Evidence map›Paper›PMID 29035781›Full record

ArticleAtherosclerosis2017

Lack of myeloid Fatp1 increases atherosclerotic lesion size in Ldlr

Liyang Zhao, Alyssa J Cozzo, Amy R Johnson, Taylor Christensen, Alex J Freemerman, James E Bear, Jeremy D Rotty, Brian J Bennett, Liza Makowski

Open access · greenAbstract read
In one paragraph

Article in Atherosclerosis, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Metabolite transporters as regulators of macrophage polarization.Naunyn-Schmiedeberg's archives of pharmacology · 2022
    Review
  4. Article
  5. Review
  6. Review
  7. Friend or Foe? Recent Strategies to Target Myeloid Cells in Cancer.Frontiers in cell and developmental biology · 2020
    Review
  8. MyeloidJournal of immunology (Baltimore, Md. : 1950) · 2019
    Article
  9. Article
  10. Review
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

9 authors at 3 institutions in 1 country.

Liyang ZhaoDepartment of Nutrition, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA.
Alyssa J CozzoDepartment of Nutrition, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA.
Amy R JohnsonDepartment of Nutrition, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA.
Taylor ChristensenDepartment of Nutrition, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA.
Alex J FreemermanDepartment of Nutrition, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA.
James E BearLineberger Cancer Center, Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, USA.
Jeremy D RottyLineberger Cancer Center, Department of Cell Biology and Physiology, University of North Carolina, Chapel Hill, NC 27599, USA.
Brian J BennettUSDA Western Human Nutrition Research Center, Davis, CA 95616, USA.
Liza MakowskiDepartment of Nutrition, Gillings School of Global Public Health, University of North Carolina, Chapel Hill, NC 27599, USA; Department of Medicine, University of North Carolina, Chapel Hill, NC 27599, USA; University of Tennessee Health Science Center, Memphis, TN 38163, USA. Electronic address: Liza.makowski@uthsc.edu.
University of North Carolina at Chapel Hill · USUNC Lineberger Comprehensive Cancer CenterWestern Human Nutrition Research Center · US

Funding

UNIV OF NORTH CAROLINA CLINICAL NUTRITION RESEARCH UNITP30DK056350 · NIDDK · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Ian Michael Carroll · 1999 to 2026
$31.6M
Pre-doctoral Training Program in Integrative Vascular BiologyT32HL069768 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Christopher P. Mack · 2002 to 2026
$9.7M
Systems Genetic Studies of TMAO regulation and AtherosclerosisR01HL128572 · NHLBI · U.S. AGRICULTURAL RESEARCH SERVICE · PI BENNETT, BRIAN JOSEPH · 2015 to 2019
$1.4M
The Coordination of Cytoskeletal Dynamics by CoroninsR01GM083035 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BEAR, JAMES E · 2007 to 2011
$1.2M
Macrophage Mitochondrial Stress in Inflammation, Insulin Resistance & ObesityR00AA017376 · NIAAA · UNIV OF NORTH CAROLINA CHAPEL HILL · PI MAKOWSKI-HAYES, LIZA · 2010 to 2012
$728k
The Role of Substrate Metabolism and Macrophage Activation in ObesityF32HL117616 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI JOHNSON, AMY · 2013 to 2015
$107k
NHLBI NIH HHS F32 HL117616NHLBI NIH HHS R01 HL128572NHLBI NIH HHS T32 HL069768NIAAA NIH HHS R00 AA017376NIDDK NIH HHS P30 DK056350NIGMS NIH HHS R01 GM083035
6 · The paper itself

Abstract

BACKGROUND AND

aimsAltered metabolism is an important regulator of macrophage (MΦ) phenotype, which contributes to inflammatory diseases such as atherosclerosis. Broadly, pro-inflammatory, classically-activated MΦs (CAM) are glycolytic while alternatively-activated MΦs (AAM) oxidize fatty acids, although overlap exists. We previously demonstrated that MΦ fatty acid transport protein 1 (FATP1, Slc27a1) was necessary to maintain the oxidative and anti-inflammatory AAM phenotype in vivo in a model of diet-induced obesity. The aim of this study was to examine how MΦ metabolic reprogramming through FATP1 ablation affects the process of atherogenesis. We hypothesized that FATP1 limits MΦ-mediated inflammation during atherogenesis. Thus, mice lacking MΦ Fatp1 would display elevated formation of atherosclerotic lesions in a mouse model lacking the low-density lipoprotein (LDL) receptor (Ldlr

methodsWe transplanted bone marrow collected from Fatp1

resultsCompared to Fatp1

conclusionsMΦ Fatp1 limits atherogenesis and may be a viable target to metabolically reprogram MΦs.

Indexed as

Macrophage ActivationPlaque, AtheroscleroticAnimalsAortaAortic DiseasesAtherosclerosisBlood GlucoseBone Marrow TransplantationCells, CulturedCellular MicroenvironmentDisease Models, AnimalFatty Acid Transport ProteinsGenetic Predisposition to DiseaseInflammationLipidsMacrophages, PeritonealBlood GlucoseFatty Acid Transport ProteinsLipidsReceptors, LDLSlc27a1 protein, mouseFATP1Fatty acid transport proteinLDL receptorMacrophageMetabolic reprogram

Identifiers

PMID29035781
PMCPMC5705203
OpenAlexW2762789658

What OpenQuestion holds

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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.