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Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity
Chronic stress manifests as depressive- and anxiety-like behavior while recurrent stress elicits disproportionate behavioral impairments linked to stress-induced immunological priming. The gut-brain-microbiota-axis is a promising therapeutic target for stress-induced behavioral impairments as it sim...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264434/ https://www.ncbi.nlm.nih.gov/pubmed/34248950 http://dx.doi.org/10.3389/fimmu.2021.670500 |
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author | Westfall, Susan Caracci, Francesca Estill, Molly Frolinger, Tal Shen, Li Pasinetti, Giulio M. |
author_facet | Westfall, Susan Caracci, Francesca Estill, Molly Frolinger, Tal Shen, Li Pasinetti, Giulio M. |
author_sort | Westfall, Susan |
collection | PubMed |
description | Chronic stress manifests as depressive- and anxiety-like behavior while recurrent stress elicits disproportionate behavioral impairments linked to stress-induced immunological priming. The gut-brain-microbiota-axis is a promising therapeutic target for stress-induced behavioral impairments as it simultaneously modulates peripheral and brain immunological landscapes. In this study, a combination of probiotics and prebiotics, known as a synbiotic, promoted behavioral resilience to chronic and recurrent stress by normalizing gut microbiota populations and promoting regulatory T cell (Treg) expansion through modulation of ileal innate lymphoid cell (ILC)3 activity, an impact reflecting behavioral responses better than limbic brain region neuroinflammation. Supporting this conclusion, a multivariate machine learning model correlatively predicted a cross-tissue immunological signature of stress-induced behavioral impairment where the ileal Treg/T helper17 cell ratio associated to hippocampal chemotactic chemokine and prefrontal cortex IL-1β production in the context of stress-induced behavioral deficits. In conclusion, stress-induced behavioral impairments depend on the gut-brain-microbiota-axis and through ileal immune regulation, synbiotics attenuate the associated depressive- and anxiety-like behavior. |
format | Online Article Text |
id | pubmed-8264434 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82644342021-07-09 Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity Westfall, Susan Caracci, Francesca Estill, Molly Frolinger, Tal Shen, Li Pasinetti, Giulio M. Front Immunol Immunology Chronic stress manifests as depressive- and anxiety-like behavior while recurrent stress elicits disproportionate behavioral impairments linked to stress-induced immunological priming. The gut-brain-microbiota-axis is a promising therapeutic target for stress-induced behavioral impairments as it simultaneously modulates peripheral and brain immunological landscapes. In this study, a combination of probiotics and prebiotics, known as a synbiotic, promoted behavioral resilience to chronic and recurrent stress by normalizing gut microbiota populations and promoting regulatory T cell (Treg) expansion through modulation of ileal innate lymphoid cell (ILC)3 activity, an impact reflecting behavioral responses better than limbic brain region neuroinflammation. Supporting this conclusion, a multivariate machine learning model correlatively predicted a cross-tissue immunological signature of stress-induced behavioral impairment where the ileal Treg/T helper17 cell ratio associated to hippocampal chemotactic chemokine and prefrontal cortex IL-1β production in the context of stress-induced behavioral deficits. In conclusion, stress-induced behavioral impairments depend on the gut-brain-microbiota-axis and through ileal immune regulation, synbiotics attenuate the associated depressive- and anxiety-like behavior. Frontiers Media S.A. 2021-06-24 /pmc/articles/PMC8264434/ /pubmed/34248950 http://dx.doi.org/10.3389/fimmu.2021.670500 Text en Copyright © 2021 Westfall, Caracci, Estill, Frolinger, Shen and Pasinetti 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 | Immunology Westfall, Susan Caracci, Francesca Estill, Molly Frolinger, Tal Shen, Li Pasinetti, Giulio M. Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity |
title | Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity |
title_full | Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity |
title_fullStr | Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity |
title_full_unstemmed | Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity |
title_short | Chronic Stress-Induced Depression and Anxiety Priming Modulated by Gut-Brain-Axis Immunity |
title_sort | chronic stress-induced depression and anxiety priming modulated by gut-brain-axis immunity |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8264434/ https://www.ncbi.nlm.nih.gov/pubmed/34248950 http://dx.doi.org/10.3389/fimmu.2021.670500 |
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