Evidence map›Paper›PMID 33741914›Full record

ArticleNature communications2021

Recruited macrophages that colonize the post-inflammatory peritoneal niche convert into functionally divergent resident cells.

P A Louwe, L Badiola Gomez, H Webster, G Perona-Wright, C C Bain, S J Forbes, S J Jenkins

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed
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

83 citing papers in PubMed, 140 citations in OpenAlex.

  1. Review
  2. Macrophage heterogeneity in human secondary lymphoid organs.Clinical science (London, England : 1979) · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Depletion of CX3CR1Mucosal immunology · 2026
    Article
  10. Peritoneal cavity-derived GATA6Journal of advanced research · 2026
    Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article

23 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

7 authors at 3 institutions in 1 country.

P A LouweCentre for Inflammation Research, Queens Medical Research Institute, Edinburgh, EH16 4TJ, United Kingdom.ORCID 0000-0002-8451-1451
L Badiola GomezCentre for Inflammation Research, Queens Medical Research Institute, Edinburgh, EH16 4TJ, United Kingdom.ORCID 0000-0001-8961-134X
H WebsterInstitute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, G12 8TA, United Kingdom.
G Perona-WrightInstitute of Infection, Immunity & Inflammation, University of Glasgow, Glasgow, G12 8TA, United Kingdom.ORCID 0000-0003-2761-4275
C C BainCentre for Inflammation Research, Queens Medical Research Institute, Edinburgh, EH16 4TJ, United Kingdom.ORCID 0000-0001-8884-327X
S J ForbesCentre for Regenerative Medicine, University of Edinburgh, Edinburgh, EH16 4UU, United Kingdom.ORCID 0000-0003-3715-2561
S J JenkinsCentre for Inflammation Research, Queens Medical Research Institute, Edinburgh, EH16 4TJ, United Kingdom. stephen.jenkins@ed.ac.uk.ORCID 0000-0002-0233-5424
Centre for Inflammation Research · GBUniversity of Glasgow · GBMRC Centre for Regenerative Medicine · GB

Funding

Medical Research Council MR/K017047/1Medical Research Council MR/L008076/1Medical Research Council MR/S009779/1Wellcome TrustWellcome Trust 108906/Z/15/Z
6 · The paper itself

Abstract

Inflammation generally leads to recruitment of monocyte-derived macrophages. What regulates the fate of these cells and to what extent they can assume the identity and function of resident macrophages is unclear. Here, we show that macrophages elicited into the peritoneal cavity during mild inflammation persist long-term but are retained in an immature transitory state of differentiation due to the presence of enduring resident macrophages. By contrast, severe inflammation results in ablation of resident macrophages and a protracted phase wherein the cavity is incapable of sustaining a resident phenotype, yet ultimately elicited cells acquire a mature resident identity. These macrophages also have transcriptionally and functionally divergent features that result from inflammation-driven alterations to the peritoneal cavity micro-environment and, to a lesser extent, effects of origin and time-of-residency. Hence, rather than being predetermined, the fate of inflammation-elicited peritoneal macrophages seems to be regulated by the environment.

Indexed as

AnimalsCell DifferentiationCells, CulturedCytokinesFemaleGATA6 Transcription FactorGene Expression ProfilingInflammationMacrophagesMacrophages, PeritonealMaleMiceMice, CongenicMice, Inbred C57BLPeritoneal CavityPeritonitisCytokinesGata6 protein, mouseGATA6 Transcription Factor

Identifiers

PMID33741914
PMCPMC7979918
OpenAlexW3138784463

What OpenQuestion holds

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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.