Evidence map›Paper›PMID 24762537›Full record

ArticleScience (New York, N.Y.)2014

The transcription factor Gata6 links tissue macrophage phenotype and proliferative renewal.

Marcela Rosas, Luke C Davies, Peter J Giles, Chia-Te Liao, Bashar Kharfan, Timothy C Stone, Valerie B O'Donnell, Donald J Fraser, Simon A Jones, Philip R Taylor

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 239 papers.

0numbers the graph read from it
0cells of the map it votes in
239citing papers in PubMed
15.9field-weighted citation impact, top 1% 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

239 citing papers in PubMed, 363 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Article
  6. Human peritoneal CCR2Human cell · 2026
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  11. Article
  12. Article
  13. Review
  14. Review
  15. Liver macrophages: development, dynamics, and functions.Cellular & molecular immunology · 2025
    Review
  16. Review
  17. Article
  18. Review
  19. Article
  20. Tracing LYVE1bioRxiv : the preprint server for biology · 2025
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Marcela Rosas *Cardiff Institute of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Luke C Davies *Cardiff Institute of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Peter J GilesCentral Biotechnology Services, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Chia-Te LiaoCardiff Institute of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Bashar KharfanCardiff Institute of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Timothy C StoneCentral Biotechnology Services, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Valerie B O'DonnellCardiff Institute of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Donald J FraserInstitute of Molecular Medicine, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Simon A JonesCardiff Institute of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Philip R TaylorCardiff Institute of Infection and Immunity, Cardiff University School of Medicine, Heath Park, Cardiff, CF14 4XN, UK.
Cardiff University · GB

Funding

Medical Research Council G0601617Medical Research Council MR/J002151/1Medical Research Council MR/K02003X/1Wellcome Trust 094143
6 · The paper itself

Abstract

Tissue-resident macrophages are heterogeneous as a consequence of anatomical niche-specific functions. Many populations self-renew independently of bone marrow in the adult, but the molecular mechanisms of this are poorly understood. We determined a transcriptional profile for the major self-renewing population of peritoneal macrophages in mice. These cells specifically expressed the transcription factor Gata6. Selective deficiency of Gata6 in myeloid cells caused substantial alterations in the transcriptome of peritoneal macrophages. Gata6 deficiency also resulted in dysregulated peritoneal macrophage proliferative renewal during homeostasis and in response to inflammation, which was associated with delays in the resolution of inflammation. Our investigations reveal that the tissue macrophage phenotype is under discrete tissue-selective transcriptional control and that this is fundamentally linked to the regulation of their proliferation renewal.

Indexed as

Cell ProliferationAnimalsGATA6 Transcription FactorInflammationMacrophages, PeritonealMiceMice, KnockoutMyeloid CellsPhenotypeGata6 protein, mouseGATA6 Transcription Factor

Identifiers

PMID24762537
PMCPMC4185421
OpenAlexW2022485121

What OpenQuestion holds

Textmetadata
LicenceTDM
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.