Evidence map›Paper›PMID 30674726›Full record

ArticleJCI insight2019

Systems genetics identifies a macrophage cholesterol network associated with physiological wound healing.

Marta Bagnati, Aida Moreno-Moral, Jeong-Hun Ko, Jérôme Nicod, Nathan Harmston, Martha Imprialou, Laurence Game, Jesus Gil, Enrico Petretto, Jacques Behmoaras

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Macrophages: sentinels, warriors, and healers.Human molecular genetics · 2025
    Review
  3. Article
  4. Article
  5. Decoding the role of macrophages in periodontitis and type 2 diabetes using single-cell RNA-sequencing.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  6. Article
  7. Macrophage-mediated inflammation in diabetic wound repair.Seminars in cell & developmental biology · 2021
    Review
  8. Fragile GeneFrontiers in oncology · 2021
    Article
  9. Article
  10. Article
  11. 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

10 authors at 4 institutions in 2 countries.

Marta BagnatiCentre for Inflammatory Disease, Imperial College London, Hammersmith Hospital, London, United Kingdom (UK).
Aida Moreno-MoralDuke-NUS Medical School, Singapore, Singapore.
Jeong-Hun KoCentre for Inflammatory Disease, Imperial College London, Hammersmith Hospital, London, United Kingdom (UK).
Jérôme NicodWellcome Centre for Human Genetics, University of Oxford, Oxford, UK.
Nathan HarmstonDuke-NUS Medical School, Singapore, Singapore.
Martha ImprialouCentre for Inflammatory Disease, Imperial College London, Hammersmith Hospital, London, United Kingdom (UK).
Laurence GameGenomics Laboratory, Medical Research Council (MRC) London Institute of Medical Sciences, Imperial College London, Hammersmith Hospital, London, UK.
Jesus GilCell Proliferation Group, MRC London Institute of Medical Sciences (LMS), London, UK.
Enrico PetrettoDuke-NUS Medical School, Singapore, Singapore.
Jacques BehmoarasCentre for Inflammatory Disease, Imperial College London, Hammersmith Hospital, London, United Kingdom (UK).
Hammersmith Hospital · GBDuke-NUS Medical School · SGCentre for Human Genetics · GBMRC London Institute of Medical Sciences · GB

Funding

Medical Research Council MC_U120085810Medical Research Council MC_U120097112Medical Research Council MR/M004716/1Medical Research Council MR/N01121X/1
6 · The paper itself

Abstract

Among other cells, macrophages regulate the inflammatory and reparative phases during wound healing but genetic determinants and detailed molecular pathways that modulate these processes are not fully elucidated. Here, we took advantage of normal variation in wound healing in 1,378 genetically outbred mice, and carried out macrophage RNA-sequencing profiling of mice with extreme wound healing phenotypes (i.e., slow and fast healers, n = 146 in total). The resulting macrophage coexpression networks were genetically mapped and led to the identification of a unique module under strong trans-acting genetic control by the Runx2 locus. This macrophage-mediated healing network was specifically enriched for cholesterol and fatty acid biosynthetic processes. Pharmacological blockage of fatty acid synthesis with cerulenin resulted in delayed wound healing in vivo, and increased macrophage infiltration in the wounded skin, suggesting the persistence of an unresolved inflammation. We show how naturally occurring sequence variation controls transcriptional networks in macrophages, which in turn regulate specific metabolic pathways that could be targeted in wound healing.

Indexed as

CholesterolDermatologyInflammationMacrophages

Identifiers

PMID30674726
PMCPMC6413785
OpenAlexW2913589053

What OpenQuestion holds

Textmetadata
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.