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Gut microbiota alterations affect glioma growth and innate immune cells involved in tumor immunosurveillance in mice
Glioma is a CNS tumor with few therapeutic options. Recently, host microbiota has been involved in the immune modulation of different tumors, but no data are available on the possible effects of the gut–immune axis on brain tumors. Here, we investigated the effect of gut microbiota alteration in a s...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216943/ https://www.ncbi.nlm.nih.gov/pubmed/32034922 http://dx.doi.org/10.1002/eji.201948354 |
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author | D'Alessandro, Giuseppina Antonangeli, Fabrizio Marrocco, Francesco Porzia, Alessandra Lauro, Clotilde Santoni, Angela Limatola, Cristina |
author_facet | D'Alessandro, Giuseppina Antonangeli, Fabrizio Marrocco, Francesco Porzia, Alessandra Lauro, Clotilde Santoni, Angela Limatola, Cristina |
author_sort | D'Alessandro, Giuseppina |
collection | PubMed |
description | Glioma is a CNS tumor with few therapeutic options. Recently, host microbiota has been involved in the immune modulation of different tumors, but no data are available on the possible effects of the gut–immune axis on brain tumors. Here, we investigated the effect of gut microbiota alteration in a syngeneic (GL261) mouse model of glioma, treating mice with two antibiotics (ABX) and evaluating the effects on tumor growth, microbe composition, natural killer (NK) cells and microglia phenotype. We report that ABX treatment (i) altered the intestinal microbiota at family level, (ii) reduced cytotoxic NK cell subsets, and (iii) altered the expression of inflammatory and homeostatic proteins in microglia. All these findings could contribute to the increased growth of intracranial glioma that was observed after ABX treatment. These results demonstrate that chronic ABX administration alters microbiota composition and contributes to modulate brain immune state paving the way to glioma growth. |
format | Online Article Text |
id | pubmed-7216943 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72169432020-05-13 Gut microbiota alterations affect glioma growth and innate immune cells involved in tumor immunosurveillance in mice D'Alessandro, Giuseppina Antonangeli, Fabrizio Marrocco, Francesco Porzia, Alessandra Lauro, Clotilde Santoni, Angela Limatola, Cristina Eur J Immunol Tumor immunology Glioma is a CNS tumor with few therapeutic options. Recently, host microbiota has been involved in the immune modulation of different tumors, but no data are available on the possible effects of the gut–immune axis on brain tumors. Here, we investigated the effect of gut microbiota alteration in a syngeneic (GL261) mouse model of glioma, treating mice with two antibiotics (ABX) and evaluating the effects on tumor growth, microbe composition, natural killer (NK) cells and microglia phenotype. We report that ABX treatment (i) altered the intestinal microbiota at family level, (ii) reduced cytotoxic NK cell subsets, and (iii) altered the expression of inflammatory and homeostatic proteins in microglia. All these findings could contribute to the increased growth of intracranial glioma that was observed after ABX treatment. These results demonstrate that chronic ABX administration alters microbiota composition and contributes to modulate brain immune state paving the way to glioma growth. John Wiley and Sons Inc. 2020-03-01 2020-05 /pmc/articles/PMC7216943/ /pubmed/32034922 http://dx.doi.org/10.1002/eji.201948354 Text en © 2020 The Authors. European Journal of Immunology published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Tumor immunology D'Alessandro, Giuseppina Antonangeli, Fabrizio Marrocco, Francesco Porzia, Alessandra Lauro, Clotilde Santoni, Angela Limatola, Cristina Gut microbiota alterations affect glioma growth and innate immune cells involved in tumor immunosurveillance in mice |
title | Gut microbiota alterations affect glioma growth and innate immune cells involved in tumor immunosurveillance in mice |
title_full | Gut microbiota alterations affect glioma growth and innate immune cells involved in tumor immunosurveillance in mice |
title_fullStr | Gut microbiota alterations affect glioma growth and innate immune cells involved in tumor immunosurveillance in mice |
title_full_unstemmed | Gut microbiota alterations affect glioma growth and innate immune cells involved in tumor immunosurveillance in mice |
title_short | Gut microbiota alterations affect glioma growth and innate immune cells involved in tumor immunosurveillance in mice |
title_sort | gut microbiota alterations affect glioma growth and innate immune cells involved in tumor immunosurveillance in mice |
topic | Tumor immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7216943/ https://www.ncbi.nlm.nih.gov/pubmed/32034922 http://dx.doi.org/10.1002/eji.201948354 |
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