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Serglycin proteoglycans limit enteropathy in Trichinella spiralis-infected mice
BACKGROUND: Serglycin proteoglycans are essential for maturation of secretory granules and for the correct granular storage of cationic proteases in hematopoietic cells, e.g. mast cells. However, little is known about the in vivo functions of serglycin proteoglycans during infection. Here we investi...
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/PMC4897876/ https://www.ncbi.nlm.nih.gov/pubmed/27267469 http://dx.doi.org/10.1186/s12865-016-0155-y |
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author | Roy, Ananya Sawesi, Osama Pettersson, Ulrika Dagälv, Anders Kjellén, Lena Lundén, Anna Åbrink, Magnus |
author_facet | Roy, Ananya Sawesi, Osama Pettersson, Ulrika Dagälv, Anders Kjellén, Lena Lundén, Anna Åbrink, Magnus |
author_sort | Roy, Ananya |
collection | PubMed |
description | BACKGROUND: Serglycin proteoglycans are essential for maturation of secretory granules and for the correct granular storage of cationic proteases in hematopoietic cells, e.g. mast cells. However, little is known about the in vivo functions of serglycin proteoglycans during infection. Here we investigated the potential role of serglycin proteoglycans in host defense after infection with the nematode Trichinella spiralis. RESULTS: Twelve days post infection lack of serglycin proteoglycans caused significantly increased enteropathy. The serglycin-deficient mice showed significantly increased intestinal worm burden, reduced recruitment of mast cells to the intestinal crypts, decreased levels of the mast cell proteases MCPT5 and MCPT6 in intestinal tissue, decreased serum levels of TNF-α, IL-1β, IL-10 and IL-13, increased levels of IL-4 and total IgE in serum, and increased intestinal levels of the neutrophil markers myeloperoxidase and elastase, as compared to wild type mice. At five weeks post infection, increased larvae burden and inflammation were seen in the muscle tissue of the serglycin-deficient mice. CONCLUSIONS: Our results demonstrate that the serglycin-deficient mice were more susceptible to T. spiralis infection and displayed an unbalanced immune response compared to wild type mice. These findings point to an essential regulatory role of serglycin proteoglycans in immunity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12865-016-0155-y) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4897876 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-48978762016-06-09 Serglycin proteoglycans limit enteropathy in Trichinella spiralis-infected mice Roy, Ananya Sawesi, Osama Pettersson, Ulrika Dagälv, Anders Kjellén, Lena Lundén, Anna Åbrink, Magnus BMC Immunol Research Article BACKGROUND: Serglycin proteoglycans are essential for maturation of secretory granules and for the correct granular storage of cationic proteases in hematopoietic cells, e.g. mast cells. However, little is known about the in vivo functions of serglycin proteoglycans during infection. Here we investigated the potential role of serglycin proteoglycans in host defense after infection with the nematode Trichinella spiralis. RESULTS: Twelve days post infection lack of serglycin proteoglycans caused significantly increased enteropathy. The serglycin-deficient mice showed significantly increased intestinal worm burden, reduced recruitment of mast cells to the intestinal crypts, decreased levels of the mast cell proteases MCPT5 and MCPT6 in intestinal tissue, decreased serum levels of TNF-α, IL-1β, IL-10 and IL-13, increased levels of IL-4 and total IgE in serum, and increased intestinal levels of the neutrophil markers myeloperoxidase and elastase, as compared to wild type mice. At five weeks post infection, increased larvae burden and inflammation were seen in the muscle tissue of the serglycin-deficient mice. CONCLUSIONS: Our results demonstrate that the serglycin-deficient mice were more susceptible to T. spiralis infection and displayed an unbalanced immune response compared to wild type mice. These findings point to an essential regulatory role of serglycin proteoglycans in immunity. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12865-016-0155-y) contains supplementary material, which is available to authorized users. BioMed Central 2016-06-08 /pmc/articles/PMC4897876/ /pubmed/27267469 http://dx.doi.org/10.1186/s12865-016-0155-y 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 Article Roy, Ananya Sawesi, Osama Pettersson, Ulrika Dagälv, Anders Kjellén, Lena Lundén, Anna Åbrink, Magnus Serglycin proteoglycans limit enteropathy in Trichinella spiralis-infected mice |
title | Serglycin proteoglycans limit enteropathy in Trichinella spiralis-infected mice |
title_full | Serglycin proteoglycans limit enteropathy in Trichinella spiralis-infected mice |
title_fullStr | Serglycin proteoglycans limit enteropathy in Trichinella spiralis-infected mice |
title_full_unstemmed | Serglycin proteoglycans limit enteropathy in Trichinella spiralis-infected mice |
title_short | Serglycin proteoglycans limit enteropathy in Trichinella spiralis-infected mice |
title_sort | serglycin proteoglycans limit enteropathy in trichinella spiralis-infected mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4897876/ https://www.ncbi.nlm.nih.gov/pubmed/27267469 http://dx.doi.org/10.1186/s12865-016-0155-y |
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