Evidence map›Paper›PMID 32992847›Full record

ArticleInternational journal of molecular sciences2020

Differential Production of Cartilage ECM in 3D Agarose Constructs by Equine Articular Cartilage Progenitor Cells and Mesenchymal Stromal Cells.

Stefanie Schmidt, Florencia Abinzano, Anneloes Mensinga, Jörg Teßmar, Jürgen Groll, Jos Malda, Riccardo Levato, Torsten Blunk

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. 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

8 authors at 3 institutions in 2 countries.

Stefanie SchmidtDepartment of Trauma, Hand, Plastic and Reconstructive Surgery, University of Würzburg, Oberdürrbacher Str. 6, 97080 Würzburg, Germany.
Florencia AbinzanoDepartment of Orthopedics, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands.ORCID 0000-0003-1382-0107
Anneloes MensingaDepartment of Orthopedics, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands.
Jörg TeßmarDepartment for Functional Materials in Medicine and Dentistry and Bavarian Polymer Institute, University of Würzburg, Pleicherwall 2, 97070 Würzburg, Germany.ORCID 0000-0001-7057-5369
Jürgen GrollDepartment for Functional Materials in Medicine and Dentistry and Bavarian Polymer Institute, University of Würzburg, Pleicherwall 2, 97070 Würzburg, Germany.ORCID 0000-0003-3167-8466
Jos MaldaDepartment of Orthopedics, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands.ORCID 0000-0002-9241-7676
Riccardo LevatoDepartment of Orthopedics, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands.
Torsten BlunkDepartment of Trauma, Hand, Plastic and Reconstructive Surgery, University of Würzburg, Oberdürrbacher Str. 6, 97080 Würzburg, Germany.
University of Würzburg · DEUniversity Medical Center Utrecht · NLUtrecht University · NL

Funding

Deutsche Forschungsgemeinschaft 326998133 (SFB TRR 225)Seventh Framework Programme 309962
6 · The paper itself

Abstract

Identification of articular cartilage progenitor cells (ACPCs) has opened up new opportunities for cartilage repair. These cells may be used as alternatives for or in combination with mesenchymal stromal cells (MSCs) in cartilage engineering. However, their potential needs to be further investigated, since only a few studies have compared ACPCs and MSCs when cultured in hydrogels. Therefore, in this study, we compared chondrogenic differentiation of equine ACPCs and MSCs in agarose constructs as monocultures and as zonally layered co-cultures under both normoxic and hypoxic conditions. ACPCs and MSCs exhibited distinctly differential production of the cartilaginous extracellular matrix (ECM). For ACPC constructs, markedly higher glycosaminoglycan (GAG) contents were determined by histological and quantitative biochemical evaluation, both in normoxia and hypoxia. Differential GAG production was also reflected in layered co-culture constructs. For both cell types, similar staining for type II collagen was detected. However, distinctly weaker staining for undesired type I collagen was observed in the ACPC constructs. For ACPCs, only very low alkaline phosphatase (ALP) activity, a marker of terminal differentiation, was determined, in stark contrast to what was found for MSCs. This study underscores the potential of ACPCs as a promising cell source for cartilage engineering.

Indexed as

ChondrogenesisTissue EngineeringAnimalsCartilage, ArticularCell DifferentiationCells, CulturedHorsesMesenchymal Stem CellsStem CellsACPCagarosecartilagechondroprogenitorsco-cultureECMhypoxiaMSCtissue engineeringzonal

Identifiers

PMID32992847
PMCPMC7582568
OpenAlexW3088047277

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.