Evidence map›Paper›PMID 24386254›Full record

ArticlePloS one2013

Inflammatory cytokine gene expression in mesenteric adipose tissue during acute experimental colitis.

W Conan Mustain, Marlene E Starr, Joseph D Valentino, Donald A Cohen, Daiki Okamura, Chi Wang, B Mark Evers, Hiroshi Saito

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Creeping fat and gut microbiota in Crohn's disease.World journal of gastroenterology · 2025
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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

8 authors at 2 institutions in 1 country.

W Conan MustainMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America ; Department of Surgery, University of Kentucky, Lexington, Kentucky, United States of America.
Marlene E StarrMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America ; Department of Surgery, University of Kentucky, Lexington, Kentucky, United States of America.
Joseph D ValentinoMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America ; Department of Surgery, University of Kentucky, Lexington, Kentucky, United States of America.
Donald A CohenDepartment of Microbiology, Immunology, and Molecular Genetics, University of Kentucky, Lexington, Kentucky, United States of America.
Daiki OkamuraMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America ; Department of Surgery, University of Kentucky, Lexington, Kentucky, United States of America.
Chi WangMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America ; Department of Biostatistics, University of Kentucky, Lexington, Kentucky, United States of America.
B Mark EversMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America ; Department of Surgery, University of Kentucky, Lexington, Kentucky, United States of America.
Hiroshi SaitoMarkey Cancer Center, University of Kentucky, Lexington, Kentucky, United States of America ; Department of Surgery, University of Kentucky, Lexington, Kentucky, United States of America ; Department of Physiology, University of Kentucky, Lexington, Kentucky, United States of America.
Markey Cancer Center · USUniversity of Kentucky · US

Funding

SURGICAL STUDIES OF FUNCTIONAL GENE EXPRESSIONR01DK048498 · NIDDK · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI EVERS, BERNARD MARK · 1996 to 2023
$7.9M
The Role of Adipose Tissue in Age-dependent Sensitivity to Critical IllnessR01AG039732 · NIA · UNIVERSITY OF KENTUCKY · PI SAITO, HIROSHI · 2011 to 2015
$1.5M
NIA NIH HHS R01 AG039732NIDDK NIH HHS R01 DK048498
6 · The paper itself

Abstract

backgroundProduction of inflammatory cytokines by mesenteric adipose tissue (MAT) has been implicated in the pathogenesis of inflammatory bowel disease (IBD). Animal models of colitis have demonstrated inflammatory changes within MAT, but it is unclear if these changes occur in isolation or as part of a systemic adipose tissue response. It is also unknown what cell types are responsible for cytokine production within MAT. The present study was designed to determine whether cytokine production by MAT during experimental colitis is depot-specific, and also to identify the source of cytokine production within MAT.

methodsExperimental colitis was induced in 6-month-old C57BL/6 mice by administration of dextran sulfate sodium (2% in drinking water) for up to 5 days. The induction of cytokine mRNA within various adipose tissues, including mesenteric, epididymal, and subcutaneous, was analyzed by qRT-PCR. These adipose tissues were also examined for histological evidence of inflammation. The level of cytokine mRNA during acute colitis was compared between mature mesenteric adipocytes, mesenteric stromal vascular fraction (SVF), and mesenteric lymph nodes.

resultsDuring acute colitis, MAT exhibited an increased presence of infiltrating mononuclear cells and fibrotic structures, as well as decreased adipocyte size. The mRNA levels of TNF-α, IL-1β, and IL-6 were significantly increased in MAT but not other adipose tissue depots. Within the MAT, induction of these cytokines was observed mainly in the SVF.

conclusionsAcute experimental colitis causes a strong site-specific inflammatory response within MAT, which is mediated by cells of the SVF, rather than mature adipocytes or mesenteric lymph nodes.

Indexed as

Gene ExpressionAcute DiseaseAdipose TissueAnimalsColitisCytokinesDextran SulfateDisease Models, AnimalDisease ProgressionInflammationInflammation MediatorsMaleMesenteryMiceTime FactorsCytokinesDextran SulfateInflammation Mediators

Identifiers

PMID24386254
PMCPMC3873328
OpenAlexW2023012759

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.