Evidence map›Paper›PMID 35216203›Full record

ArticleInternational journal of molecular sciences2022

Gremlin-1 and BMP-4 Overexpressed in Osteoarthritis Drive an Osteochondral-Remodeling Program in Osteoblasts and Hypertrophic Chondrocytes.

Maria-Luisa Pérez-Lozano, Laure Sudre, Sandy van Eegher, Danièle Citadelle, Audrey Pigenet, Marie-Helène Lafage-Proust, Philippe Pastoureau, Frédéric De Ceuninck, Francis Berenbaum, Xavier Houard

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Review
  10. Osteoarthritis: pathogenic signaling pathways and therapeutic targets.Signal transduction and targeted therapy · 2023
    Review
  11. Article
  12. New perspective of skeletal stem cells.Biomaterials translational · 2022
    Review
  13. 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

10 authors at 2 institutions in 1 country.

Maria-Luisa Pérez-LozanoCentre de Recherche Saint-Antoine (CRSA), INSERM, Sorbonne Université, F-75012 Paris, France.ORCID 0000-0002-6473-3823
Laure SudreCentre de Recherche Saint-Antoine (CRSA), INSERM, Sorbonne Université, F-75012 Paris, France.
Sandy van EegherCentre de Recherche Saint-Antoine (CRSA), INSERM, Sorbonne Université, F-75012 Paris, France.
Danièle CitadelleCentre de Recherche Saint-Antoine (CRSA), INSERM, Sorbonne Université, F-75012 Paris, France.
Audrey PigenetCentre de Recherche Saint-Antoine (CRSA), INSERM, Sorbonne Université, F-75012 Paris, France.
Marie-Helène Lafage-ProustFaculté de Médecine, INSERM U1059, Université Jean Monnet, F-42270 Saint-Priest en Jarez, France.
Philippe PastoureauImmuno-Inflammatory Diseases Department, Servier Research Institute, F-92150 Suresnes, France.ORCID 0000-0002-0048-897X
Frédéric De CeuninckImmuno-Inflammatory Diseases Department, Servier Research Institute, F-92150 Suresnes, France.
Francis BerenbaumCentre de Recherche Saint-Antoine (CRSA), INSERM, Sorbonne Université, F-75012 Paris, France.
Xavier HouardCentre de Recherche Saint-Antoine (CRSA), INSERM, Sorbonne Université, F-75012 Paris, France.
Inserm · FRServier (France) · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is a whole joint disease characterized by an important remodeling of the osteochondral junction. It includes cartilage mineralization due to chondrocyte hypertrophic differentiation and bone sclerosis. Here, we investigated whether gremlin-1 (Grem-1) and its BMP partners could be involved in the remodeling events of the osteochondral junction in OA. We found that Grem-1, BMP-2, and BMP-4 immunostaining was detected in chondrocytes from the deep layer of cartilage and in subchondral bone of knee OA patients, and was positively correlated with cartilage damage. ELISA assays showed that bone released more Grem-1 and BMP-4 than cartilage, which released more BMP-2. In vitro experiments evidenced that compression stimulated the expression and the release of Grem-1 and BMP-4 by osteoblasts. Grem-1 was also overexpressed during the prehypertrophic to hypertrophic differentiation of murine articular chondrocytes. Recombinant Grem-1 stimulated Mmp-3 and Mmp-13 expression in murine chondrocytes and osteoblasts, whereas recombinant BMP-4 stimulated the expression of genes associated with angiogenesis (Angptl4 and osteoclastogenesis (Rankl and Ccl2). In conclusion, Grem-1 and BMP-4, whose expression at the osteochondral junction increased with OA progression, may favor the pathological remodeling of the osteochondral junction by inducing a catabolic and tissue remodeling program in hypertrophic chondrocytes and osteoblasts.

Indexed as

AnimalsBone Morphogenetic Protein 2Bone Morphogenetic Protein 4Cartilage, ArticularCell DifferentiationCell ProliferationChondrocytesChondrogenesisHumansIntercellular Signaling Peptides and ProteinsMatrix Metalloproteinase 13Matrix Metalloproteinase 3MiceMice, Inbred C57BLOsteoarthritis, KneeOsteoblastsBMP4 protein, humanBone Morphogenetic Protein 2Bone Morphogenetic Protein 4GREM1 protein, humanIntercellular Signaling Peptides and ProteinsMatrix Metalloproteinase 13Matrix Metalloproteinase 3Bmp-4gremlin-1hypertrophic chondrocytesmechanical stressosteoarthritisosteochondral remodeling

Identifiers

PMID35216203
PMCPMC8874623
OpenAlexW4213380653

What Socratic 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 Socratic graph.