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Sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress
BACKGROUND: Biological sex plays a prominent role in the prevalence and severity of a number of important stress-related gastrointestinal and immune-related diseases including IBS and allergy/anaphylaxis. Despite the establishment of sex differences in these diseases, the underlying mechanisms contr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120457/ https://www.ncbi.nlm.nih.gov/pubmed/27895892 http://dx.doi.org/10.1186/s13293-016-0113-7 |
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author | Mackey, Emily Ayyadurai, Saravanan Pohl, Calvin S. D’ Costa, Susan Li, Yihang Moeser, Adam J. |
author_facet | Mackey, Emily Ayyadurai, Saravanan Pohl, Calvin S. D’ Costa, Susan Li, Yihang Moeser, Adam J. |
author_sort | Mackey, Emily |
collection | PubMed |
description | BACKGROUND: Biological sex plays a prominent role in the prevalence and severity of a number of important stress-related gastrointestinal and immune-related diseases including IBS and allergy/anaphylaxis. Despite the establishment of sex differences in these diseases, the underlying mechanisms contributing to sex differences remain poorly understood. The objective of this study was to define the role of biological sex on mast cells (MCs), an innate immune cell central to the pathophysiology of many GI and allergic disorders. METHODS: Twelve-week-old C57BL/6 male and female mice were exposed to immunological stress (2 h of IgE-mediated passive systemic anaphylaxis (PSA)) or psychological stress (1 h of restraint stress (RS)) and temperature, clinical scores, serum histamine, and intestinal permeability (for RS) were measured. Primary bone marrow-derived MCs (BMMCs) were harvested from male and female mice and analyzed for MC degranulation, signaling pathways, mediator content, and RNA transcriptome analysis. RESULTS: Sexually dimorphic responses were observed in both models of PSA and RS and in primary MCs. Compared with male mice, female mice exhibited increased clinical scores, hypothermia, and serum histamine levels in response to PSA and had greater intestinal permeability and serum histamine responses to RS. Primary BMMCs from female mice exhibited increased release of β-hexosaminidase, histamine, tryptase, and TNF-α upon stimulation with IgE/DNP and A23187. Increased mediator release in female BMMCs was not associated with increased upstream phospho-tyrosine signaling pathways or downstream Ca(2+) mobilization. Instead, increased mediator release in female MCs was associated with markedly increased capacity for synthesis and storage of MC granule-associated immune mediators as determined by MC mediator content and RNA transcriptome analysis. CONCLUSIONS: These results provide a new understanding of sexual dimorphic responses in MCs and have direct implications for stress-related diseases associated with a female predominance and MC hyperactivity including irritable bowel syndrome, allergy, and anaphylaxis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13293-016-0113-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5120457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-51204572016-11-28 Sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress Mackey, Emily Ayyadurai, Saravanan Pohl, Calvin S. D’ Costa, Susan Li, Yihang Moeser, Adam J. Biol Sex Differ Research BACKGROUND: Biological sex plays a prominent role in the prevalence and severity of a number of important stress-related gastrointestinal and immune-related diseases including IBS and allergy/anaphylaxis. Despite the establishment of sex differences in these diseases, the underlying mechanisms contributing to sex differences remain poorly understood. The objective of this study was to define the role of biological sex on mast cells (MCs), an innate immune cell central to the pathophysiology of many GI and allergic disorders. METHODS: Twelve-week-old C57BL/6 male and female mice were exposed to immunological stress (2 h of IgE-mediated passive systemic anaphylaxis (PSA)) or psychological stress (1 h of restraint stress (RS)) and temperature, clinical scores, serum histamine, and intestinal permeability (for RS) were measured. Primary bone marrow-derived MCs (BMMCs) were harvested from male and female mice and analyzed for MC degranulation, signaling pathways, mediator content, and RNA transcriptome analysis. RESULTS: Sexually dimorphic responses were observed in both models of PSA and RS and in primary MCs. Compared with male mice, female mice exhibited increased clinical scores, hypothermia, and serum histamine levels in response to PSA and had greater intestinal permeability and serum histamine responses to RS. Primary BMMCs from female mice exhibited increased release of β-hexosaminidase, histamine, tryptase, and TNF-α upon stimulation with IgE/DNP and A23187. Increased mediator release in female BMMCs was not associated with increased upstream phospho-tyrosine signaling pathways or downstream Ca(2+) mobilization. Instead, increased mediator release in female MCs was associated with markedly increased capacity for synthesis and storage of MC granule-associated immune mediators as determined by MC mediator content and RNA transcriptome analysis. CONCLUSIONS: These results provide a new understanding of sexual dimorphic responses in MCs and have direct implications for stress-related diseases associated with a female predominance and MC hyperactivity including irritable bowel syndrome, allergy, and anaphylaxis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13293-016-0113-7) contains supplementary material, which is available to authorized users. BioMed Central 2016-11-22 /pmc/articles/PMC5120457/ /pubmed/27895892 http://dx.doi.org/10.1186/s13293-016-0113-7 Text en © The Author(s). 2016 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 Mackey, Emily Ayyadurai, Saravanan Pohl, Calvin S. D’ Costa, Susan Li, Yihang Moeser, Adam J. Sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress |
title | Sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress |
title_full | Sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress |
title_fullStr | Sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress |
title_full_unstemmed | Sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress |
title_short | Sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress |
title_sort | sexual dimorphism in the mast cell transcriptome and the pathophysiological responses to immunological and psychological stress |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5120457/ https://www.ncbi.nlm.nih.gov/pubmed/27895892 http://dx.doi.org/10.1186/s13293-016-0113-7 |
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