A generic receptor protein and small fused-ring token appear separately from a nucleus cutaway and a short DNA double helix.
Receptor-context reconstruction Editorially reviewed

Human AHR cellular context. The separated teaching forms do not establish protein conformation, ligand binding, translocation, DNA interaction, transcription, pathway activity, exposure response, biomarker status, or diagnosis.

WikiBiome / Microbiome MedicineUniProt-human-AHR-identity and literal-output-audit-informed reconstruction
Scientific media record2 verified identifiers
Subject
Aryl Hydrocarbon Receptorbiological-process
Review
Editorial review completeIdentifiers authority-verified · Accessibility validated · · aryl-hydrocarbon-receptor|aryl-hydrocarbon-receptor-mechanism-v1.webp
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Trained-algorithmic mediaCreated with a trained generative algorithm and reviewed by WikiBiome for subject identity, scientific framing, identifiers, provenance, and accessibility.
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CC BY-SA 4.0Created

This page serves as a cross-reference point for the existing AhR (Aryl Hydrocarbon Receptor) concept page, which provides comprehensive coverage of AhR signaling, microbiome-derived ligands, and immune regulation.

The aryl hydrocarbon receptor is a ligand-activated transcription factor that integrates microbial, dietary, and environmental signals to regulate gut barrier integrity, immune tolerance, and Metal-Driven Inflammation.

Originally identified as a xenobiotic sensor (binding dioxins and polycyclic aromatic hydrocarbons), AhR is now recognized as a critical node in the microbiome-immune axis, where microbial tryptophan metabolites serve as its primary endogenous ligands.

For full coverage, see AhR (Aryl Hydrocarbon Receptor).

Contents1. Key Cross-References

Key Cross-References#

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References 8

Numbered by first appearance in the article, then reconciled with its declared source list.

  1. 1

    Natalia A. Borges, Amanda F. Barros, Lia S. Nakao et al. (2016). Protein-Bound Uremic Toxins from Gut Microbiota and Inflammatory Markers in CKD. Journal of Renal Nutrition.

  2. 2

    Friederike Gutmann, Lina Samira Bahr, Ulrike Bruning et al. (2025). Functional Microbiome Reprogramming Links Dietary Interventions to Neuroinflammatory Outcomes in Multiple Sclerosis. Research Square (preprint).

  3. 3

    Shokufeh Ghasemian Sorboni, Hanieh Shakeri Moghaddam, Reza Jafarzadeh-Esfehani et al. (2023). Ghasemian Sorboni 2023 — Comprehensive Review on Gut Microbiome in Neurological Disorders. Unknown.

  4. 4

    Various (2023). Metabolic Pathways 2023-2025 — Gut Microbiome Metabolic Activity in Type 1 Diabetes. Various.

  5. 5

    Allison M. Plummer, Yvette L. Matos, Henry C. Lin et al. (2023). Plummer et al 2023 — Gut-Brain Pathogenesis of Post-Acute COVID-19 Neurocognitive Symptoms. Frontiers in Neuroscience.

  6. 6

    Nicholas Dopkins, William Becker, Kathryn Miranda et al. (2021). Tryptamine Attenuates Experimental Multiple Sclerosis Through Activation of Aryl Hydrocarbon Receptor. Frontiers in Pharmacology.

  7. 7

    Benedetta Parodi, Nicole Kerlero de Rosbo (2021). The Gut-Brain Axis in Multiple Sclerosis. Is Its Dysfunction a Pathological Trigger or a Consequence of the Disease?. Frontiers in Immunology.

  8. 8

    Qing Zhang, Liqian Lu, Jiao Wang et al. (2024). Metabolomic Profiling Reveals Step-Wise Alteration of Bile Acid Metabolism in Diabetic Kidney Disease. Nutrition and Diabetes.

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