Evidence map›Paper›PMID 32306381›Full record

ArticleEuropean journal of immunology2020

Comprehensive characterization of myeloid cells during wound healing in healthy and healing-impaired diabetic mice.

Natasha Joshi, Lea Pohlmeier, Maya Ben-Yehuda Greenwald, Eric Haertel, Paul Hiebert, Manfred Kopf, Sabine Werner

Abstract read
In one paragraph

Article in European journal of immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
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

43 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Fibroblast-Mediated Macrophage Recruitment Supports Acute Wound Healing.The Journal of investigative dermatology · 2025
    Article
  7. Effect of ProbioticThe Malaysian journal of medical sciences : MJMS · 2025
    Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Apoptosis and Cell Clearance in Skin Wound Healing.Advances in experimental medicine and biology · 2025
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Cellular and molecular mechanisms of skin wound healing.Nature reviews. Molecular cell biology · 2024
    Review
  19. Article
  20. Targeting Grancalcin Accelerates Wound Healing by Improving Angiogenesis in Diabetes.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
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.

Natasha JoshiInstitute of Molecular Health Sciences, Department of Biology, ETH Zurich, Zurich, Switzerland.
Lea PohlmeierInstitute of Molecular Health Sciences, Department of Biology, ETH Zurich, Zurich, Switzerland.
Maya Ben-Yehuda GreenwaldInstitute of Molecular Health Sciences, Department of Biology, ETH Zurich, Zurich, Switzerland.
Eric HaertelInstitute of Molecular Health Sciences, Department of Biology, ETH Zurich, Zurich, Switzerland.
Paul HiebertInstitute of Molecular Health Sciences, Department of Biology, ETH Zurich, Zurich, Switzerland.
Manfred KopfInstitute of Molecular Health Sciences, Department of Biology, ETH Zurich, Zurich, Switzerland.
Sabine WernerInstitute of Molecular Health Sciences, Department of Biology, ETH Zurich, Zurich, Switzerland.ORCID 0000-0001-7397-8710

Funding

Swiss National Science Foundation 310030B_182829Swiss National Science Foundation 31003A_169204University Medicine Zurich
6 · The paper itself

Abstract

Wound healing involves the concerted action of various lymphoid and in particular myeloid cell populations. To characterize and quantitate different types of myeloid cells and to obtain information on their kinetics during wound healing, we performed multiparametric flow cytometry analysis. In healthy mice, neutrophil numbers increased early after injury and returned to near basal levels after completion of healing. Macrophages, monocyte-derived dendritic cells (DCs), and eosinophils were abundant throughout the healing phase, in particular in early wounds, and Langerhans cells increased after wounding and remained elevated after epithelial closure. Major differences in healing-impaired diabetic mice were a much higher percentage of immune cells in late wounds, mainly as a result of neutrophil, macrophage, and monocyte persistence; reduced numbers and percentages of macrophages and monocyte-derived DCs in early wounds; and of Langerhans cells, conventional DCs, and eosinophils throughout the healing process. Finally, unbiased cluster analysis (PhenoGraph) identified a large number of different clusters of myeloid cells in skin wounds. These results provide insight into myeloid cell diversity and dynamics during wound repair and highlight the abnormal inflammatory response associated with impaired healing.

Indexed as

AnimalsDiabetes ComplicationsDiabetes Mellitus, ExperimentalMice, Inbred C57BLMyeloid CellsWound HealingInflammationMyeloid cellSkinTissue repairWound healing

Identifiers

PMID32306381
PMCPMC7496577

What OpenQuestion holds

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Registered trials

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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.