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Systemic administration of β-glucan induces immune training in microglia
BACKGROUND: An innate immune memory response can manifest in two ways: immune training and immune tolerance, which refers to an enhanced or suppressed immune response to a second challenge, respectively. Exposing monocytes to moderate-to-high amounts of bacterial lipopolysaccharide (LPS) induces imm...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901224/ https://www.ncbi.nlm.nih.gov/pubmed/33618716 http://dx.doi.org/10.1186/s12974-021-02103-4 |
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author | Heng, Yang Zhang, Xiaoming Borggrewe, Malte van Weering, Hilmar R. J. Brummer, Maaike L. Nijboer, Tjalling W. Joosten, Leo A. B. Netea, Mihai G. Boddeke, Erik W. G. M. Laman, Jon D. Eggen, Bart J. L. |
author_facet | Heng, Yang Zhang, Xiaoming Borggrewe, Malte van Weering, Hilmar R. J. Brummer, Maaike L. Nijboer, Tjalling W. Joosten, Leo A. B. Netea, Mihai G. Boddeke, Erik W. G. M. Laman, Jon D. Eggen, Bart J. L. |
author_sort | Heng, Yang |
collection | PubMed |
description | BACKGROUND: An innate immune memory response can manifest in two ways: immune training and immune tolerance, which refers to an enhanced or suppressed immune response to a second challenge, respectively. Exposing monocytes to moderate-to-high amounts of bacterial lipopolysaccharide (LPS) induces immune tolerance, whereas fungal β-glucan (BG) induces immune training. In microglia, it has been shown that different LPS inocula in vivo can induce either immune training or tolerance. Few studies focused on impact of BG on microglia and were only performed in vitro. The aim of the current study was to determine whether BG activates and induces immune memory in microglia upon peripheral administration in vivo. METHODS: Two experimental designs were used. In the acute design, mice received an intraperitoneal (i.p.) injection with PBS, 1 mg/kg LPS or 20 mg/kg BG and were terminated after 3 h, 1 or 2 days. In the preconditioning design, animals were first challenged i.p. with PBS, 1 mg/kg LPS or 20 mg/kg BG. After 2, 7 or 14 days, mice received a second injection with PBS or 1 mg/kg LPS and were sacrificed 3 h later. Microglia were isolated by fluorescence-activated cell sorting, and cytokine gene expression levels were determined. In addition, a self-developed program was used to analyze microglia morphological changes. Cytokine concentrations in serum were determined by a cytokine array. RESULTS: Microglia exhibited a classical inflammatory response to LPS, showing significant upregulation of Tnf, Il6, Il1β, Ccl2, Ccl3 and Csf1 expression, three h after injection, and obvious morphological changes 1 and 2 days after injection. With an interval of 2 days between two challenges, both BG and LPS induced immune training in microglia. The training effect of LPS changed into immune tolerance after a 7-day interval between 2 LPS challenges. Preconditioning with BG and LPS resulted in increased morphological changes in microglia in response to a systemic LPS challenge compared to naïve microglia. CONCLUSIONS: Our results demonstrate that preconditioning with BG and LPS both induced immune training of microglia at two days after the first challenge. However, with an interval of 7 days between the first and second challenge, LPS-preconditioning resulted in immune tolerance in microglia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-021-02103-4. |
format | Online Article Text |
id | pubmed-7901224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-79012242021-03-01 Systemic administration of β-glucan induces immune training in microglia Heng, Yang Zhang, Xiaoming Borggrewe, Malte van Weering, Hilmar R. J. Brummer, Maaike L. Nijboer, Tjalling W. Joosten, Leo A. B. Netea, Mihai G. Boddeke, Erik W. G. M. Laman, Jon D. Eggen, Bart J. L. J Neuroinflammation Research BACKGROUND: An innate immune memory response can manifest in two ways: immune training and immune tolerance, which refers to an enhanced or suppressed immune response to a second challenge, respectively. Exposing monocytes to moderate-to-high amounts of bacterial lipopolysaccharide (LPS) induces immune tolerance, whereas fungal β-glucan (BG) induces immune training. In microglia, it has been shown that different LPS inocula in vivo can induce either immune training or tolerance. Few studies focused on impact of BG on microglia and were only performed in vitro. The aim of the current study was to determine whether BG activates and induces immune memory in microglia upon peripheral administration in vivo. METHODS: Two experimental designs were used. In the acute design, mice received an intraperitoneal (i.p.) injection with PBS, 1 mg/kg LPS or 20 mg/kg BG and were terminated after 3 h, 1 or 2 days. In the preconditioning design, animals were first challenged i.p. with PBS, 1 mg/kg LPS or 20 mg/kg BG. After 2, 7 or 14 days, mice received a second injection with PBS or 1 mg/kg LPS and were sacrificed 3 h later. Microglia were isolated by fluorescence-activated cell sorting, and cytokine gene expression levels were determined. In addition, a self-developed program was used to analyze microglia morphological changes. Cytokine concentrations in serum were determined by a cytokine array. RESULTS: Microglia exhibited a classical inflammatory response to LPS, showing significant upregulation of Tnf, Il6, Il1β, Ccl2, Ccl3 and Csf1 expression, three h after injection, and obvious morphological changes 1 and 2 days after injection. With an interval of 2 days between two challenges, both BG and LPS induced immune training in microglia. The training effect of LPS changed into immune tolerance after a 7-day interval between 2 LPS challenges. Preconditioning with BG and LPS resulted in increased morphological changes in microglia in response to a systemic LPS challenge compared to naïve microglia. CONCLUSIONS: Our results demonstrate that preconditioning with BG and LPS both induced immune training of microglia at two days after the first challenge. However, with an interval of 7 days between the first and second challenge, LPS-preconditioning resulted in immune tolerance in microglia. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12974-021-02103-4. BioMed Central 2021-02-22 /pmc/articles/PMC7901224/ /pubmed/33618716 http://dx.doi.org/10.1186/s12974-021-02103-4 Text en © The Author(s) 2021 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Heng, Yang Zhang, Xiaoming Borggrewe, Malte van Weering, Hilmar R. J. Brummer, Maaike L. Nijboer, Tjalling W. Joosten, Leo A. B. Netea, Mihai G. Boddeke, Erik W. G. M. Laman, Jon D. Eggen, Bart J. L. Systemic administration of β-glucan induces immune training in microglia |
title | Systemic administration of β-glucan induces immune training in microglia |
title_full | Systemic administration of β-glucan induces immune training in microglia |
title_fullStr | Systemic administration of β-glucan induces immune training in microglia |
title_full_unstemmed | Systemic administration of β-glucan induces immune training in microglia |
title_short | Systemic administration of β-glucan induces immune training in microglia |
title_sort | systemic administration of β-glucan induces immune training in microglia |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7901224/ https://www.ncbi.nlm.nih.gov/pubmed/33618716 http://dx.doi.org/10.1186/s12974-021-02103-4 |
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