Evidence map›Paper›PMID 36214220›Full record

ArticleJCI insight2022

CD11c+ myeloid cell exosomes reduce intestinal inflammation during colitis.

Kaylyn M Bauer, Morgan C Nelson, William W Tang, Tyson R Chiaro, D Garrett Brown, Arevik Ghazaryan, Soh-Hyun Lee, Allison M Weis, Jennifer H Hill, Kendra A Klag and 12 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 19 citations in OpenAlex.

  1. Rab27: Molecular switch of tumor exosome secretion (Review).International journal of molecular medicine · 2026
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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

22 authors at 1 institution in 1 country.

Kaylyn M BauerDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Morgan C NelsonDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
William W TangDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Tyson R ChiaroDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
D Garrett BrownDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Arevik GhazaryanDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Soh-Hyun LeeDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Allison M WeisDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Jennifer H HillDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Kendra A KlagDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Van B TranDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Jacob W ThompsonDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Andrew G RamsteadDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Josh K MontsUniversity of Utah Flow Cytometry Core, Salt Lake City, Utah, USA.
James E MarvinUniversity of Utah Flow Cytometry Core, Salt Lake City, Utah, USA.
Margaret AlexanderDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Warren P VothDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
W Zac StephensDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Diane M WardDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Aaron C PetreyDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
June L RoundDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
Ryan M O'ConnellDepartment of Pathology, Division of Microbiology and Immunology, University of Utah, Salt Lake City, Utah, USA.
University of Utah · US

Funding

Interdisciplinary Training Program in MetabolismT32DK091317 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI SCOTT A SUMMERS · 2011 to 2026
$4.8M
Training Program in Genomic MedicineT32HG008962 · NHGRI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Lynn Jorde, Aaron R Quinlan · 2016 to 2026
$3.0M
Investigating the transfer of miRNAs by exosomes during inflammationR01AI123106 · NIAID · UNIVERSITY OF UTAH · PI O'CONNELL, RYAN M · 2017 to 2021
$2.0M
Cross-disciplinary Training in Immunology, Inflammation and Infectious DiseaseT32AI138945 · NIAID · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Tracey Jane Lamb, Matthew A Williams · 2018 to 2026
$1.6M
T cell expressed miR-155 promotes antitumor immunity and immune checkpoint blockade responses in colon cancer through repression of Ship1F30CA260977 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI TANG, WILLIAM WEIHAO · 2021 to 2025
$252k
Investigating Metabolically Protective Members of the Microbiota that Modulate CeramidesF30DK127846 · NIDDK · UNIVERSITY OF UTAH · PI KLAG, KENDRA ALYSE · 2021 to 2024
$197k
NIAID NIH HHS R01 AI123106NIAID NIH HHS T32 AI138945
6 · The paper itself

Abstract

Intercellular communication is critical for homeostasis in mammalian systems, including the gastrointestinal (GI) tract. Exosomes are nanoscale lipid extracellular vesicles that mediate communication between many cell types. Notably, the roles of immune cell exosomes in regulating GI homeostasis and inflammation are largely uncharacterized. By generating mouse strains deficient in cell-specific exosome production, we demonstrate deletion of the small GTPase Rab27A in CD11c+ cells exacerbated murine colitis, which was reversible through administration of DC-derived exosomes. Profiling RNAs within colon exosomes revealed a distinct subset of miRNAs carried by colon- and DC-derived exosomes. Among antiinflammatory exosomal miRNAs, miR-146a was transferred from gut immune cells to myeloid and T cells through a Rab27-dependent mechanism, targeting Traf6, IRAK-1, and NLRP3 in macrophages. Further, we have identified a potentially novel mode of exosome-mediated DC and macrophage crosstalk that is capable of skewing gut macrophages toward an antiinflammatory phenotype. Assessing clinical samples, RAB27A, select miRNAs, and RNA-binding proteins that load exosomal miRNAs were dysregulated in ulcerative colitis patient samples, consistent with our preclinical mouse model findings. Together, our work reveals an exosome-mediated regulatory mechanism underlying gut inflammation and paves the way for potential use of miRNA-containing exosomes as a novel therapeutic for inflammatory bowel disease.

Indexed as

CD11 AntigensColitisExosomesInflammationMyeloid CellsAnimalsInflammatory Bowel DiseasesIntestinesLipidsMammalsMiceMicroRNAsMonomeric GTP-Binding ProteinsNLR Family, Pyrin Domain-Containing 3 ProteinTNF Receptor-Associated Factor 6CD11 AntigensLipidsMicroRNAsMonomeric GTP-Binding ProteinsNLR Family, Pyrin Domain-Containing 3 ProteinTNF Receptor-Associated Factor 6Cell BiologyImmunologyInflammatory bowel diseaseNoncoding RNAs

Identifiers

PMID36214220
PMCPMC9675566
OpenAlexW4303926936

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.