Evidence map›Paper›PMID 35093449›Full record

ArticleGene2022

FGFR2 accommodates osteogenic cell fate determination in human mesenchymal stem cells.

Ying Zhang, Ling Ling, Arya Ajay D/O Ajayakumar, Yating Michelle Eio, Andre J van Wijnen, Victor Nurcombe, Simon M Cool

Open access · greenAbstract read
In one paragraph

Article in Gene, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  12. Role of FGF2 in promoting osteogenic differentiation for craniofacial bone regeneration.Regenerative engineering and translational medicine · 2025
    Article
  13. Article
  14. International journal of biological sciences · 2024
    Article
  15. 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

7 authors at 4 institutions in 2 countries.

Ying ZhangInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), 138673, Singapore.
Ling LingInstitute of Medical Biology, Agency for Science, Technology and Research (A*STAR), 138648, Singapore.
Arya Ajay D/O AjayakumarInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), 138673, Singapore.
Yating Michelle EioInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), 138673, Singapore.
Andre J van WijnenDepartment of Biochemistry, University of Vermont, Burlington, VT 05405, USA.
Victor NurcombeInstitute of Medical Biology, Agency for Science, Technology and Research (A*STAR), 138648, Singapore; Lee Kong Chian School of Medicine, Nanyang Technological University-Imperial College London, 636921, Singapore.
Simon M CoolInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research (A*STAR), 138673, Singapore; Department of Orthopaedic Surgery, Yong Loo Lin School of Medicine, National University of Singapore, 119288, Singapore. Electronic address: simon_cool@imcb.a-star.edu.sg.
Institute of Molecular and Cell Biology · SGAgency for Science, Technology and Research · SGNanyang Technological University · SGUniversity of Vermont · US

Funding

Molecular Control of Bone FormationR01AR049069 · NIAMS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WESTENDORF, JENNIFER J · 2003 to 2021
$5.8M
NIAMS NIH HHS R01 AR049069
6 · The paper itself

Abstract

The multilineage differentiation potential of human mesenchymal stem cells (hMSCs) underpins their clinical utility for tissue regeneration. Control of such cell-fate decisions is tightly regulated by different growth factors/cytokines and their cognate receptors. Fibroblast growth factors (FGFs) are among such factors critical for osteogenesis. However, how FGF receptors (FGFRs) help to orchestrate osteogenic progression remains to be fully elucidated. Here, we studied the protein levels of FGFRs during osteogenesis in human adult bone marrow-derived MSCs and discovered a positive correlation between FGFR2 expression and alkaline phosphatase (ALP) activity, an early marker of osteogenesis. Through RNA interference studies, we confirmed the role of FGFR2 in promoting the osteogenic differentiation of hMSCs. Knockdown of FGFR2 resulted in downregulation of pro-osteogenic genes and upregulation of pro-adipogenic genes and adipogenic commitment. Moreover, under osteogenic induction, FGFR2 knockdown resulted in upregulation of Enhancer of Zeste Homolog 2 (EZH2), an epigenetic enzyme that regulates MSC lineage commitment and suppresses osteogenesis. Lastly, we show that serial-passaged hMSCs have reduced FGFR2 expression and impaired osteogenic potential. Our study suggests that FGFR2 is critical for mediating osteogenic fate by regulating the balance of osteo-adipogenic lineage commitment. Therefore, examining FGFR2 levels during serial-passaging of hMSCs may prove useful for monitoring their multipotency.

Indexed as

Cell LineageAlkaline PhosphataseCell ProliferationCells, CulturedEnhancer of Zeste Homolog 2 ProteinGene Expression ProfilingGene Expression RegulationGene Knockdown TechniquesHumansMesenchymal Stem CellsOsteogenesisReceptor, Fibroblast Growth Factor, Type 1Receptor, Fibroblast Growth Factor, Type 2Alkaline PhosphataseEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanFGFR1 protein, humanFGFR2 protein, humanReceptor, Fibroblast Growth Factor, Type 1Receptor, Fibroblast Growth Factor, Type 2AdipogenesisEZH2FGFRLineage commitmentMesenchymal stem cellOsteogenesisPotency

Identifiers

PMID35093449
PMCPMC9256080
OpenAlexW4210781851

What OpenQuestion holds

Textmetadata
LicenceTDM
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.