Evidence map›Paper›PMID 23922382›Full record

ArticleJournal of lipid research2013

Increased levels of invariant natural killer T lymphocytes worsen metabolic abnormalities and atherosclerosis in obese mice.

Savitha Subramanian, Michael S Turner, Yilei Ding, Leela Goodspeed, Shari Wang, Jane H Buckner, Kevin O'Brien, Godfrey S Getz, Catherine A Reardon, Alan Chait

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-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

18 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Article
  5. T Cells in Adipose Tissue in Aging.Frontiers in immunology · 2018
    Review
  6. Review
  7. Review
  8. Natural killer T cells in atherosclerosis.Nature reviews. Cardiology · 2017
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. 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

10 authors at 3 institutions in 1 country.

Savitha SubramanianDivision of Metabolism, Endocrinology and Nutrition and University of Washington, Seattle, WA.
Michael S Turner
Yilei Ding
Leela Goodspeed
Shari Wang
Jane H Buckner
Kevin O'Brien
Godfrey S Getz
Catherine A Reardon
Alan Chait
University of Washington · USUniversity of Chicago · USBenaroya Research Institute

Funding

Vector and Transgenic Mouse CoreP30DK017047 · NIDDK · UNIVERSITY OF WASHINGTON · PI Sakeneh Zraika · 1986 to 2026
$41.4M
PILOT STUDY--CLINICAL NUTRITION RESEARCHP30DK035816 · NIDDK · UNIVERSITY OF WASHINGTON · PI Ellen A Schur · 1986 to 2026
$30.4M
Role of Serum Amyloid A in Diabetic Vascular DiseaseP01HL092969 · NHLBI · UNIVERSITY OF WASHINGTON · PI VAISAR, TOMAS · 2008 to 2019
$23.5M
Nutrition, Obesity and Atherosclerosis Training ProgramT32HL007028 · NHLBI · UNIVERSITY OF WASHINGTON · PI Karin E Bornfeldt · 1985 to 2026
$6.4M
NKT cells in lipoprotein Metabolism and atherosclerosisR01HL088420 · NHLBI · UNIVERSITY OF CHICAGO · PI GETZ, GODFREY SHALOM · 2008 to 2011
$1.5M
FREE FATTY ACID INHIBITORS IN GLOBAL MYOCARDIAL ISCHEMIAF32HL009352 · NHLBI · DUKE UNIVERSITY · PI HENDRICKSON, STEVEN C · 1995 to 1995
–
NHLBI NIH HHS F32 HL009352NHLBI NIH HHS HL-092969NHLBI NIH HHS HL-09352NHLBI NIH HHS HL-88420NHLBI NIH HHS P01 HL092969NHLBI NIH HHS R01 HL088420NHLBI NIH HHS T32 HL007028NIDDK NIH HHS DK-035816NIDDK NIH HHS P30 DK017047NIDDK NIH HHS P30 DK035816
6 · The paper itself

Abstract

Obesity is a chronic inflammatory state characterized by infiltration of adipose tissue by immune cell populations, including T lymphocytes. Natural killer T (NKT) cells, a specialized lymphocyte subset recognizing lipid antigens, can be pro- or anti-inflammatory. Their role in adipose inflammation continues to be inconclusive and contradictory. In obesity, the infiltration of tissues by invariant NKT (iNKT) cells is decreased. We therefore hypothesized that an excess iNKT cell complement might improve metabolic abnormalities in obesity. Vα14 transgenic (Vα14tg) mice, with increased iNKT cell numbers, on a LDL receptor-deficient (Ldlr(-/-)) background and control Ldlr(-/-) mice were placed on an obesogenic diet for 16 weeks. Vα14tg.Ldlr(-/-) mice gained 25% more weight and had increased adiposity than littermate controls. Transgenic mice also developed greater dyslipidemia, hyperinsulinemia, insulin resistance, and hepatic triglyceride accumulation. Increased macrophage Mac2 immunostaining and proinflammatory macrophage gene expression suggested worsened adipose inflammation. Concurrently, these mice had increased atherosclerotic lesion area and aortic inflammation. Thus, increasing the complement of iNKT cells surprisingly exacerbated the metabolic, inflammatory, and atherosclerotic features of obesity. These findings suggest that the reduction of iNKT cells normally observed in obesity may represent a physiological attempt to compensate for this inflammatory condition.

Indexed as

Adipose Tissue, WhiteAdiposityAnimalsAortaAtherosclerosisCD4 Lymphocyte CountDiet, High-FatFatty LiverHypercholesterolemiaHypertriglyceridemiaMacrophagesMaleMiceMice, Inbred C57BLMice, KnockoutMice, ObeseSucroseadipose tissueantigensinflammationlipidssteatosis

Identifiers

PMID23922382
PMCPMC3770095
OpenAlexW2127998208

What OpenQuestion holds

Textmetadata
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.