep Article Although basophils and mast cells share similar phenotypic and functional properties, little is known about the difference in the initial Th2 immune responses of these cells following exposure to proteolytic allergens. Here, we investigated the mechanisms of Th2-mediated immune responses in mouse bone marrow-derived basophils (BMBs) and mast cells (BMMCs) via stimulation with the cysteine protease allergen Der f 1. Our results showed that Th2 cytokines were induced from BMBs by active recombinant Der f 1 (rDer f 1 independently with Toll-like receptor (TLR) 2 and TLR4. Although both BMBs and BMMCs expressed protease-activated receptors on their surfaces, PAR expression following exposure to rDer f 1 was altered only in basophils. G protein-coupled receptors in basophils were found to be associated with interleukin (IL)-4 and IL-13 production from BMBs upon Der f 1 treatment. Secretion of Th2 cytokines from rDer f 1-treated basophils was mediated by G protein βγ and phosphatidylinositol 3-kinase γ through the extracellular signal-regulated kinase and c-Jun N-terminal kinase pathways. These findings provide insights into the roles of cysteine proteases in Th2 immune responses, such as allergic diseases, and improve our understanding of the mechanisms of Th2 cytokine production. Nature Publishing Group UK 2018-05-16 /pmc/articles/PMC5955989/ /pubmed/29769546 http://dx.doi.org/10.1038/s41598-018-25741-w 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 Yi, Myung-hee Kim, Hyoung-Pyo Jeong, Kyoung Yong Kim, Ju Yeong Lee, In-Yong Yong, Tai-Soon Effects of the Th2-dominant milieu on allergic responses in Der f 1-activated mouse basophils and mast cells |
title | Effects of the Th2-dominant milieu on allergic responses in Der f 1-activated mouse basophils and mast cells |
title_full | Effects of the Th2-dominant milieu on allergic responses in Der f 1-activated mouse basophils and mast cells |
title_fullStr | Effects of the Th2-dominant milieu on allergic responses in Der f 1-activated mouse basophils and mast cells |
title_full_unstemmed | Effects of the Th2-dominant milieu on allergic responses in Der f 1-activated mouse basophils and mast cells |
title_short | Effects of the Th2-dominant milieu on allergic responses in Der f 1-activated mouse basophils and mast cells |
title_sort | effects of the th2-dominant milieu on allergic responses in der f 1-activated mouse basophils and mast cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5955989/ https://www.ncbi.nlm.nih.gov/pubmed/29769546 http://dx.doi.org/10.1038/s41598-018-25741-w |
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