Evidence map›Paper›PMID 38975341›Full record

ArticleFrontiers in immunology2024

Generation of functionally active resident macrophages from adipose tissue by 3D cultures.

Adèle Arlat, Marie-Laure Renoud, Jean Nakhle, Miguel Thomas, Jessica Fontaine, Emmanuelle Arnaud, Cédric Dray, Hélène Authier, Paul Monsarrat, Agnès Coste and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

13 authors.

Adèle ArlatRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Marie-Laure RenoudRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Jean NakhleRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Miguel ThomasRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Jessica FontaineRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Emmanuelle ArnaudRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Cédric DrayRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Hélène AuthierRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Paul MonsarratRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Agnès CosteRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Louis CasteillaRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Marielle OussetRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.
Béatrice CousinRESTORE Research Center, Université de Toulouse, INSERM 1301, CNRS 5070, Etablissement Français du Sang (EFS), Ecole Nationale Vétérinaire de Touloue (ENVT), Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Within adipose tissue (AT), different macrophage subsets have been described, which played pivotal and specific roles in upholding tissue homeostasis under both physiological and pathological conditions. Nonetheless, studying resident macrophages Methods: Stroma-vascular cells isolated from murine subcutaneous AT were seeded on ultra-low adherent plates in the presence of macrophage colony-stimulating factor. After 4 days of culture, the cells spontaneously aggregate to form spheroids. A week later, macrophages begin to spread out of the spheroid and adhere to the culture plate. Results: This innovative three-dimensional (3D) culture method enables the generation of functional mature macrophages that present distinct genic and phenotypic characteristics compared to bone marrow-derived macrophages. They also show specific metabolic activity and polarization in response to stimulation, but similar phagocytic capacity. Additionally, based on single-cell analysis, AT-macrophages generated in 3D culture mirror the phenotypic and functional traits of Discussion: Our study describes a 3D

Indexed as

Adipose TissueCell Culture Techniques, Three DimensionalCell DifferentiationMacrophagesAnimalsCell Culture TechniquesCells, CulturedMiceMice, Inbred C57BLPhagocytosisPhenotypeSpheroids, Cellular3D cultureadipose tissuebone marrowmacrophage subpopulationmetabolismphagocytosisresident macrophageunsupervised analysis

Identifiers

PMID38975341
PMCPMC11224291

What OpenQuestion holds

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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.