Evidence map›Paper›PMID 25856311›Full record

ArticlePloS one2015

Age-related onset of obesity corresponds with metabolic dysregulation and altered microglia morphology in mice deficient for Ifitm proteins.

Yin Shen Wee, Janis J Weis, Lorise C Gahring, Scott W Rogers, John H Weis

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Increased mRNA Levels ofBiomedicines · 2022
    Article
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  6. Article
  7. Article
  8. Review
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  13. Review
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  15. Article
  16. Hypothalamic inflammation and gliosis in obesity.Current opinion in endocrinology, diabetes, and obesity · 2015
    Review
  17. Article
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

5 authors at 1 institution in 1 country.

Yin Shen WeeDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.
Janis J WeisDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.
Lorise C GahringGeriatric Research, Education and Clinical Center (GRECC), Veterans Affairs Medical Center, Salt Lake City, Utah, United States of America; Department of Internal Medicine, Division of Geriatrics, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.
Scott W RogersGeriatric Research, Education and Clinical Center (GRECC), Veterans Affairs Medical Center, Salt Lake City, Utah, United States of America; Department of Neurobiology and Anatomy, Salt Lake City, Utah, United States of America.
John H WeisDepartment of Pathology, Division of Microbiology and Immunology, University of Utah School of Medicine, Salt Lake City, Utah, United States of America.
University of Utah · US

Funding

Mechanisms of TNFa Enhancement of Nicotinic Receptor UpregulationR01DA025057 · NIDA · UNIVERSITY OF UTAH · PI GAHRING, LORISE C, ROGERS, SCOTT WARREN · 2009 to 2013
$1.8M
Nicotinic Receptor Alpha 7 Regulation of Inflammation Induced by Cigarette SmokeI01BX001798 · VA · VA SALT LAKE CITY HEALTHCARE SYSTEM · PI GAHRING, LORISE C · 2015 to 2018
–
SITE SPECIFIC MUTAGENESIS OF H PYLORI CARBONIC ANHYDRASER15AI045521 · NIAID · COLGATE UNIVERSITY · PI ROWLETT, ROGER S · 1999 to 1999
–
BLRD VA I01 BX001798NIAID NIH HHS AI32773NIAID NIH HHS AI45521NIDA NIH HHS DA025057NIDA NIH HHS R01 DA025057
6 · The paper itself

Abstract

The IfitmDel mouse lacks all five of the Ifitm genes via LoxP deletion. This animal breeds normally with no obvious defect in development. The IfitmDel animals exhibit a steady and significantly enhanced weight gain relative to wild-type controls beginning about three months of age and under normal feeding conditions. The increased weight corresponds with elevated fat mass, and in tolerance tests they are hyporesponsive to insulin but respond normally to glucose. Both young (4 mo) and older (12 mo) IfitmDel mice have enhanced levels of serum leptin suggesting a defect in leptin/leptin receptor signaling. Analysis of the gene expression profiles in the hypothalamus of IfitmDel animals, compared to WT, demonstrated an altered ratio of Pomc and Npy neuropeptide expression, which likely impairs the satiation response of the IfitmDel animal leading to an increased eating behavior. Also elevated in hypothalamus of IfitmDel mice were pro-inflammatory cytokine expression and reduced IL-10. Anatomical analysis of the hypothalamus using immunohistochemistry revealed that microglia exhibit an abnormal morphology in IfitmDel animals and respond abnormally to Poly:IC challenge. These abnormalities extend the phenotype of the IfitmDel mouse beyond abnormal responses to viral challenge to include a metabolic phenotype and weight gain. Further, this novel phenotype for the IfitmDel mouse could be related to abnormal neuropeptide production, inflammatory status and microglia status in the hypothalamus.

Indexed as

Age of OnsetAnimalsAntigens, DifferentiationCytokinesGene DeletionGene Expression ProfilingHypothalamusImmunohistochemistryLeptinMetabolic Networks and PathwaysMiceMicrogliaMultigene FamilyNeuropeptide YObesityPro-OpiomelanocortinAntigens, DifferentiationCytokinesLeptinleu-13 antigenNeuropeptide YPro-Opiomelanocortin

Identifiers

PMID25856311
PMCPMC4391874
OpenAlexW2075533061

What OpenQuestion holds

Textmetadata
LicenceCC0
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.