Evidence map›Paper›PMID 25333972›Full record

ArticlePloS one2014

Role of NKG2D in obesity-induced adipose tissue inflammation and insulin resistance.

Jun-Jae Chung, Mary A Markiewicz, Bojan Polić, Andrey S Shaw

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 16 citations in OpenAlex.

  1. Review
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  9. Innate Lymphoid Cell Immunometabolism.Journal of molecular biology · 2017
    Review
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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

4 authors at 2 institutions in 2 countries.

Jun-Jae ChungDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Mary A MarkiewiczDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Bojan PolićDepartment of Histology and Embryology, University of Rijeka School of Medicine, Rijeka, Croatia.
Andrey S ShawDepartment of Pathology and Immunology, Washington University School of Medicine, St. Louis, Missouri, United States of America; Howard Hughes Medical Institute, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Washington University in St. Louis · USUniversity of Rijeka · HR

Funding

WU P&FP30DK020579 · NIDDK · WASHINGTON UNIVERSITY · PI Jennifer Lynn Powers Carson · 2013 to 2026
$27.1M
STRUCTURE AND FUNCTION OF CD2AP IN THE KIDNEYR01DK058366 · NIDDK · WASHINGTON UNIVERSITY · PI MINER, JEFFREY H · 2000 to 2019
$6.8M
Howard Hughes Medical InstituteNIDDK NIH HHS P30 DK020579NIDDK NIH HHS R01 DK058366NIDDK NIH HHS R01DK058366
6 · The paper itself

Abstract

The early events that initiate inflammation in the adipose tissue during obesity are not well defined. It is unclear whether the recruitment of CD8 T cells to the adipose tissue during onset of obesity occurs through antigen-dependent or -independent processes. We have previously shown that interaction between NKG2D (natural-killer group 2, member D) and its ligand Rae-1ε is sufficient to recruit cytotoxic T lymphocytes to the pancreas and induce insulitis. Here, we tested whether NKG2D-NKG2D ligand interaction is also involved in obesity-induced adipose tissue inflammation and insulin resistance. We observed a significant induction of NKG2D ligand expression in the adipose tissue of obese mice, especially during the early stages of obesity. However, mice lacking NKG2D developed similar levels of insulin resistance and adipose tissue inflammation compared to control mice when placed on a high-fat diet. Moreover, overexpression of Rae-1ε in the adipose tissue did not increase immune cell infiltration to the adipose tissue either in the setting of a normal or high-fat diet. These results indicate that, unlike in the pancreas, NKG2D-NKG2D ligand interaction does not play a critical role in obesity-induced inflammation in the adipose tissue.

Indexed as

3T3-L1 CellsAdipocytesAdipose TissueAnimalsDisease Models, AnimalGene ExpressionInsulinInsulin ResistanceLigandsMaleMiceMice, KnockoutNK Cell Lectin-Like Receptor Subfamily KNuclear Matrix-Associated ProteinsNucleocytoplasmic Transport ProteinsObesityInsulinKlrk1 protein, mouseLigandsNK Cell Lectin-Like Receptor Subfamily KNuclear Matrix-Associated ProteinsNucleocytoplasmic Transport ProteinsRae1 protein, mouseTumor Necrosis Factor-alpha

Identifiers

PMID25333972
PMCPMC4198197
OpenAlexW1988573710

What OpenQuestion holds

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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.