Evidence map›Paper›PMID 34529238›Full record

ArticleEndocrine2022

A novel in vitro assay to study chondrocyte-to-osteoblast transdifferentiation.

Miriam E A Tschaffon, Stefan O Reber, Astrid Schoppa, Sayantan Nandi, Ion C Cirstea, Attila Aszodi, Anita Ignatius, Melanie Haffner-Luntzer

Open access · hybridAbstract read
In one paragraph

Article in Endocrine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

12 citing papers in PubMed, 11 citations in OpenAlex.

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  6. International journal of molecular sciences · 2025
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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 1 institution in 1 country.

Miriam E A TschaffonInstitute of Orthopedic Research and Biomechanics, University Medical Center Ulm, Ulm, Germany.ORCID http://orcid.org/0000-0002-6409-9340
Stefan O ReberLaboratory for Molecular Psychosomatics, Department of Psychosomatic Medicine and Psychotherapy, University of Ulm, Ulm, Germany.
Astrid SchoppaInstitute of Orthopedic Research and Biomechanics, University Medical Center Ulm, Ulm, Germany.
Sayantan NandiInstitute of Comparative Molecular Endocrinology, University of Ulm, Ulm, Germany.
Ion C CirsteaInstitute of Comparative Molecular Endocrinology, University of Ulm, Ulm, Germany.
Attila AszodiLaboratory of Experimental Surgery and Regenerative Medicine, Clinic for General, Trauma and Reconstructive Surgery, Klinikum der Universität München, Martinsried, Germany.
Anita IgnatiusInstitute of Orthopedic Research and Biomechanics, University Medical Center Ulm, Ulm, Germany.
Melanie Haffner-LuntzerInstitute of Orthopedic Research and Biomechanics, University Medical Center Ulm, Ulm, Germany. melanie.haffner-luntzer@uni-ulm.de.
Universität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeEndochondral ossification, which involves transdifferentiation of chondrocytes into osteoblasts, is an important process involved in the development and postnatal growth of most vertebrate bones as well as in bone fracture healing. To study the basic molecular mechanisms of this process, a robust and easy-to-use in vitro model is desirable. Therefore, we aimed to develop a standardized in vitro assay for the transdifferentiation of chondrogenic cells towards the osteogenic lineage.

methodsMurine chondrogenic ATDC5 cells were differentiated into the chondrogenic lineage for seven days and subsequently differentiated towards the osteogenic direction. Gene expression analysis of pluripotency, as well as chondrogenic and osteogenic markers, cell-matrix staining, and immunofluorescent staining, were performed to assess the differentiation. In addition, the effects of Wnt3a and lipopolysaccharides (LPS) on the transdifferentiation were tested by their addition to the osteogenic differentiation medium.

resultsFollowing osteogenic differentiation, chondrogenically pe-differentiated cells displayed the expression of pluripotency and osteogenic marker genes as well as alkaline phosphatase activity and a mineralized matrix. Co-expression of Col2a1 and Col1a1 after one day of osteogenic differentiation indicated that osteogenic cells had differentiated from chondrogenic cells. Wnt3a increased and LPS decreased transdifferentiation towards the osteogenic lineage.

conclusionWe successfully established a rapid, standardized in vitro assay for the transdifferentiation of chondrogenic cells into osteogenic cells, which is suitable for testing the effects of different compounds on this cellular process.

Indexed as

ChondrocytesOsteogenesisAnimalsCell DifferentiationCells, CulturedCell TransdifferentiationChondrogenesisMiceOsteoblastsCartilage to bone transformationChondrocyteEndochondral ossificationFracture healingIn vitro assayTransdifferentiation

Identifiers

PMID34529238
PMCPMC8763722
OpenAlexW3199240907

What OpenQuestion holds

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Registered trials

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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.