Glycine conjugates of indole-3-carboxylates are aryl hydrocarbon receptor ligands

Substituted indoles are conserved metabolites across all kingdoms of life and may function as a mediators of inter- and intra-species communication. Indole-3-carboxylates (indole-3-acetic acid (IAA) and indole-3-propionic acid (IPA)) represent abundant tryptophan-derived aryl hydrocarbon receptor (AHR) agonists in human serum, potentially influencing AHR-dependent physiology. LC-MS analysis of mouse serum, urine and cecal/fecal contents reveals that both IAA and IPA undergo host and microbial mediated glycine conjugation to facilitate urinary elimination. Notably, at physiologically detectable human serum concentrations (μM), IAA-Glycine retains human AHR activation potential. Comparative in silico docking simulations corroborate IAA-Glycine as a direct ligand for the human AHR. In contrast to xenobiotic ligands such as TCDD and FICZ, the endogenous tryptophan metabolites examined here exhibited greater activation associated with human AHR relative to mouse AHR. These results underscore the role of microbial and host-derived amino acid conjugation in generating bioactive metabolites and position auxin chemistry within human physiology. Glycine conjugates of indole-3-acetic acid and indole-3-propionic acid made by the host and/or the microbiome are Ah receptor agonists.

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Journal
Communications Biology
Published
2026-09-15
DOI
https://doi.org/10.1038/s42003-026-10831-7
Primary Topic
Toxic Organic Pollutants Impact
Type
article
Field-Weighted Citation Impact
0.00

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article

Glycine conjugates of indole-3-carboxylates are aryl hydrocarbon receptor ligands

Imhoi Koo, Craig B. Marcus, Fuhua Hao, Seth T. Walk et al.
Communications Biology
Toxic Organic Pollutants Impact
article

Glycine conjugates of indole-3-carboxylates are aryl hydrocarbon receptor ligands

Imhoi Koo, Craig B. Marcus, Fuhua Hao, Seth T. Walk, Fangcong Dong, Shantu Amin, Iain A. Murray, Andrew J. Annalora, Krishne Gowda, Jordan E. Bisanz, Denise M. Coslo, Andrew D. Patterson, Reece Erickson, Gary H. Perdew, Ethan W. Morgan, Kristina S. Petersen, Penny M. Kris-Etherton, Trenton Wolfe, Dhimant Desai, Ethan H. Davis
article en

Abstract

Substituted indoles are conserved metabolites across all kingdoms of life and may function as a mediators of inter- and intra-species communication. Indole-3-carboxylates (indole-3-acetic acid (IAA) and indole-3-propionic acid (IPA)) represent abundant tryptophan-derived aryl hydrocarbon receptor (AHR) agonists in human serum, potentially influencing AHR-dependent physiology. LC-MS analysis of mouse serum, urine and cecal/fecal contents reveals that both IAA and IPA undergo host and microbial mediated glycine conjugation to facilitate urinary elimination. Notably, at physiologically detectable human serum concentrations (μM), IAA-Glycine retains human AHR activation potential. Comparative in silico docking simulations corroborate IAA-Glycine as a direct ligand for the human AHR. In contrast to xenobiotic ligands such as TCDD and FICZ, the endogenous tryptophan metabolites examined here exhibited greater activation associated with human AHR relative to mouse AHR. These results underscore the role of microbial and host-derived amino acid conjugation in generating bioactive metabolites and position auxin chemistry within human physiology. Glycine conjugates of indole-3-acetic acid and indole-3-propionic acid made by the host and/or the microbiome are Ah receptor agonists.

Communications Biology
Pennsylvania State University (US), Oregon State University (US), Montana State University (US), Penn State Milton S. Hershey Medical Center (US)
U.S. Department of Agriculture, National Institute of Environmental Research, National Institutes of Health, Huck Institutes of the Life Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, National Institute of Environmental Health Sciences
Openalex Percentile: Top 12%
Toxic Organic Pollutants Impact
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