Evidence map›Paper›PMID 34214492›Full record

ArticleCell host & microbe2021

Commensal microbiota regulates skin barrier function and repair via signaling through the aryl hydrocarbon receptor.

Aayushi Uberoi, Casey Bartow-McKenney, Qi Zheng, Laurice Flowers, Amy Campbell, Simon A B Knight, Neal Chan, Monica Wei, Victoria Lovins, Julia Bugayev and 9 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 187 papers.

0numbers the graph read from it
0cells of the map it votes in
187citing papers in PubMed
36.2field-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

187 citing papers in PubMed, 280 citations in OpenAlex.

  1. Trial
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  9. Epithelial-Dermal Immune Memory: TrackingInternational journal of molecular sciences · 2026
    Review
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  19. The dual role of the microbiome in chronic wound management.Cell communication and signaling : CCS · 2026
    Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 4 institutions in 1 country.

Aayushi UberoiDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Casey Bartow-McKenneyDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Qi ZhengDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Laurice FlowersDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Amy CampbellDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Simon A B KnightDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Neal ChanDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Monica WeiDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Victoria LovinsDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Julia BugayevDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Joseph HorwinskiDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA.
Charles BradleyDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, PA, USA.
Jason MeyerSan Francisco Veterans Affairs Medical Center, Dermatology Service, San Francisco, CA, USA; Department of Dermatology, University of California San Francisco, San Francisco, CA, USA.
Debra CrumrineSan Francisco Veterans Affairs Medical Center, Dermatology Service, San Francisco, CA, USA; Department of Dermatology, University of California San Francisco, San Francisco, CA, USA.
Carrie Hayes SutterDepartment of Biological Sciences, W. Harry Feinstone Center for Genomic Research, University of Memphis, Memphis, TN, USA.
Peter EliasSan Francisco Veterans Affairs Medical Center, Dermatology Service, San Francisco, CA, USA; Department of Dermatology, University of California San Francisco, San Francisco, CA, USA.
Elizabeth MauldinDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, PA, USA.
Thomas R SutterDepartment of Biological Sciences, W. Harry Feinstone Center for Genomic Research, University of Memphis, Memphis, TN, USA. Electronic address: tsutter@memphis.edu.
Elizabeth A GriceDepartment of Dermatology, Perelman School of Medicine, University of Pennsylvania, PA, USA. Electronic address: egrice@pennmedicine.upenn.edu.
University of Pennsylvania · USUniversity of California, San Francisco · USUniversity of Memphis · USSan Francisco VA Medical Center · US

Funding

Penn Dermatology Research Training ProgramT32AR007465 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Elizabeth Anne Grice, David Joel Margolis · 1986 to 2026
$9.0M
Study Design and Data AnalysisP30AR069589 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI Elizabeth Anne Grice · 2016 to 2026
$8.6M
Cellular Determinants of AH Receptor SignalingR01ES017014 · NIEHS · UNIVERSITY OF MEMPHIS · PI THOMAS R SUTTER · 2010 to 2026
$4.3M
Decoding the microbial burden in diabetic foot ulcersR01NR015639 · NINR · UNIVERSITY OF PENNSYLVANIA · PI GRICE, ELIZABETH ANNE · 2015 to 2023
$4.1M
The Microbiome of Impaired Wound HealingR00AR060873 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI GRICE, ELIZABETH ANNE · 2012 to 2014
$730k
Skin microbiome interactions with neonatal aryl hydrocarbon receptor signaling: roles in cutaneous barrier function, inflammation, and toleranceR56ES030218 · NIEHS · UNIVERSITY OF PENNSYLVANIA · PI GRICE, ELIZABETH ANNE, SUTTER, THOMAS R · 2019 to 2019
$161k
NIAMS NIH HHS P30 AR069589NIAMS NIH HHS R00 AR060873NIAMS NIH HHS T32 AR007465NIEHS NIH HHS R01 ES017014NIEHS NIH HHS R56 ES030218NINR NIH HHS R01 NR015639
6 · The paper itself

Abstract

The epidermis forms a barrier that defends the body from desiccation and entry of harmful substances, while also sensing and integrating environmental signals. The tightly orchestrated cellular changes needed for the formation and maintenance of this epidermal barrier occur in the context of the skin microbiome. Using germ-free mice, we demonstrate the microbiota is necessary for proper differentiation and repair of the epidermal barrier. These effects are mediated by microbiota signaling through the aryl hydrocarbon receptor (AHR) in keratinocytes, a xenobiotic receptor also implicated in epidermal differentiation. Mice lacking keratinocyte AHR are more susceptible to barrier damage and infection, during steady-state and epicutaneous sensitization. Colonization with a defined consortium of human skin isolates restored barrier competence in an AHR-dependent manner. We reveal a fundamental mechanism whereby the microbiota regulates skin barrier formation and repair, which has far-reaching implications for the numerous skin disorders characterized by epidermal barrier dysfunction.

Indexed as

Signal TransductionAnimalsBasic Helix-Loop-Helix ProteinsCell DifferentiationCell LineEpidermal CellsEpidermisFemaleHumansKeratinocytesMaleMiceMice, Inbred C57BLMicrobiotaReceptors, Aryl HydrocarbonSkinAHR protein, humanBasic Helix-Loop-Helix ProteinsReceptors, Aryl Hydrocarbonaryl hydrocarbon receptorepidermiskeratinocytemicrobiotaskin barrierskin commensalsskin microbiome

Identifiers

PMID34214492
PMCPMC8364505
OpenAlexW3176332101

What OpenQuestion holds

Textmetadata
LicenceTDM
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.