Evidence map›Paper›PMID 36300892›Full record

ArticleAdvanced healthcare materials2023

An In Vitro Engineered Osteochondral Model as Tool to Study Osteoarthritis Environment.

Annachiara Scalzone, Giorgia Cerqueni, Xiao-Nong Wang, Ana Ferreira-Duarte, Kenny Dalgarno, Monica Mattioli-Belmonte, Piergiorgio Gentile

Open access · hybridAbstract read
In one paragraph

Article in Advanced healthcare materials, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Review
  3. Developing anFrontiers in immunology · 2025
    Article
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  6. Article
  7. Article
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  9. A cytokine-induced spheroid-basedFrontiers in bioengineering and biotechnology · 2023
    Article
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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

7 authors at 2 institutions in 2 countries.

Annachiara ScalzoneSchool of Engineering, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.ORCID 0000-0002-2354-8509
Giorgia CerqueniDepartment of Clinical and Molecular Sciences (DISCLIMO), Università Politecnica delle Marche, Ancona, 60126, Italy.ORCID 0000-0001-7390-7154
Xiao-Nong WangTranslational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.ORCID 0000-0003-1282-8799
Ana Ferreira-DuarteSchool of Engineering, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.ORCID 0000-0002-7728-1619
Kenny DalgarnoSchool of Engineering, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.
Monica Mattioli-BelmonteDepartment of Clinical and Molecular Sciences (DISCLIMO), Università Politecnica delle Marche, Ancona, 60126, Italy.ORCID 0000-0002-2087-2776
Piergiorgio GentileSchool of Engineering, Newcastle University, Newcastle upon Tyne, NE1 7RU, UK.ORCID 0000-0002-3036-6594
Newcastle University · GBMarche Polytechnic University · IT

Funding

Versus Arthritis 21156
6 · The paper itself

Abstract

Osteoarthritis (OA) is a joint degenerative pathology characterized by mechanical and inflammatory damages affecting synovium, articular cartilage (AC), and subchondral bone (SB). Several in vitro, in vivo, and ex vivo models are developed to study OA, but to date the identification of specific pharmacological targets seems to be hindered by the lack of models with predictive capabilities. This study reports the development of a biomimetic in vitro model of AC and SB interface. Gellan gum methacrylated and chondroitin sulfate/dopamine hydrogels are used for the AC portion, whereas polylactic acid functionalized with gelatin and nanohydroxyapatite for the SB. The physiological behavior of immortalized stem cells (Y201s) and Y201s differentiated in chondrocytes (Y201-Cs), respectively, for the SB and AC, is demonstrated over 21 days of culture in vitro in healthy and pathological conditions, whilst modeling the onset of cytokines-induced OA. The key metrics are: lower glycosaminoglycans production and increased calcification given by a higher Collagen X content, in the AC deep layer; higher expression of pro-angiogenic factor (vegf) and decreased expression of osteogenic markers (coll1, spp1, runx2) in the SB. This novel approach provides a new tool for studying the development and progression of OA.

Indexed as

Cartilage, ArticularOsteoarthritisBone and BonesChondrocytesHumansOsteogenesisTissue Engineeringchondroitin sulfate dopaminegellan gum methacrylatein vitro modelsosteoarthritisosteochondral unitproinflammatory mediators

Identifiers

PMID36300892
PMCPMC11481676
OpenAlexW4307425038

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.