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Alterations in circulating extracellular vesicles underlie social stress‐induced behaviors in mice

Chronic stress induces peripheral and intracerebral immune changes and inflammation, contributing to neuropathology and behavioral abnormalities relevant to psychiatric disorders such as depression. Although the pathological implication of many peripheral factors such as pro‐inflammatory cytokines,...

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Autores principales: Sakamoto, Shinji, Mallah, Dania, Medeiros, Destynie J., Dohi, Eisuke, Imai, Takashi, Rose, Indigo V. L., Matoba, Ken, Zhu, Xiaolei, Kamiya, Atsushi, Kano, Shin‐ichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487053/
https://www.ncbi.nlm.nih.gov/pubmed/34043886
http://dx.doi.org/10.1002/2211-5463.13204
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author Sakamoto, Shinji
Mallah, Dania
Medeiros, Destynie J.
Dohi, Eisuke
Imai, Takashi
Rose, Indigo V. L.
Matoba, Ken
Zhu, Xiaolei
Kamiya, Atsushi
Kano, Shin‐ichi
author_facet Sakamoto, Shinji
Mallah, Dania
Medeiros, Destynie J.
Dohi, Eisuke
Imai, Takashi
Rose, Indigo V. L.
Matoba, Ken
Zhu, Xiaolei
Kamiya, Atsushi
Kano, Shin‐ichi
author_sort Sakamoto, Shinji
collection PubMed
description Chronic stress induces peripheral and intracerebral immune changes and inflammation, contributing to neuropathology and behavioral abnormalities relevant to psychiatric disorders such as depression. Although the pathological implication of many peripheral factors such as pro‐inflammatory cytokines, hormones, and macrophages has been demonstrated, the roles of circulating extracellular vesicles (EVs) for chronic stress mechanisms remain poorly investigated. Here, we report that chronic social defeat stress (CSDS)‐induced social avoidance phenotype, assessed by a previously untested three‐chamber social approach test, can be distinguished by multiple pro‐inflammatory cytokines and EV‐associated molecular signatures in the blood. We found that the expression patterns of miRNAs distinguished the CSDS‐susceptible mice from the CSDS‐resilient mice. Social avoidance behavior scores were also estimated with good accuracy by the expression patterns of multiple EV‐associated miRNAs. We also demonstrated that EVs enriched from the CSDS‐susceptible mouse sera upregulated the production of pro‐inflammatory cytokines in the LPS‐stimulated microglia‐like cell lines. Our results indicate the role of circulating EVs and associated miRNAs in CSDS susceptibility, which may be related to pro‐inflammatory mechanisms underlying stress‐induced neurobehavioral outcomes.
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spelling pubmed-84870532021-10-07 Alterations in circulating extracellular vesicles underlie social stress‐induced behaviors in mice Sakamoto, Shinji Mallah, Dania Medeiros, Destynie J. Dohi, Eisuke Imai, Takashi Rose, Indigo V. L. Matoba, Ken Zhu, Xiaolei Kamiya, Atsushi Kano, Shin‐ichi FEBS Open Bio Research Articles Chronic stress induces peripheral and intracerebral immune changes and inflammation, contributing to neuropathology and behavioral abnormalities relevant to psychiatric disorders such as depression. Although the pathological implication of many peripheral factors such as pro‐inflammatory cytokines, hormones, and macrophages has been demonstrated, the roles of circulating extracellular vesicles (EVs) for chronic stress mechanisms remain poorly investigated. Here, we report that chronic social defeat stress (CSDS)‐induced social avoidance phenotype, assessed by a previously untested three‐chamber social approach test, can be distinguished by multiple pro‐inflammatory cytokines and EV‐associated molecular signatures in the blood. We found that the expression patterns of miRNAs distinguished the CSDS‐susceptible mice from the CSDS‐resilient mice. Social avoidance behavior scores were also estimated with good accuracy by the expression patterns of multiple EV‐associated miRNAs. We also demonstrated that EVs enriched from the CSDS‐susceptible mouse sera upregulated the production of pro‐inflammatory cytokines in the LPS‐stimulated microglia‐like cell lines. Our results indicate the role of circulating EVs and associated miRNAs in CSDS susceptibility, which may be related to pro‐inflammatory mechanisms underlying stress‐induced neurobehavioral outcomes. John Wiley and Sons Inc. 2021-06-24 /pmc/articles/PMC8487053/ /pubmed/34043886 http://dx.doi.org/10.1002/2211-5463.13204 Text en © 2021 The Authors. FEBS Open Bio published by John Wiley & Sons Ltd on behalf of Federation of European Biochemical Societies https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Sakamoto, Shinji
Mallah, Dania
Medeiros, Destynie J.
Dohi, Eisuke
Imai, Takashi
Rose, Indigo V. L.
Matoba, Ken
Zhu, Xiaolei
Kamiya, Atsushi
Kano, Shin‐ichi
Alterations in circulating extracellular vesicles underlie social stress‐induced behaviors in mice
title Alterations in circulating extracellular vesicles underlie social stress‐induced behaviors in mice
title_full Alterations in circulating extracellular vesicles underlie social stress‐induced behaviors in mice
title_fullStr Alterations in circulating extracellular vesicles underlie social stress‐induced behaviors in mice
title_full_unstemmed Alterations in circulating extracellular vesicles underlie social stress‐induced behaviors in mice
title_short Alterations in circulating extracellular vesicles underlie social stress‐induced behaviors in mice
title_sort alterations in circulating extracellular vesicles underlie social stress‐induced behaviors in mice
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8487053/
https://www.ncbi.nlm.nih.gov/pubmed/34043886
http://dx.doi.org/10.1002/2211-5463.13204
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