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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...

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Autores principales: Ding, Xiaomi, Zhou, Jing, Zhao, Li, Chen, Mingyue, Wang, Shenglin, Zhang, Ming, Zhang, Xiaodong, Jiang, Guohui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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.
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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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