Evidence map›Paper›PMID 23552798›Full record

ArticleThe Journal of investigative dermatology2013

Local arginase 1 activity is required for cutaneous wound healing.

Laura Campbell, Charis R Saville, Peter J Murray, Sheena M Cruickshank, Matthew J Hardman

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of investigative dermatology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed
13.9field-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

114 citing papers in PubMed, 245 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. The roles of arginases and arginine in immunity.Nature reviews. Immunology · 2025
    Review
  12. Review
  13. Article
  14. Macrophage energy metabolism in cardiometabolic disease.Molecular and cellular biochemistry · 2025
    Review
  15. Detrimental influence of Arginase-1 in infiltrating macrophages on poststroke functional recovery and inflammatory milieu.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review

54 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

5 authors at 3 institutions in 2 countries.

Laura CampbellThe Healing Foundation Centre, Faculty of Life Sciences, The University of Manchester, Manchester, UK.
Charis R SavilleThe Healing Foundation Centre, Faculty of Life Sciences, The University of Manchester, Manchester, UK.
Peter J MurrayDepartments of Infectious Diseases and Immunology, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
Sheena M CruickshankManchester Immunology Group, Faculty of Life Sciences, The University of Manchester, Manchester, UK.
Matthew J HardmanThe Healing Foundation Centre, Faculty of Life Sciences, The University of Manchester, Manchester, UK. Electronic address: matthew.j.hardman@manchester.ac.uk.
University of Manchester · GBLGBT Foundation · GBSt. Jude Children's Research Hospital · US

Funding

Medical Research Council G1000449
6 · The paper itself

Abstract

Chronic nonhealing wounds in the elderly population are associated with a prolonged and excessive inflammatory response, which is widely hypothesized to impede healing. Previous studies have linked alterations in local L-arginine metabolism, principally mediated by the enzymes arginase (Arg) and inducible nitric oxide synthase (iNOS), to pathological wound healing. Over subsequent years, interest in Arg/iNOS has focused on the classical versus alternatively activated (M1/M2) macrophage paradigm. Although the role of iNOS during healing has been studied, Arg contribution to healing remains unclear. Here, we report that Arg is dynamically regulated during acute wound healing. Pharmacological inhibition of local Arg activity directly perturbed healing, as did Tie2-cre-mediated deletion of Arg1, revealing the importance of Arg1 during healing. Inhibition or depletion of Arg did not alter alternatively activated macrophage numbers but instead was associated with increased inflammation, including increased influx of iNOS(+) cells and defects in matrix deposition. Finally, we reveal that in preclinical murine models reduced Arg expression directly correlates with delayed healing, and as such may represent an important future therapeutic target.

Indexed as

AnimalsArginaseDermatitisDisease Models, AnimalExtracellular MatrixFemaleMacrophagesMiceMice, Inbred C57BLMice, TransgenicNitric Oxide Synthase Type IIReceptor, TIE-2SkinWound HealingArg1 protein, mouseArginaseNitric Oxide Synthase Type IINos2 protein, mouseReceptor, TIE-2Tek protein, mouse

Identifiers

PMID23552798
PMCPMC3778883
OpenAlexW1981141014

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.