Evidence map›Paper›PMID 35750773›Full record

ArticleNPJ Regenerative medicine2022

Proteoglycan 4 (PRG4) treatment enhances wound closure and tissue regeneration.

Roman J Krawetz, Saleem Abubacker, Catherine Leonard, Anand O Masson, Sophia Shah, Nadia Narendran, Pankaj Tailor, Suresh C Regmi, Elodie Labit, Nicoletta Ninkovic and 6 more

Open access · goldAbstract read
In one paragraph

Article in NPJ Regenerative medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 38 citations in OpenAlex.

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  11. Femur Shape Changes in Prg4-Deficient Mice: Morphological Insights Into Joint Well-Being.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  12. Review
  13. Biomedicines · 2025
    Review
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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

16 authors at 2 institutions in 2 countries.

Roman J KrawetzMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada. rkrawetz@ucalgary.ca.ORCID http://orcid.org/0000-0002-2576-4504
Saleem AbubackerMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Catherine LeonardMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Anand O MassonMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Sophia ShahMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Nadia NarendranMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Pankaj TailorMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Suresh C RegmiFaculty of Kinesiology, University of Calgary, Calgary, AB, Canada.
Elodie LabitDepartment of Comparative Biology and Experimental Medicine, University of Calgary, Calgary, AB, Canada.ORCID http://orcid.org/0000-0002-7659-6248
Nicoletta NinkovicMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Jessica May CorpuzMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Kenichi ItoDepartment of Biochemistry and Molecular Biology, University of Calgary, Calgary, AB, Canada.
T Michael UnderhillDepartment of Cellular and Physiological Sciences and Biomedical Research Centre, University of British Columbia, Vancouver, BC, Canada.ORCID http://orcid.org/0000-0003-3048-9102
Paul T SaloMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.ORCID http://orcid.org/0000-0002-4005-9758
Tannin A SchmidtMcCaig Institute for Bone & Joint Health, University of Calgary, Calgary, AB, Canada.
Jeff A BiernaskieDepartment of Comparative Biology and Experimental Medicine, University of Calgary, Calgary, AB, Canada.
University of Calgary · CAUniversity of British Columbia · CA

Funding

Calgary Foundation (CF) Grace Glaum ProfessorshipCanada Foundation for Innovation (Fondation canadienne pour l'innovation) JELFGouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) 01309MOP-311542-DIB-CBBA-170939Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (Conseil de Recherches en Sciences Naturelles et en Génie du Canada) RGPIN-2014-04586UCalgary | Cumming School of Medicine, University of Calgary (Cumming School of Medicine) PDF award
6 · The paper itself

Abstract

The wound healing response is one of most primitive and conserved physiological responses in the animal kingdom, as restoring tissue integrity/homeostasis can be the difference between life and death. Wound healing in mammals is mediated by immune cells and inflammatory signaling molecules that regulate tissue resident cells, including local progenitor cells, to mediate closure of the wound through formation of a scar. Proteoglycan 4 (PRG4), a protein found throughout the animal kingdom from fish to elephants, is best known as a glycoprotein that reduces friction between articulating surfaces (e.g. cartilage). Previously, PRG4 was also shown to regulate the inflammatory and fibrotic response. Based on this, we asked whether PRG4 plays a role in the wound healing response. Using an ear wound model, topical application of exogenous recombinant human (rh)PRG4 hastened wound closure and enhanced tissue regeneration. Our results also suggest that rhPRG4 may impact the fibrotic response, angiogenesis/blood flow to the injury site, macrophage inflammatory dynamics, recruitment of immune and increased proliferation of adult mesenchymal progenitor cells (MPCs) and promoting chondrogenic differentiation of MPCs to form the auricular cartilage scaffold of the injured ear. These results suggest that PRG4 has the potential to suppress scar formation while enhancing connective tissue regeneration post-injury by modulating aspects of each wound healing stage (blood clotting, inflammation, tissue generation and tissue remodeling). Therefore, we propose that rhPRG4 may represent a potential therapy to mitigate scar and improve wound healing.

Identifiers

PMID35750773
PMCPMC9232611
OpenAlexW4283382212

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.