Evidence map›Paper›PMID 29486196›Full record

ArticleDevelopmental cell2018

Fat Body Cells Are Motile and Actively Migrate to Wounds to Drive Repair and Prevent Infection.

Anna Franz, Will Wood, Paul Martin

Open access · hybridAbstract read
In one paragraph

Article in Developmental cell, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

58 citing papers in PubMed, 127 citations in OpenAlex.

  1. Article
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  13. Physical principles and mechanisms of cell migration.npj biological physics and mechanics · 2025
    Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Cellular and molecular mechanisms of skin wound healing.Nature reviews. Molecular cell biology · 2024
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Anna FranzSchool of Biochemistry, Biomedical Sciences, University of Bristol, Bristol BS8 1TD, UK.
Will WoodSchool of Cellular and Molecular Medicine, Biomedical Sciences, University of Bristol, Bristol BS8 1TD, UK. Electronic address: w.wood@ed.ac.uk.
Paul MartinSchool of Biochemistry, Biomedical Sciences, University of Bristol, Bristol BS8 1TD, UK; School of Physiology, Pharmacology and Neuroscience, Biomedical Sciences, University of Bristol, Bristol BS8 1TD, UK; School of Medicine, Cardiff University, Cardiff CF14 4XN, UK. Electronic address: paul.martin@bristol.ac.uk.
University of Bristol · GBCardiff University · GB

Funding

Medical Research Council MR/J002577/1Wellcome Trust
6 · The paper itself

Abstract

Adipocytes have many functions in various tissues beyond energy storage, including regulating metabolism, growth, and immunity. However, little is known about their role in wound healing. Here we use live imaging of fat body cells, the equivalent of vertebrate adipocytes in Drosophila, to investigate their potential behaviors and functions following skin wounding. We find that pupal fat body cells are not immotile, as previously presumed, but actively migrate to wounds using an unusual adhesion-independent, actomyosin-driven, peristaltic mode of motility. Once at the wound, fat body cells collaborate with hemocytes, Drosophila macrophages, to clear the wound of cell debris; they also tightly seal the epithelial wound gap and locally release antimicrobial peptides to fight wound infection. Thus, fat body cells are motile cells, enabling them to migrate to wounds to undertake several local functions needed to drive wound repair and prevent infections.

Indexed as

ActomyosinAdipocytesAnimalsAntimicrobial Cationic PeptidesCell MovementCells, CulturedDrosophila melanogasterEscherichia coliEscherichia coli InfectionsFat BodyWound HealingActomyosinAntimicrobial Cationic Peptidesadipocytesantimicrobial peptides (AMPs)cell migrationDrosophilafat bodyhemocytesinflammatory responsewound healingwound infection

Identifiers

PMID29486196
PMCPMC6113741
OpenAlexW2788619667

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.