Evidence map›Paper›PMID 28805694›Full record

ArticleInternational journal of molecular sciences2017

Progenitor Cells from Cartilage: Grade Specific Differences in Stem Cell Marker Expression.

Marija Mazor, Annabelle Cesaro, Mazen Ali, Thomas M Best, Eric Lespessaille, Hechmi Toumi

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Research advances in cartilage stem cells markers and induced differentiation.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2021
    Review
  9. Gene: X · 2020
    Article
  10. [Effects of cartilage progenitor cells and microRNA-140 on repair of osteoarthritic cartilage injury].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2019
    Review
  11. Article
  12. Article
  13. Review
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

6 authors at 3 institutions in 2 countries.

Marija MazorDepartment of Sciences, University of Orleans, I3MTO, EA 4708, Orleans F-45032, France. mazor.marica@gmail.com.
Annabelle CesaroDepartment of Sciences, University of Orleans, I3MTO, EA 4708, Orleans F-45032, France. annabelle.cesaro@univ-orleans.fr.
Mazen AliService chirurgie orthopédique et traumatologique Centre Hospitalier Régional d'Orléans, La Source 45000, France. mazen.ali@chr-orleans.fr.
Thomas M BestUHealth Sports Medicine Institute, Department of Orthopedics, Division of Sports Medicine, U of Miami, Coral Gables, FL 33146, USA. txb440@med.miami.edu.
Eric LespessailleDepartment of Sciences, University of Orleans, I3MTO, EA 4708, Orleans F-45032, France. eric.lespessailles@chr-orleans.fr.
Hechmi ToumiDepartment of Sciences, University of Orleans, I3MTO, EA 4708, Orleans F-45032, France. hechmi.toumi@chr-orleans.fr.
Université d'Orléans · FRCentre hospitalier universitaire d'Orléans · FRUniversity of Miami Health System · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent research has confirmed the presence of Mesenchymal stem cell (MSC)-like progenitors (MPC) in both normal and osteoarthritic cartilage. However, there is only limited information concerning how MPC markers are expressed with osteoarthritis (OA) progression. The purpose of this study was to compare the prevalence of various MPC markers in different OA grades. Human osteoarthritic tibial plateaus were obtained from ten patients undergoing total knee replacement. Each sample had been classified into a mild or severe group according to OARSI scoring. Tissue was taken from each specimen and mRNA expression levels of CD105, CD166, Notch 1, Sox9, Acan and Col II A1 were measured at day 0 and day 14 (2 weeks in vitro). Furthermore, MSC markers: Nucleostemin, CD90, CD73, CD166, CD105 and Notch 1 were studied by immunofluorescence. mRNA levels of MSC markers did not differ between mild and severe OA at day 0. At day 14, protein analysis showed that proliferated cells from both sources expressed all 6 MSC markers. Only cells from the mild OA subjects resulted in a significant increase of mRNA CD105 and CD166 after in vitro expansion. Moreover, cells from the mild OA subjects showed significantly higher levels of CD105, Sox9 and Acan compared with those from severe OA specimens. Results confirmed the presence of MSC markers in mild and severe OA tissue at both mRNA and protein levels. We found significant differences between cells obtained from mild compared to severe OA specimens suggests that mild OA derived cells may have a greater MSC potential.

Indexed as

Activated-Leukocyte Cell Adhesion MoleculeAgedAged, 80 and overAntigens, CDBiomarkersCartilage, ArticularCell Adhesion Molecules, NeuronalCell DifferentiationEndoglinFetal ProteinsHumansKnee JointMesenchymal Stem CellsMiddle AgedOsteoarthritis, KneeRNA, MessengerActivated-Leukocyte Cell Adhesion MoleculeALCAM protein, humanAntigens, CDBiomarkersCell Adhesion Molecules, NeuronalEndoglinENG protein, humanFetal ProteinsRNA, MessengerSOX9 protein, humanSOX9 Transcription Factorcartilagemesenchymal stem cell-like progenitorsosteoarthritic

Identifiers

PMID28805694
PMCPMC5578148
OpenAlexW2744978288

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.