Evidence map›Paper›PMID 24124129›Full record

ArticleObesity (Silver Spring, Md.)2014

CXCR3 modulates obesity-induced visceral adipose inflammation and systemic insulin resistance.

Jeffrey A Deiuliis, Steve Oghumu, Dheeraj Duggineni, Jixin Zhong, Jessica Rutsky, Ambar Banerjee, Bradley Needleman, Dean Mikami, Vimal Narula, Jeffrey Hazey and 2 more

Open access · greenAbstract read
In one paragraph

Article in Obesity (Silver Spring, Md.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 49 citations in OpenAlex.

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  17. High Fat Diet-Induced CD8Frontiers in immunology · 2021
    Article
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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

12 authors at 2 institutions in 1 country.

Jeffrey A DeiuliisDavis Heart & Lung Research Institute, The Ohio State University College of Medicine, Columbus, Ohio, USA.
Steve Oghumu
Dheeraj Duggineni
Jixin Zhong
Jessica Rutsky
Ambar Banerjee
Bradley Needleman
Dean Mikami
Vimal Narula
Jeffrey Hazey
Abhay R Satoskar
Sanjay Rajagopalan
The Ohio State University · USLung Institute · US

Funding

Comprehensive Training in Oral &Craniofacial SciencesT32DE014320 · NIDCR · OHIO STATE UNIVERSITY · PI SHERIDAN, JOHN F · 2001 to 2022
$10.2M
Diet-Environment Interactions in InflammationR01ES017290 · NIEHS · UNIVERSITY OF MARYLAND BALTIMORE · PI RAJAGOPALAN, SANJAY · 2010 to 2014
$1.8M
The Ohio State University Center for Clinical and Translational Science (KL2)KL2TR000112 · NCATS · OHIO STATE UNIVERSITY · PI JACKSON, REBECCA D · 2012 to 2013
$855k
T Regulatory Cells as Determinants of Inflammation in Adipose TissueR21DK088522 · NIDDK · OHIO STATE UNIVERSITY · PI RAJAGOPALAN, SANJAY · 2010 to 2011
$417k
Inflammatory Mechanisms In Insulin ResistanceF32DK083903 · NIDDK · OHIO STATE UNIVERSITY · PI DEIULIIS, JEFFREY ALAN · 2009 to 2011
$157k
NCATS NIH HHS 8KL2TR000112-05NCATS NIH HHS KL2 TR000112NIDCR NIH HHS T32 DE014320NIDDK NIH HHS F32 DK083903NIDDK NIH HHS F32-DK083903NIDDK NIH HHS R21 DK088522NIDDK NIH HHS R21-DK088522NIEHS NIH HHS R0-1-ES017290NIEHS NIH HHS R01 ES017290
6 · The paper itself

Abstract

objectiveChemokine (C-X-C motif) receptor 3 (CXCR3) is a chemokine receptor involved in the regulation of immune cell trafficking and activation. Increased CXCR3 expression in the visceral adipose of obese humans and mice was observed. A pathophysiologic role for CXCR3 in diet-induced obesity (DIO) was hypothesized.

methodsWild-type (WT) C57B/L6J and chemokine receptor 3 knockout (CXCR3(-/-) ) mice were fed a high-fat diet (HFD) for 20 weeks followed by assessment of glucose metabolism and visceral adipose tissue (VAT) inflammation.

resultsCXCR3(-/-) mice exhibited lower fasting glucose and improved glucose tolerance compared with WT-HFD mice, despite similar body mass. HFD-induced VAT innate and adaptive immune cell infiltration, including immature myeloid cells (CD11b(+) F4/80(lo) Ly6C(+) ), were markedly ameliorated in CXCR3(-/-) mice. In vitro IBIDI and in vivo migration assays demonstrated no CXCR3-mediated effect on macrophage or monocyte migration, respectively. CXCR3(-/-) macrophages, however, had a blunted response to interferon-γ, a TH 1 cytokine that induces macrophage activation.

conclusionsA previously unreported role for CXCR3 in the development of HFD-induced insulin resistance (IR) and VAT macrophage infiltration in mice was demonstrated. Our results support pharmaceutical targeting of the CXCR3 receptor as a potential treatment for obesity/IR.

Indexed as

Insulin ResistanceAdultAnimalsBlood GlucoseBody Mass IndexCholesterol, HDLCholesterol, LDLDiet, High-FatGene TargetingHumansInflammationInsulinInterferon-gammaIntra-Abdominal FatMacrophage ActivationMacrophagesBlood GlucoseCholesterol, HDLCholesterol, LDLCXCR3 protein, humanCxcr3 protein, mouseInsulinInterferon-gammaReceptors, CXCR3Triglycerides

Identifiers

PMID24124129
PMCPMC4167757
OpenAlexW1604566598

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.