Evidence map›Paper›PMID 32719140›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2020

Microbial tryptophan metabolites regulate gut barrier function via the aryl hydrocarbon receptor.

Samantha A Scott, Jingjing Fu, Pamela V Chang

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 392 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
392citing papers in PubMed, 1 pooled it
22.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

392 citing papers in PubMed, 1 synthesis or guideline pooled it, 570 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Bridging the gap:Gut microbes · 2026
    Review
  7. Article
  8. Indole-3-carboxaldehyde fromGut microbes · 2026
    Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. Article
  14. Review
  15. Anti-inflammatory activity of Chlorella polysaccharide AHP.Molecular and cellular biochemistry · 2026
    Article
  16. mSphere · 2026
    Article
  17. Review
  18. Article
  19. Article
  20. Review

332 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Samantha A ScottDepartment of Microbiology, Cornell University, Ithaca, NY 14853.ORCID 0000-0002-3752-9368
Jingjing FuDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY 14853.ORCID 0000-0001-6502-321X
Pamela V ChangDepartment of Microbiology and Immunology, Cornell University, Ithaca, NY 14853; pamela.chang@cornell.edu.ORCID 0000-0003-3819-9994
Cornell University · US

Funding

Activity-based protein profiling of gut microbiota-associated bile acid metabolismR35GM133501 · NIGMS · CORNELL UNIVERSITY · PI Pamela Vivian Chang · 2019 to 2026
$2.8M
NIGMS NIH HHS R35 GM133501
6 · The paper itself

Abstract

Inflammatory bowel diseases (IBDs), including Crohn's disease and ulcerative colitis, are associated with dysbiosis of the gut microbiome. Emerging evidence suggests that small-molecule metabolites derived from bacterial breakdown of a variety of dietary nutrients confer a wide array of host benefits, including amelioration of inflammation in IBDs. Yet, in many cases, the molecular pathways targeted by these molecules remain unknown. Here, we describe roles for three metabolites-indole-3-ethanol, indole-3-pyruvate, and indole-3-aldehyde-which are derived from gut bacterial metabolism of the essential amino acid tryptophan, in regulating intestinal barrier function. We determined that these metabolites protect against increased gut permeability associated with a mouse model of colitis by maintaining the integrity of the apical junctional complex and its associated actin regulatory proteins, including myosin IIA and ezrin, and that these effects are dependent on the aryl hydrocarbon receptor. Our studies provide a deeper understanding of how gut microbial metabolites affect host defense mechanisms and identify candidate pathways for prophylactic and therapeutic treatments for IBDs.

Indexed as

AnimalsBasic Helix-Loop-Helix ProteinsCaco-2 CellsColitis, UlcerativeCytoskeletal ProteinsDisease Models, AnimalEzrinGastrointestinal MicrobiomeHumansInflammationIntestinal MucosaMiceMice, KnockoutNonmuscle Myosin Type IIAPermeabilityReceptors, Aryl HydrocarbonAhr protein, mouseBasic Helix-Loop-Helix ProteinsCytoskeletal ProteinsEzrinNonmuscle Myosin Type IIAReceptors, Aryl HydrocarbonTryptophancolitisgut microbiomeinflammatory bowel diseaseintestinal epithelium

Identifiers

PMID32719140
PMCPMC7431026
OpenAlexW3045898304

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.