Evidence map›Paper›PMID 23605563›Full record

ArticleStem cell reviews and reports2013

Wnt signaling behaves as a "master regulator" in the osteogenic and adipogenic commitment of human amniotic fluid mesenchymal stem cells.

Iolanda D'Alimonte, Angela Lannutti, Caterina Pipino, Pamela Di Tomo, Laura Pierdomenico, Eleonora Cianci, Ivana Antonucci, Marco Marchisio, Mario Romano, Liborio Stuppia and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Stem cell reviews and reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

62 citing papers in PubMed, 1 synthesis or guideline pooled it, 97 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  7. Article
  8. Article
  9. Review
  10. Article
  11. TCDD alters essential transcriptional regulators of osteogenic differentiation in multipotent mesenchymal stem cells.Toxicological sciences : an official journal of the Society of Toxicology · 2023
    Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. The roles and therapeutic approaches of MSC-derived exosomes in colorectal cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  18. Review
  19. Article
  20. Research progress on the application of framework nucleic acid in bone regeneration.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2021
    Article

2 more citing papers are in PubMed but not listed here.

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

13 authors at 1 institution in 1 country.

Iolanda D'AlimonteDepartment of Experimental and Clinical Sciences, University "G. D'Annunzio" of Chieti-Pescara, Chieti, Italy.
Angela Lannutti
Caterina Pipino
Pamela Di Tomo
Laura Pierdomenico
Eleonora Cianci
Ivana Antonucci
Marco Marchisio
Mario Romano
Liborio Stuppia
Francesco Caciagli
Assunta Pandolfi
Renata Ciccarelli
University of Chieti-Pescara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human amniotic fluid mesenchymal stem cells (huAFMSCs) are emerging as a promising therapeutic option in regenerative medicine. Here, we characterized huAFMSC phenotype and multipotentiality. When cultured in osteogenic medium, huAFMSC displayed a significant increase in: Alkaline Phosphatase (ALP) activity and mRNA expression, Alizarin Red S staining and Runx2 mRNA expression; whereas maintaining these cells in an adipogenic culture medium gave a time-dependent increase in PPARγ and FABP4 mRNA expression, glycerol-3-phosphate dehydrogenase (GPDH) activity and positivity to Oil Red Oil staining. These results confirm that huAFMSCs can differentiate toward osteogenic and adipogenic phenotypes. The canonical Wnt/ßcatenin signaling pathway appears to trigger huAFMSC osteoblastogenesis, since during early phases of osteogenic differentiation, the expression of Dishevelled-2 (Dvl-2), of the non-phosphorylated form of ß-catenin, and the phosphorylation of glycogen synthase kinase-3ß (GSK3ß) at serine 9 were upregulated. On the contrary, during adipogenic differentiation Dvl-2 expression decreased, whereas that of ß-catenin remained unchanged. This was associated with a late increase in GSK3ß phosphorylation. Consistent with this scenario, huAFMSCs exposure to Dickkopf-1, a selective inhibitor of the Wnt signaling, abolished Runx2 and ALP mRNA upregulation during huAFMSC osteogenic differentiation, whereas it enhanced FABP4 expression in adipocyte-differentiating cells. Taken together, these results unravel novel molecular determinants of huAFMSC commitment towards osteoblastogenesis, which may represent potential targets for directing the differentiation of these cells and improving their use in regenerative medicine.

Indexed as

Adaptor Proteins, Signal TransducingAdipogenesisAlkaline PhosphataseAmniotic Fluidbeta CateninBlotting, WesternCell DifferentiationCells, CulturedCore Binding Factor Alpha 1 SubunitDishevelled ProteinsFatty Acid-Binding ProteinsFemaleGene Expression Regulation, DevelopmentalGlycerolphosphate DehydrogenaseGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaAdaptor Proteins, Signal TransducingAlkaline Phosphatasebeta CateninCore Binding Factor Alpha 1 SubunitDishevelled ProteinsDKK1 protein, humanDVL2 protein, humanFABP4 protein, humanFatty Acid-Binding Proteinsglycerol-3-phosphate dehydrogenase, FAD-dependentGlycerolphosphate DehydrogenaseGlycogen Synthase Kinase 3Glycogen Synthase Kinase 3 betaIntercellular Signaling Peptides and ProteinsPhosphoproteinsPPAR gammaRUNX2 protein, human

Identifiers

PMID23605563
PMCPMC3785124
OpenAlexW1970482629

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.