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Intestinal Flora Composition Determines Microglia Activation and Improves Epileptic Episode Progress
In response to environmental stimuli, immune memory mediates the plasticity of myeloid cells. Immune training and immune tolerance are two aspects of plasticity. Microglia that are immunologically trained or immunologically tolerant are endowed with a tendency to differentiate into alternative domin...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959590/ https://www.ncbi.nlm.nih.gov/pubmed/35356535 http://dx.doi.org/10.3389/fcimb.2022.835217 |
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author | Ding, Xiaomi Zhou, Jing Zhao, Li Chen, Mingyue Wang, Shenglin Zhang, Ming Zhang, Xiaodong Jiang, Guohui |
author_facet | Ding, Xiaomi Zhou, Jing Zhao, Li Chen, Mingyue Wang, Shenglin Zhang, Ming Zhang, Xiaodong Jiang, Guohui |
author_sort | Ding, Xiaomi |
collection | PubMed |
description | In response to environmental stimuli, immune memory mediates the plasticity of myeloid cells. Immune training and immune tolerance are two aspects of plasticity. Microglia that are immunologically trained or immunologically tolerant are endowed with a tendency to differentiate into alternative dominant phenotypes (M1/M2). Male C57BL/6 mice (immune-training group, immune-tolerant group, and control group) were used to establish the kainic acid epilepsy model. The seizure grade, duration, latency, hippocampal potential, and energy density were used to evaluate seizures, and the changes in the polarization of microglia were detected by western blot. 16S rDNA sequencing showed that the abundance of Ruminococcus in the immune-tolerant group was the dominant flora. Our research connections Intestinal microorganisms, brain immune status, and epilepsy behavior together. Pro-inflammatory M1 phenotype and anti-inflammatory M2 phenotype mediate and enhance and suppress subsequent inflammation, respectively. We conclude that intestinal microorganisms influence the occurrence and development of epilepsy by regulating the polarization of microglia. |
format | Online Article Text |
id | pubmed-8959590 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-89595902022-03-29 Intestinal Flora Composition Determines Microglia Activation and Improves Epileptic Episode Progress Ding, Xiaomi Zhou, Jing Zhao, Li Chen, Mingyue Wang, Shenglin Zhang, Ming Zhang, Xiaodong Jiang, Guohui Front Cell Infect Microbiol Cellular and Infection Microbiology In response to environmental stimuli, immune memory mediates the plasticity of myeloid cells. Immune training and immune tolerance are two aspects of plasticity. Microglia that are immunologically trained or immunologically tolerant are endowed with a tendency to differentiate into alternative dominant phenotypes (M1/M2). Male C57BL/6 mice (immune-training group, immune-tolerant group, and control group) were used to establish the kainic acid epilepsy model. The seizure grade, duration, latency, hippocampal potential, and energy density were used to evaluate seizures, and the changes in the polarization of microglia were detected by western blot. 16S rDNA sequencing showed that the abundance of Ruminococcus in the immune-tolerant group was the dominant flora. Our research connections Intestinal microorganisms, brain immune status, and epilepsy behavior together. Pro-inflammatory M1 phenotype and anti-inflammatory M2 phenotype mediate and enhance and suppress subsequent inflammation, respectively. We conclude that intestinal microorganisms influence the occurrence and development of epilepsy by regulating the polarization of microglia. Frontiers Media S.A. 2022-03-09 /pmc/articles/PMC8959590/ /pubmed/35356535 http://dx.doi.org/10.3389/fcimb.2022.835217 Text en Copyright © 2022 Ding, Zhou, Zhao, Chen, Wang, Zhang, Zhang and Jiang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular and Infection Microbiology Ding, Xiaomi Zhou, Jing Zhao, Li Chen, Mingyue Wang, Shenglin Zhang, Ming Zhang, Xiaodong Jiang, Guohui Intestinal Flora Composition Determines Microglia Activation and Improves Epileptic Episode Progress |
title | Intestinal Flora Composition Determines Microglia Activation and Improves Epileptic Episode Progress |
title_full | Intestinal Flora Composition Determines Microglia Activation and Improves Epileptic Episode Progress |
title_fullStr | Intestinal Flora Composition Determines Microglia Activation and Improves Epileptic Episode Progress |
title_full_unstemmed | Intestinal Flora Composition Determines Microglia Activation and Improves Epileptic Episode Progress |
title_short | Intestinal Flora Composition Determines Microglia Activation and Improves Epileptic Episode Progress |
title_sort | intestinal flora composition determines microglia activation and improves epileptic episode progress |
topic | Cellular and Infection Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8959590/ https://www.ncbi.nlm.nih.gov/pubmed/35356535 http://dx.doi.org/10.3389/fcimb.2022.835217 |
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