Evidence map›Paper›PMID 37024468›Full record

ArticleNature communications2023

Tryptase β regulation of joint lubrication and inflammation via proteoglycan-4 in osteoarthritis.

Nabangshu Das, Luiz G N de Almeida, Afshin Derakhshani, Daniel Young, Kobra Mehdinejadiani, Paul Salo, Alexander Rezansoff, Gregory D Jay, Christian P Sommerhoff, Tannin A Schmidt and 2 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
13.4field-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

36 citing papers in PubMed, 54 citations in OpenAlex.

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  18. Supramolecular Lubricating Hydrogel Microspheres Reshape Damaged Matrix Regeneration.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  19. Article
  20. Prx1NPJ Regenerative medicine · 2025
    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

12 authors at 3 institutions in 3 countries.

Nabangshu DasFaculty of Kinesiology, University of Calgary, Calgary, AB, Canada.
Luiz G N de AlmeidaHotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Afshin DerakhshaniHotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Daniel YoungHotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Kobra MehdinejadianiHotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Paul SaloMcCaig Institute for Bone and Joint Health, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.ORCID 0000-0002-4005-9758
Alexander RezansoffFaculty of Kinesiology, University of Calgary, Calgary, AB, Canada.
Gregory D JayDepartment of Emergency Medicine, Warren Alpert Medical School & School of Engineering, Brown University, Providence, RI, USA.
Christian P SommerhoffInstitute of Medical Education and Institute of Laboratory Medicine, University Hospital, LMU Munich, Munich, Germany.
Tannin A SchmidtMcCaig Institute for Bone and Joint Health, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Roman KrawetzMcCaig Institute for Bone and Joint Health, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada. rkrawetz@ucalgary.ca.ORCID 0000-0002-2576-4504
Antoine DufourFaculty of Kinesiology, University of Calgary, Calgary, AB, Canada. antoine.dufour@ucalgary.ca.ORCID 0000-0002-3429-4188
University of Calgary · CABrown University · USLudwig-Maximilians-Universität München · DE

Funding

CIHR 449589
6 · The paper itself

Abstract

PRG4 is an extracellular matrix protein that maintains homeostasis through its boundary lubricating and anti-inflammatory properties. Altered expression and function of PRG4 have been associated with joint inflammatory diseases, including osteoarthritis. Here we show that mast cell tryptase β cleaves PRG4 in a dose- and time-dependent manner, which was confirmed by silver stain gel electrophoresis and mass spectrometry. Tryptase-treated PRG4 results in a reduction of lubrication. Compared to full-length, cleaved PRG4 further activates NF-κB expression in cells overexpressing TLR2, -4, and -5. In the destabilization of the medial meniscus model of osteoarthritis in rat, tryptase β and PRG4 colocalize at the site of injury in knee cartilage and is associated with disease severity. When human primary synovial fibroblasts from male osteoarthritis patients or male healthy subjects treated with tryptase β and/or PRG4 are subjected to a quantitative shotgun proteomics and proteome changes are characterized, it further supports the role of NF-κB activation. Here we show that tryptase β as a modulator of joint lubrication in osteoarthritis via the cleavage of PRG4.

Indexed as

Cartilage, ArticularOsteoarthritisAnimalsHumansInflammationLubricationMaleNF-kappa BProteoglycansRatsTryptasesNF-kappa BProteoglycansTryptases

Identifiers

PMID37024468
PMCPMC10079686
OpenAlexW4362667191

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.