Evidence map›Paper›PMID 37681409›Full record

ArticleJCI insight2023

Adult Prg4+ progenitors repair long-term articular cartilage wounds in vivo.

Mei Massengale, Justin L Massengale, Catherine R Benson, Ninib Baryawno, Toshihiko Oki, Matthew L Steinhauser, Alissa Wang, Deepak Balani, Luke S Oh, Mark A Randolph and 3 more

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Mastication-Induced Electrical Stimulation Activates Prg4Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  6. Stage-resolved geography of mouse skeletal stem cells.Journal of bone and mineral metabolism · 2026
    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

13 authors at 4 institutions in 1 country.

Mei MassengaleSpaulding Rehabilitation Network at Mass General Brigham, Cambridge, Massachusetts, USA.
Justin L MassengaleDepartment of Neurosurgery, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Catherine R BensonDepartment of Medicine, Endocrine Unit, and.
Ninib BaryawnoCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Toshihiko OkiCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Matthew L SteinhauserAging Institute, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.
Alissa WangDepartment of Medicine, Endocrine Unit, and.
Deepak BalaniDepartment of Medicine, Endocrine Unit, and.
Luke S OhDepartment of Orthopedic Surgery, and.
Mark A RandolphDepartment of Plastic Surgery, Massachusetts General Hospital, Boston, Massachusetts, USA.
Thomas J GillDepartment of Stem Cell and Regenerative Biology, Harvard University, Cambridge, Massachusetts, USA.
Henry M KronenbergDepartment of Medicine, Endocrine Unit, and.
David T ScaddenCenter for Regenerative Medicine, Massachusetts General Hospital, Boston, Massachusetts, USA.
Harvard University · USBeth Israel Deaconess Medical Center · USBrigham and Women's Hospital · USMassachusetts General Hospital · US

Funding

Tissue Phenotyping CoreP01DK011794 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MANNSTADT, MICHAEL · 1986 to 2023
$44.4M
Joint Biology Consortium Resource-based CenterP30AR070253 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Peter A Nigrovic, Jeffrey Andrew Sparks · 2016 to 2026
$9.4M
The role of the osteocyte in responses to osteoporosis anabolic treatment in humans and miceP50AR080596 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI Marc Nathan Wein · 2023 to 2026
$7.4M
Skeletal Phenotyping CoreP30AR066261 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI KRONENBERG, HENRY M. · 2014 to 2018
$3.5M
NIAMS NIH HHS P30 AR066261NIAMS NIH HHS P30 AR070253NIAMS NIH HHS P50 AR080596NIDDK NIH HHS P01 DK011794
6 · The paper itself

Abstract

The identity and origin of the stem/progenitor cells for adult joint cartilage repair remain unknown, impeding therapeutic development. Simulating the common therapeutic modality for cartilage repair in humans, i.e., full-thickness microfracture joint surgery, we combined the mouse full-thickness injury model with lineage tracing and identified a distinct skeletal progenitor cell type enabling long-term (beyond 7 days after injury) articular cartilage repair in vivo. Deriving from a population with active Prg4 expression in adulthood while lacking aggrecan expression, these progenitors proliferate, differentiate to express aggrecan and type II collagen, and predominate in long-term articular cartilage wounds, where they represent the principal repair progenitors in situ under native repair conditions without cellular transplantation. They originate outside the adult bone marrow or superficial zone articular cartilage. These findings have implications for skeletal biology and regenerative medicine for joint injury repair.

Indexed as

Cartilage, ArticularAdultAggrecansAnimalsCollagen Type IIDisease Models, AnimalHumansMiceProteoglycan 4ProteoglycansStem CellsAggrecansCollagen Type IIPrg4 protein, mouseProteoglycan 4ProteoglycansAdult stem cellsBone marrowCartilageCell Biology

Identifiers

PMID37681409
PMCPMC10544199
OpenAlexW4386523184

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.