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Differential Regional Vulnerability of the Brain to Mild Neuroinflammation Induced by Systemic LPS Treatment in Mice

BACKGROUND: Peripheral inflammation-triggered mild neuroinflammation impacts the brain and behavior through microglial activation. In this study, we performed an unbiased analysis of the vulnerability of different brain areas to neuroinflammation induced by systemic inflammation. METHODS: We injecte...

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Autores principales: Jung, Hyeji, Lee, Hyojeong, Kim, Dongwook, Cheong, Eunji, Hyun, Young-Min, Yu, Je-Wook, Um, Ji Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140139/
https://www.ncbi.nlm.nih.gov/pubmed/35645573
http://dx.doi.org/10.2147/JIR.S362006
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author Jung, Hyeji
Lee, Hyojeong
Kim, Dongwook
Cheong, Eunji
Hyun, Young-Min
Yu, Je-Wook
Um, Ji Won
author_facet Jung, Hyeji
Lee, Hyojeong
Kim, Dongwook
Cheong, Eunji
Hyun, Young-Min
Yu, Je-Wook
Um, Ji Won
author_sort Jung, Hyeji
collection PubMed
description BACKGROUND: Peripheral inflammation-triggered mild neuroinflammation impacts the brain and behavior through microglial activation. In this study, we performed an unbiased analysis of the vulnerability of different brain areas to neuroinflammation induced by systemic inflammation. METHODS: We injected mice with a single low dose of LPS to induce mild inflammation and then analyzed microglial activation in 34 brain regions by immunohistochemical methods and whole-brain imaging using multi-slide scanning microscopy. We also conducted quantitative RT-PCR to measure the levels of inflammatory cytokines in selected brain regions of interest. RESULTS: We found that microglia in different brain regions are differentially activated by mild, LPS-induced inflammation relative to the increase in microglia numbers or increased CD68 expression. The increased number of microglia induced by mild inflammation was not attributable to infiltration of peripheral immune cells. In addition, microglia residing in brain regions, in which a single low-dose injection of LPS produced microglial changes, preferentially generated pro-inflammatory cytokines. CONCLUSION: Our results suggest that mild neuroinflammation induces regionally different microglia activation, producing pro-inflammatory cytokines. Our observations provide insight into induction of possible region-specific neuroinflammation-associated brain pathologies through microglial activation.
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spelling pubmed-91401392022-05-28 Differential Regional Vulnerability of the Brain to Mild Neuroinflammation Induced by Systemic LPS Treatment in Mice Jung, Hyeji Lee, Hyojeong Kim, Dongwook Cheong, Eunji Hyun, Young-Min Yu, Je-Wook Um, Ji Won J Inflamm Res Original Research BACKGROUND: Peripheral inflammation-triggered mild neuroinflammation impacts the brain and behavior through microglial activation. In this study, we performed an unbiased analysis of the vulnerability of different brain areas to neuroinflammation induced by systemic inflammation. METHODS: We injected mice with a single low dose of LPS to induce mild inflammation and then analyzed microglial activation in 34 brain regions by immunohistochemical methods and whole-brain imaging using multi-slide scanning microscopy. We also conducted quantitative RT-PCR to measure the levels of inflammatory cytokines in selected brain regions of interest. RESULTS: We found that microglia in different brain regions are differentially activated by mild, LPS-induced inflammation relative to the increase in microglia numbers or increased CD68 expression. The increased number of microglia induced by mild inflammation was not attributable to infiltration of peripheral immune cells. In addition, microglia residing in brain regions, in which a single low-dose injection of LPS produced microglial changes, preferentially generated pro-inflammatory cytokines. CONCLUSION: Our results suggest that mild neuroinflammation induces regionally different microglia activation, producing pro-inflammatory cytokines. Our observations provide insight into induction of possible region-specific neuroinflammation-associated brain pathologies through microglial activation. Dove 2022-05-23 /pmc/articles/PMC9140139/ /pubmed/35645573 http://dx.doi.org/10.2147/JIR.S362006 Text en © 2022 Jung et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Jung, Hyeji
Lee, Hyojeong
Kim, Dongwook
Cheong, Eunji
Hyun, Young-Min
Yu, Je-Wook
Um, Ji Won
Differential Regional Vulnerability of the Brain to Mild Neuroinflammation Induced by Systemic LPS Treatment in Mice
title Differential Regional Vulnerability of the Brain to Mild Neuroinflammation Induced by Systemic LPS Treatment in Mice
title_full Differential Regional Vulnerability of the Brain to Mild Neuroinflammation Induced by Systemic LPS Treatment in Mice
title_fullStr Differential Regional Vulnerability of the Brain to Mild Neuroinflammation Induced by Systemic LPS Treatment in Mice
title_full_unstemmed Differential Regional Vulnerability of the Brain to Mild Neuroinflammation Induced by Systemic LPS Treatment in Mice
title_short Differential Regional Vulnerability of the Brain to Mild Neuroinflammation Induced by Systemic LPS Treatment in Mice
title_sort differential regional vulnerability of the brain to mild neuroinflammation induced by systemic lps treatment in mice
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9140139/
https://www.ncbi.nlm.nih.gov/pubmed/35645573
http://dx.doi.org/10.2147/JIR.S362006
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