Evidence map›Paper›PMID 32183071›Full record

ArticleInternational journal of molecular sciences2020

Ganglioside GM3 Up-Regulate Chondrogenic Differentiation by Transform Growth Factor Receptors.

Jae-Sung Ryu, Sang Young Seo, Eun-Jeong Jeong, Jong-Yeup Kim, Yong-Gon Koh, Yong Il Kim, Young-Kug Choo

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 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
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  7. Article
  8. Application of Mesenchymal Stem Cells in Inflammatory and Fibrotic Diseases.International journal of molecular sciences · 2020
    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

7 authors at 4 institutions in 1 country.

Jae-Sung RyuDepartment of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, Konyang University, Daejeon 35365, Korea.
Sang Young SeoDepartment of Biological Science, College of Natural Sciences, Wonkwang University, Iksan 54538, Korea.ORCID 0000-0002-7823-9295
Eun-Jeong JeongDepartment of Biological Science, College of Natural Sciences, Wonkwang University, Iksan 54538, Korea.
Jong-Yeup KimDepartment of Otorhinolaryngology-Head and Neck Surgery, College of Medicine, Konyang University, Daejeon 35365, Korea.
Yong-Gon KohCenter for Stem Cell & Arthritis Research, Department of Orthopaedic Surgery, Yonsei Sarang Hospital, Seoul 06698, Korea.
Yong Il KimDepartment of Stem Cell Research, TJC Life Research and Development Center, TJC Life, Seoul 08512, Korea.
Young-Kug ChooDepartment of Biological Science, College of Natural Sciences, Wonkwang University, Iksan 54538, Korea.
Konyang University · KRWonkwang University · KRKorea Research Institute of Bioscience and Biotechnology · KRYonsei Sarang Hospital · KR

Funding

Wonkwang University Wonkwang University in 2020
6 · The paper itself

Abstract

Mesenchymal stem cells, also known as multipotent stromal progenitor cells, can differentiate into cells of mesodermal lineage. Gangliosides are sialic acid-conjugated glycosphingolipids that are believed to regulate cell differentiation and several signaling molecules. These molecules are localized in glycosphingolipid-enriched microdomains on the cell surface and are regulated by glycosphingolipid composition. Transforming growth factor-beta (TGF-β) signaling plays a critical role in chondrogenic differentiation. However, the role of gangliosides in chondrogenesis is not understood. In this study, the relationship between the ganglioside GM3 and TGF-β activation, during chondrogenic differentiation, was investigated using an aggregate culture of human synovial membrane-derived mesenchymal stem cells. We showed that the gangliosides GM3 and GD3 were expressed after the chondrogenic differentiation of hSMSC aggregates. To test whether GM3 affected the chondrogenic differentiation of hSMSC aggregates, we used GM3 treatment during chondrogenic differentiation. The results showed that the group treated with 5 μM GM3 had higher expression of chondrogenic specific markers, increased toluidine blue, and safranin O staining, and increased accumulation of glycosaminoglycans compared with the untreated group. Furthermore, GM3 treatment enhanced TGF-β signaling via SMAD 2/3 during the chondrogenic differentiation of hSMSC aggregates. Taken together, our results suggested that GM3 may be useful in developing therapeutic agents for cell-based articular cartilage regeneration in articular cartilage disease.

Indexed as

Cell DifferentiationCells, CulturedChondrocytesChondrogenesisGlycosaminoglycansG(M3) GangliosideHumansMesenchymal Stem CellsReceptors, Transforming Growth Factor betaSignal TransductionSmad ProteinsSynovial MembraneTransforming Growth Factor betaUp-RegulationglucosaminoglycansGlycosaminoglycansG(M3) GangliosideReceptors, Transforming Growth Factor betaSmad ProteinsTransforming Growth Factor betachondrogenic aggregates differentiationgangliosideshuman synovial-derived mesenchymal stem cells

Identifiers

PMID32183071
PMCPMC7139639
OpenAlexW3011168301

What OpenQuestion holds

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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.