Evidence map›Paper›PMID 21980475›Full record

ArticlePloS one2011

Impact of CD1d deficiency on metabolism.

Maya E Kotas, Hui-Young Lee, Matthew P Gillum, Charles Annicelli, Blas A Guigni, Gerald I Shulman, Ruslan Medzhitov

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.2field-weighted citation impact, top 4% 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

52 citing papers in PubMed, 85 citations in OpenAlex.

  1. Review
  2. The PD-1/PD-L1 Axis in the Biology of MASLD.International journal of molecular sciences · 2024
    Review
  3. Review
  4. Effects of NKT Cells on Metabolic Disorders Caused by High-Fat Diet Using CD1d-Knockout Mice.Diabetes, metabolic syndrome and obesity : targets and therapy · 2023
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Review
  18. CD1d-Restricted pathways in hepatocytes control local natural killer T cell homeostasis and hepatic inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  19. Review
  20. 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

7 authors at 3 institutions in 1 country.

Maya E KotasDepartment of Immunobiology, Yale University School of Medicine, New Haven, Connecticut, United States of America. maya.kotas@gmail.com
Hui-Young Lee
Matthew P Gillum
Charles Annicelli
Blas A Guigni
Gerald I Shulman
Ruslan Medzhitov
Yale University · USHoward Hughes Medical Institute · USUniversity of Iowa · US

Funding

Yale Diabetes Research CenterP30DK045735 · NIDDK · YALE UNIVERSITY · PI Richard A Flavell · 1993 to 2026
$44.0M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007205 · NIGMS · YALE UNIVERSITY · PI KAZMIERCZAK, BARBARA I · 1985 to 2019
$42.9M
Yale Mouse Metabolic Phenotyping CenterU24DK059635 · NIDDK · YALE UNIVERSITY · PI SHULMAN, GERALD I · 2001 to 2015
$8.9M
Mechanisms of Lipid-Induced Hepatic Insulin ResistanceR01DK040936 · NIDDK · YALE UNIVERSITY · PI SHULMAN, GERALD I · 1989 to 2015
$5.1M
Cell Biology of TLR Signal TransductionR37AI046688 · NIAID · YALE UNIVERSITY · PI MEDZHITOV, RUSLAN · 2006 to 2015
$3.8M
Toll Pathway & Control of Adaptive Immune ResponsesR01AI055502 · NIAID · YALE UNIVERSITY · PI MEDZHITOV, RUSLAN · 2003 to 2013
$3.7M
Role of basophils in initiating Th2 immune responsesR01AI089771 · NIAID · YALE UNIVERSITY · PI MEDZHITOV, RUSLAN · 2010 to 2014
$2.0M
TOLL RECEPTORS AND CONTROL OF MAMMALIAN IMMUNITYR01AI046688 · NIAID · YALE UNIVERSITY · PI MEDZHITOV, RUSLAN · 2001 to 2005
$1.5M
Howard Hughes Medical InstituteNIAID NIH HHS AI046688NIAID NIH HHS AI055502NIAID NIH HHS AI089771NIAID NIH HHS R01 AI046688NIAID NIH HHS R01 AI055502NIAID NIH HHS R01 AI089771NIAID NIH HHS R37 AI046688NIDDK NIH HHS DK 045735NIDDK NIH HHS DK R01 40936NIDDK NIH HHS P30 DK045735NIDDK NIH HHS R01 DK040936NIDDK NIH HHS U24 DK 059635NIDDK NIH HHS U24 DK059635NIGMS NIH HHS T32 GM007205NIGMS NIH HHS TG 2T32GM07205
6 · The paper itself

Abstract

Invariant natural killer T cells (iNKTs) are innate-like T cells that are highly concentrated in the liver and recognize lipids presented on the MHC-like molecule CD1d. Although capable of a myriad of responses, few essential functions have been described for iNKTs. Among the many cell types of the immune system implicated in metabolic control and disease, iNKTs seem ideally poised for such a role, yet little has been done to elucidate such a possible function. We hypothesized that lipid presentation by CD1d could report on metabolic status and engage iNKTs to regulate cellular lipid content through their various effector mechanisms. To test this hypothesis, we examined CD1d deficient mice in a variety of metabolically stressed paradigms including high fat feeding, choline-deficient feeding, fasting, and acute inflammation. CD1d deficiency led to a mild exacerbation of steatosis during high fat or choline-deficient feeding, accompanied by impaired hepatic glucose tolerance. Surprisingly, however, this phenotype was not observed in Jα18⁻/⁻ mice, which are deficient in iNKTs but express CD1d. Thus, CD1d appears to modulate some metabolic functions through an iNKT-independent mechanism.

Indexed as

AnimalsAntigens, CD1dBody WeightChemokine CXCL16Chemokine CXCL6CholineDiet, High-FatFatty LiverGene Expression RegulationGlucose IntoleranceHumansInsulinLiverMaleMiceNatural Killer T-CellsAntigens, CD1dChemokine CXCL16Chemokine CXCL6CholineCxcl16 protein, mouseInsulin

Identifiers

PMID21980475
PMCPMC3183002
OpenAlexW2012582093

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.