Evidence map›Paper›PMID 33749877›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2021

Dermal fibroblast phagocytosis of apoptotic cells: A novel pathway for wound resolution.

Bruna Romana-Souza, Lin Chen, Trevor R Leonardo, Zhenlong Chen, Luisa A DiPietro

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.0field-weighted citation impact, top 27% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. More Than a Cleanup Crew: The Expanding Biology of Efferocytosis.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Review
  3. Review
  4. Loss of MFAP5 and Its Effect on Skin Homeostasis and Wound Healing.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  5. Article
  6. Article
  7. Apoptosis and Cell Clearance in Skin Wound Healing.Advances in experimental medicine and biology · 2025
    Review
  8. Efferocytosis in Homeostasis.Advances in experimental medicine and biology · 2025
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Angiogenesis in Wound Repair: Too Much of a Good Thing?Cold Spring Harbor perspectives in biology · 2022
    Review
  18. 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

5 authors at 2 institutions in 2 countries.

Bruna Romana-SouzaTissue Repair Laboratory, Rio de Janeiro State University, Rio de Janeiro, Rio de Janeiro, Brazil.ORCID 0000-0001-5665-8694
Lin ChenCenter for Wound Healing and Tissue Regeneration, University of Illinois at Chicago, Chicago, IL, USA.
Trevor R LeonardoDepartment of Microbiology and Immunology, College of Medicine, University of Illinois at Chicago, Chicago, IL, USA.
Zhenlong ChenDepartment of Anesthesiology, University of Illinois at Chicago, Chicago, IL, USA.
Luisa A DiPietroCenter for Wound Healing and Tissue Regeneration, University of Illinois at Chicago, Chicago, IL, USA.
University of Illinois Chicago · USUniversidade do Estado do Rio de Janeiro · BR

Funding

ANGIOGENESIS IN WOUND REPAIRR01GM050875 · NIGMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DIPIETRO, LUISA A · 1999 to 2020
$6.6M
Transcriptional Regulation of Wound Healing in Human Gingiva and SkinF31DE028747 · NIDCR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LEONARDO, TREVOR · 2019 to 2022
$183k
NIDCR NIH HHS F31 DE028747NIGMS NIH HHS R01 GM050875
6 · The paper itself

Abstract

The effective clearance of apoptotic cells is an essential step in the resolution of healing wounds. In particular, blood vessel regression during wound resolution produces a significant number of apoptotic endothelial cells (ApoEC) that must be cleared. In considering the fate of ApoEC and the presence of fibroblasts during wound resolution, we hypothesized that fibroblasts might serve as phagocytes involved in endothelial cell removal. The current study investigated whether dermal fibroblasts engulf ApoEC, whether this uptake alters the phenotype of dermal fibroblasts, and the biological molecules involved. In both in vitro and in vivo studies, following ApoEC engulfment, fibroblasts acquired a pro-healing phenotype (increased cell migration, contractility, α-smooth muscle actin expression, and collagen deposition). In addition, fibroblast uptake of ApoEC was shown to be mediated in part by the milk fat globule-EGF factor 8 protein/integrin α

Indexed as

AnimalsAntigens, SurfaceApoptosisEndothelial CellsFemaleGreen Fluorescent ProteinsHumansMiceMice, Inbred C57BLMilk ProteinsPhagocytosisReceptors, VitronectinSkinWound HealingAntigens, SurfaceGreen Fluorescent Proteinsintegrin alphaVbeta5Mfge8 protein, mouseMilk ProteinsReceptors, Vitronectinapoptosisendothelial cellfibroblastsmilk fat globule-EGF factor 8 proteinphagocytosiswound healing

Identifiers

PMID33749877
PMCPMC8670562
OpenAlexW3138063798

What OpenQuestion holds

Textmetadata
LicenceTDM
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.