Evidence map›Paper›PMID 32433527›Full record

ArticleScientific reports2020

Transforming growth factor-beta stimulates human bone marrow-derived mesenchymal stem/stromal cell chondrogenesis more so than kartogenin.

E Music, T J Klein, W B Lott, M R Doran

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

17 citing papers in PubMed, 27 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

E MusicQueensland University of Technology (QUT), Centre for Biomedical Technologies (CBT), School of Biomedical Sciences, Faculty of Health, Institute of Health and Biomedical Innovation (IHBI), Brisbane, Australia.
T J KleinQueensland University of Technology (QUT), Centre for Biomedical Technologies (CBT), School of Mechanical, Medical and Process Engineering, Faculty of Science and Engineering, Institute of Health and Biomedical Innovation, Brisbane, Australia, Institute of Health and Biomedical Innovation (IHBI), Brisbane, Australia.
W B LottQueensland University of Technology (QUT), Centre for Biomedical Technologies (CBT), School of Biomedical Sciences, Faculty of Health, Institute of Health and Biomedical Innovation (IHBI), Brisbane, Australia.
M R DoranQueensland University of Technology (QUT), Centre for Biomedical Technologies (CBT), School of Biomedical Sciences, Faculty of Health, Institute of Health and Biomedical Innovation (IHBI), Brisbane, Australia. michael.doran@qut.edu.au.
Queensland University of Technology · AUTranslational Research Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A previous study identified kartogenin (KGN) as a potent modulator of bone marrow mesenchymal stem/stromal cell (BMSC) chondrogenesis. This initial report did not contrast KGN directly against transforming growth factor-beta 1 (TGF-β1), the most common growth factor used in chondrogenic induction medium. Herein, we directly compared the in vitro chondrogenic potency of TGF-β1 and KGN using a high resolution micropellet model system. Micropellets were cultured for 7-14 days in medium supplemented with TGF-β1, KGN, or both TGF-β1 + KGN. Following 14 days of induction, micropellets exposed to TGF-β1 alone or TGF-β1 + KGN in combination were larger and produced more glycosominoglycan (GAG) than KGN-only cultures. When TGF-β1 + KGN was used, GAG quantities were similar or slightly greater than the TGF-β1-only cultures, depending on the BMSC donor. BMSC micropellet cultures supplemented with KGN alone contracted in size over the culture period and produced minimal GAG. Indicators of hypertrophy were not mitigated in TGF-β1 + KGN cultures, suggesting that KGN does not obstruct BMSC hypertrophy. KGN appears to have weak chondrogenic potency in human BMSC cultures relative to TGF-β1, does not obstruct hypertrophy, and may not be a viable alternative to growth factors in cartilage tissue engineering.

Indexed as

AnilidesCartilageCell DifferentiationCells, CulturedChondrogenesisCulture MediaHumansMesenchymal Stem CellsPhthalic AcidsPrimary Cell CultureRecombinant ProteinsTissue EngineeringTransforming Growth Factor beta1AnilidesCulture MediakartogeninPhthalic AcidsRecombinant ProteinsTGFB1 protein, humanTransforming Growth Factor beta1

Identifiers

PMID32433527
PMCPMC7239921
OpenAlexW3026659401

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.