Evidence map›Paper›PMID 26951856›Full record

ArticleInnate immunity2016

Changes in macrophage function modulated by the lipid environment.

Michael R Williams, David M Cauvi, Isabel Rivera, Dennis Hawisher, Antonio De Maio

Abstract read
In one paragraph

Article in Innate immunity, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Effects of Fasting on THP1 Macrophage Metabolism and Inflammatory Profile.International journal of molecular sciences · 2024
    Article
  2. Article
  3. Article
  4. Peroxisomes in host defense.PLoS pathogens · 2020
    Article
  5. Peroxisomes in Immune Response and Inflammation.International journal of molecular sciences · 2019
    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

5 authors.

Michael R WilliamsInitiative for Maximizing Student Development, University of California San Diego, La Jolla, CA, USA.
David M CauviDepartment of Surgery, University of California San Diego, La Jolla, CA, USA.
Isabel RiveraInitiative for Maximizing Student Development, University of California San Diego, La Jolla, CA, USA.
Dennis HawisherDepartment of Surgery, University of California San Diego, La Jolla, CA, USA.
Antonio De MaioDepartment of Surgery, University of California San Diego, La Jolla, CA, USA Department of Neurosciences, University of California San Diego, La Jolla, CA, USA Center for Investigations of Health and Education Disparities, University of California San Diego, La Jolla, CA, USA ademaio@ucsd.edu.

Funding

Mentoring Young Minds to Increase Diversity in the Biomedical ResearchR25GM083275 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DE MAIO, ANTONIO, LAWSON, MARK ANDREW · 2008 to 2022
$9.9M
Contribution of Cholesterol Homeostasis for Injury ResolutionR01GM114473 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DE MAIO, ANTONIO · 2015 to 2018
$1.2M
NIGMS NIH HHS GM083275NIGMS NIH HHS GM114473NIGMS NIH HHS R01 GM114473NIGMS NIH HHS R25 GM083275
6 · The paper itself

Abstract

Macrophages (Mφs) play a critical role in the defense against pathogens, orchestrating the inflammatory response during injury and maintaining tissue homeostasis. During these processes, macrophages encounter a variety of environmental conditions that are likely to change their gene expression pattern, which modulates their function. In this study, we found that murine Mφs displayed two different subpopulations characterized by differences in morphologies, expression of surface markers and phagocytic capacity under non-stimulated conditions. These two subpopulations could be recapitulated by changes in the culture conditions. Thus, Mφs grown in suspension in the presence of serum were highly phagocytic, whereas subtraction of serum resulted in rapid attachment and reduced phagocytic activity. The difference in phagocytosis between these subpopulations was correlated with the expression levels of FcγR. These two cell subpopulations also differed in their responses to LPS and the expression of surface markers, including CD14, CD86, scavenger receptor A1, TLR4 and low-density lipoprotein receptor. Moreover, we found that the lipid/cholesterol content in the culture medium mediated the differences between these two cell subpopulations. Thus, we described a mechanism that modulates Mφ function depending on the exposure to lipids within their surrounding microenvironment.

Indexed as

Cellular MicroenvironmentAnimalsB7-2 AntigenCell DifferentiationCell LineLipidsLipopolysaccharide ReceptorsLipopolysaccharidesMacrophagesMiceMice, Inbred StrainsPhagocytosisReceptors, IgGReceptors, ScavengerToll-Like Receptor 4B7-2 AntigenLipidsLipopolysaccharide ReceptorsLipopolysaccharidesReceptors, IgGReceptors, ScavengerToll-Like Receptor 4cholesterolHDLinflammationLDLlipidsMacrophagesreceptors

Identifiers

PMID26951856
PMCPMC5102337

What OpenQuestion holds

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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.