Evidence map›Paper›PMID 26154973›Full record

ArticleeLife2015

Identification of polarized macrophage subsets in zebrafish.

Mai Nguyen-Chi, Béryl Laplace-Builhe, Jana Travnickova, Patricia Luz-Crawford, Gautier Tejedor, Quang Tien Phan, Isabelle Duroux-Richard, Jean-Pierre Levraud, Karima Kissa, Georges Lutfalla and 2 more

Open access · goldAbstract read
In one paragraph

Article in eLife, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 163 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
163citing papers in PubMed, 1 pooled it
7.5field-weighted citation impact, top 2% 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

163 citing papers in PubMed, 1 synthesis or guideline pooled it, 300 citations in OpenAlex.

  1. Pooled it
  2. Review
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  7. Calcium Signaling in Macrophages During a Wound Response In Vivo.International journal of molecular sciences · 2026
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  17. Spatial microenvironments tune immune response dynamics in thebioRxiv : the preprint server for biology · 2025
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  20. Article

103 more citing papers are in PubMed but not listed here.

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

12 authors at 4 institutions in 1 country.

Mai Nguyen-ChiInstitut de Médecine Régénérative et Biothérapies, Institut national de la santé et de la recherche médicale, Montpellier, France.
Béryl Laplace-BuilheInstitut de Médecine Régénérative et Biothérapies, Institut national de la santé et de la recherche médicale, Montpellier, France.
Jana TravnickovaUniversité de Montpellier, Montpellier, France.
Patricia Luz-CrawfordInstitut de Médecine Régénérative et Biothérapies, Institut national de la santé et de la recherche médicale, Montpellier, France.
Gautier TejedorInstitut de Médecine Régénérative et Biothérapies, Institut national de la santé et de la recherche médicale, Montpellier, France.
Quang Tien PhanDynamique des Interactions Membranaires Normales et Pathologiques, Centre national de la recherche scientifique, Montpellier, France.
Isabelle Duroux-RichardInstitut de Médecine Régénérative et Biothérapies, Institut national de la santé et de la recherche médicale, Montpellier, France.
Jean-Pierre LevraudMacrophages et Développement de l'Immunité, Institut Pasteur, Paris, France.
Karima KissaUniversité de Montpellier, Montpellier, France.
Georges LutfallaUniversité de Montpellier, Montpellier, France.
Christian JorgensenInstitut de Médecine Régénérative et Biothérapies, Institut national de la santé et de la recherche médicale, Montpellier, France.
Farida DjouadInstitut de Médecine Régénérative et Biothérapies, Institut national de la santé et de la recherche médicale, Montpellier, France.
Université de Montpellier · FRInstitute for Regenerative Medicine & Biotherapy · FRLaboratory of Pathogens and Host Immunity · FRInstitut Pasteur · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While the mammalian macrophage phenotypes have been intensively studied in vitro, the dynamic of their phenotypic polarization has never been investigated in live vertebrates. We used the zebrafish as a live model to identify and trail macrophage subtypes. We generated a transgenic line whose macrophages expressing tumour necrosis factor alpha (tnfa), a key feature of classically activated (M1) macrophages, express fluorescent proteins Tg(mpeg1:mCherryF/tnfa:eGFP-F). Using 4D-confocal microscopy, we showed that both aseptic wounding and Escherichia coli inoculation triggered macrophage recruitment, some of which started to express tnfa. RT-qPCR on Fluorescence Activated Cell Sorting (FACS)-sorted tnfa(+) and tnfa(-) macrophages showed that they, respectively, expressed M1 and alternatively activated (M2) mammalian markers. Fate tracing of tnfa(+) macrophages during the time-course of inflammation demonstrated that pro-inflammatory macrophages converted into M2-like phenotype during the resolution step. Our results reveal the diversity and plasticity of zebrafish macrophage subsets and underline the similarities with mammalian macrophages proposing a new system to study macrophage functional dynamic.

Indexed as

AnimalsAnimals, Genetically ModifiedEscherichia coli InfectionsFlow CytometryGene Expression ProfilingGenes, ReporterMacrophagesMicroscopy, ConfocalMolecular Sequence DataReal-Time Polymerase Chain ReactionReverse Transcriptase Polymerase Chain ReactionSequence Analysis, DNATumor Necrosis Factor-alphaWounds and InjuriesZebrafishTumor Necrosis Factor-alphadevelopmental biologyimmunologylive imagingmacrophagesstem cellszebrafish

Identifiers

PMID26154973
PMCPMC4521581
OpenAlexW2156420692

What OpenQuestion holds

Textmetadata
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.