Evidence map›Paper›PMID 24465369›Full record

ArticlePloS one2014

Mice lacking natural killer T cells are more susceptible to metabolic alterations following high fat diet feeding.

Brittany V Martin-Murphy, Qiang You, Hong Wang, Becky A De La Houssaye, Timothy P Reilly, Jacob E Friedman, Cynthia Ju

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 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

42 citing papers in PubMed, 60 citations in OpenAlex.

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  8. 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
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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

7 authors at 4 institutions in 2 countries.

Brittany V Martin-MurphyBarbara Davis Center for Diabetes, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Qiang YouDepartment of Biotherapy, Second Affiliated Hospital, Nanjing Medical University, Nanjing, Jiangsu, China ; Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Hong WangDivision of Endocrinology, Diabetes & Metabolism, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Becky A De La HoussayeDepartment of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Timothy P ReillyDrug Safety Evaluation, Research & Development, Bristol-Myers Squibb Company, Princeton, New Jersey, United States of America.
Jacob E FriedmanDepartment of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
Cynthia JuSkaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora, Colorado, United States of America.
University of Colorado Anschutz Medical Campus · USBristol-Myers Squibb (United States) · USSecond Affiliated Hospital of Nanjing Medical University · CNUniversity of Montana · US

Funding

PILOT STUDY--SUBSTRATE METABOLISM IN EXTREMELY LOW BIRTH WEIGHT INFANTSP30DK048520 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI Edward L Melanson · 1995 to 2026
$32.6M
Regulation of Glucose Homestasis by C/EBPBR01DK059767 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI FRIEDMAN, JACOB E · 2000 to 2010
$2.6M
The immunosuppressive role of hepatic Kupffer cellsR01ES012914 · NIEHS · UNIVERSITY OF COLORADO DENVER · PI JU, CYNTHIA · 2005 to 2009
$1.3M
Investigation of the role of DAMP molecules in the pathogenesis of Liver InjuryF31DK082269 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI MURPHY, BRITTANY V · 2008 to 2012
$127k
NIDDK NIH HHS F31 DK082269NIDDK NIH HHS F31DK082269NIDDK NIH HHS P30 DK048520NIDDK NIH HHS P30DK048520NIDDK NIH HHS R01 DK059767NIDDK NIH HHS R01-DK059767NIEHS NIH HHS R01 ES012914NIEHS NIH HHS R01ES012914
6 · The paper itself

Abstract

Current estimates suggest that over one-third of the adult population has metabolic syndrome and three-fourths of the obese population has non-alcoholic fatty liver disease (NAFLD). Inflammation in metabolic tissues has emerged as a universal feature of obesity and its co-morbidities, including NAFLD. Natural Killer T (NKT) cells are a subset of innate immune cells that abundantly reside within the liver and are readily activated by lipid antigens. There is general consensus that NKT cells are pivotal regulators of inflammation; however, disagreement exists as to whether NKT cells exert pathogenic or suppressive functions in obesity. Here we demonstrate that CD1d(-/-) mice, which lack NKT cells, were more susceptible to weight gain and fatty liver following high fat diet (HFD) feeding. Compared with their WT counterparts, CD1d(-/-) mice displayed increased adiposity and greater induction of inflammatory genes in the liver suggestive of the precursors of NAFLD. Calorimetry studies revealed a significant increase in food intake and trends toward decreased metabolic rate and activity in CD1d(-/-) mice compared with WT mice. Based on these findings, our results suggest that NKT cells play a regulatory role that helps to prevent diet-induced obesity and metabolic dysfunction and may play an important role in mechanisms governing cross-talk between metabolism and the immune system to regulate energy balance and liver health.

Indexed as

AnimalsAntigens, CD1dCalorimetry, IndirectDiet, High-FatFemaleImmunoblottingMiceMice, Inbred BALB CMice, KnockoutNatural Killer T-CellsObesityRNA, MessengerAntigens, CD1dRNA, Messenger

Identifiers

PMID24465369
PMCPMC3896335
OpenAlexW1966525151

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.