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      The aryl hydrocarbon receptor pathway: a linking bridge between the gut microbiome and neurodegenerative diseases

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          Abstract

          The Aryl hydrocarbon receptor (AHR) is a cytosolic receptor and ligand-activated transcription factor widely expressed across various cell types in the body. Its signaling is vital for host responses at barrier sites, regulating epithelial renewal, barrier integrity, and the activities of several types of immune cells. This makes AHR essential for various cellular responses during aging, especially those governing inflammation and immunity. In this review, we provided an overview of the mechanisms by which the AHR mediates inflammatory response at gut and brain level through signals from intestinal microbes. The age-related reduction of gut microbiota functions is perceived as a trigger of aberrant immune responses linking gut and brain inflammation to neurodegeneration. Thus, we explored gut microbiome impact on the nature and availability of AHR ligands and outcomes for several signaling pathways involved in neurodegenerative diseases and age-associated decline of brain functions, with an insight on Parkinson’s and Alzheimer’s diseases, the most common neurodegenerative diseases in the elderly. Specifically, we focused on microbial tryptophan catabolism responsible for the production of several AHR ligands. Perspectives for the development of microbiota-based interventions targeting AHR activity are presented for a healthy aging.

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          Gut Microbiota Regulation of Tryptophan Metabolism in Health and Disease

          The gut microbiota is a crucial actor in human physiology. Many of these effects are mediated by metabolites that are either produced by the microbes or derived from the transformation of environmental or host molecules. Among the array of metabolites at the interface between these microorganisms and the host is the essential aromatic amino acid tryptophan (Trp). In the gut, the three major Trp metabolism pathways leading to serotonin (5-hydroxytryptamine), kynurenine (Kyn), and indole derivatives are under the direct or indirect control of the microbiota. In this review, we gather the most recent advances concerning the central role of Trp metabolism in microbiota-host crosstalk in health and disease. Deciphering the complex equilibrium between these pathways will facilitate a better understanding of the pathogenesis of human diseases and open therapeutic opportunities.
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            Gut microbiome alterations in Alzheimer’s disease

            Alzheimer’s disease (AD) is the most common form of dementia. However, the etiopathogenesis of this devastating disease is not fully understood. Recent studies in rodents suggest that alterations in the gut microbiome may contribute to amyloid deposition, yet the microbial communities associated with AD have not been characterized in humans. Towards this end, we characterized the bacterial taxonomic composition of fecal samples from participants with and without a diagnosis of dementia due to AD. Our analyses revealed that the gut microbiome of AD participants has decreased microbial diversity and is compositionally distinct from control age- and sex-matched individuals. We identified phylum- through genus-wide differences in bacterial abundance including decreased Firmicutes, increased Bacteroidetes, and decreased Bifidobacterium in the microbiome of AD participants. Furthermore, we observed correlations between levels of differentially abundant genera and cerebrospinal fluid (CSF) biomarkers of AD. These findings add AD to the growing list of diseases associated with gut microbial alterations, as well as suggest that gut bacterial communities may be a target for therapeutic intervention.
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              Tryptophan catabolites from microbiota engage aryl hydrocarbon receptor and balance mucosal reactivity via interleukin-22.

              Endogenous tryptophan (Trp) metabolites have an important role in mammalian gut immune homeostasis, yet the potential contribution of Trp metabolites from resident microbiota has never been addressed experimentally. Here, we describe a metabolic pathway whereby Trp metabolites from the microbiota balance mucosal reactivity in mice. Switching from sugar to Trp as an energy source (e.g., under conditions of unrestricted Trp availability), highly adaptive lactobacilli are expanded and produce an aryl hydrocarbon receptor (AhR) ligand-indole-3-aldehyde-that contributes to AhR-dependent Il22 transcription. The resulting IL-22-dependent balanced mucosal response allows for survival of mixed microbial communities yet provides colonization resistance to the fungus Candida albicans and mucosal protection from inflammation. Thus, the microbiota-AhR axis might represent an important strategy pursued by coevolutive commensalism for fine tuning host mucosal reactivity contingent on Trp catabolism. Copyright © 2013 Elsevier Inc. All rights reserved.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/593260/overviewRole:
                URI : https://loop.frontiersin.org/people/726011/overviewRole: Role:
                URI : https://loop.frontiersin.org/people/154681/overviewRole: Role:
                Journal
                Front Cell Neurosci
                Front Cell Neurosci
                Front. Cell. Neurosci.
                Frontiers in Cellular Neuroscience
                Frontiers Media S.A.
                1662-5102
                08 August 2024
                2024
                : 18
                : 1433747
                Affiliations
                [1] 1Department of Pharmacy, University of Naples Federico II , Naples, Italy
                [2] 2Task Force on Microbiome Studies, University of Naples Federico II , Naples, Italy
                Author notes

                Edited by: Hayet Sellami, University of Sfax, Tunisia

                Reviewed by: Dorra Abdelmalek, Centre of Biotechnology of Sfax, Tunisia

                Greta Volpedo, University of Genoa, Italy

                *Correspondence: Francesca Lembo, frlembo@ 123456unina.it
                Article
                10.3389/fncel.2024.1433747
                11338779
                39175504
                eb5a41b5-2491-4b32-8626-a229ee5d1372
                Copyright © 2024 Coretti, Buommino and Lembo.

                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.

                History
                : 16 May 2024
                : 31 July 2024
                Page count
                Figures: 2, Tables: 1, Equations: 0, References: 116, Pages: 12, Words: 11088
                Funding
                Funded by: #NEXTGENERATIONEU (NGEU) and funded by the Ministry of University and Research (MUR), NaEonal Recovery and Resilience Plan (NRRP)
                Award ID: PE0000006
                The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. This work was supported by #NEXTGENERATIONEU (NGEU) and funded by the Ministry of University and Research (MUR), NaEonal Recovery and Resilience Plan (NRRP), project MNESYS (PE0000006) – A MulEscale integrated approach to the study of the nervous system in health and disease [DN. 1553(DN. 11.10.2022) to LC].
                Categories
                Cellular Neuroscience
                Review
                Custom metadata
                Cellular Neuropathology

                Neurosciences
                microbiota-gut-brain axis,neuroinflammation,ahr,alzheimer’s disease,parkinson’s disease,tryptophan metabolism

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