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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...

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Autores principales: Westfall, Susan, Caracci, Francesca, Estill, Molly, Frolinger, Tal, Shen, Li, Pasinetti, Giulio M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
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.
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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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