Evidence map›Paper›PMID 38679735›Full record

ArticleStem cell research & therapy2024

rhBMP-2 induces terminal differentiation of human bone marrow mesenchymal stromal cells only by synergizing with other signals.

Neda Kathami, Carolina Moreno-Vicente, Pablo Martín, Jhonatan A Vergara-Arce, Raquel Ruiz-Hernández, Daniela Gerovska, Ana M Aransay, Marcos J Araúzo-Bravo, Sandra Camarero-Espinosa, Ander Abarrategi

Abstract read
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Article in Stem cell research & therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

4 citing papers in PubMed.

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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

10 authors.

Neda Kathami *Center for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), 20014, Donostia-San Sebastian, Spain.
Carolina Moreno-Vicente *Complutense University of Madrid, 28040, Madrid, Spain.
Pablo MartínCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), 20014, Donostia-San Sebastian, Spain.
Jhonatan A Vergara-ArceCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), 20014, Donostia-San Sebastian, Spain.
Raquel Ruiz-HernándezCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), 20014, Donostia-San Sebastian, Spain.
Daniela GerovskaComputational Biology and Systems Biomedicine, Biodonostia Health Research Institute, 20014, San Sebastián, Spain.
Ana M AransayCenter for Cooperative Research in Biosciences (CIC bioGUNE), Basque Research and Technology Alliance (BRTA), 48160, Derio, Spain.
Marcos J Araúzo-BravoComputational Biology and Systems Biomedicine, Biodonostia Health Research Institute, 20014, San Sebastián, Spain.
Sandra Camarero-EspinosaPOLYMAT, University of the Basque Country (UPV-EHU), 20018, Donostia-San Sebastian, Spain.
Ander AbarrategiCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology Alliance (BRTA), 20014, Donostia-San Sebastian, Spain. aabarrategi@cicbiomagune.es.ORCID 0000-0002-6510-2337

Funding

Agencia Estatal de Investigación PID2020-114901RA-I00Agencia Estatal de Investigación PID2020-119715GB-I00Agencia Estatal de Investigación PID2021-127191OB-I00Agencia Estatal de Investigación PRE2018-084542Agencia Estatal de Investigación RTI2018-101708-A-I00Agencia Estatal de Investigación RYC2018-025502-IEuskal Herriko Unibertsitatea GIU21/033-EH2020 European Research Council 899417
6 · The paper itself

Abstract

backgroundRecombinant human bone morphogenetic protein 2 (rhBMP-2) and human bone marrow mesenchymal stromal cells (hBM-MSCs) have been thoroughly studied for research and translational bone regeneration purposes. rhBMP-2 induces bone formation in vivo, and hBM-MSCs are its target, bone-forming cells. In this article, we studied how rhBMP-2 drives the multilineage differentiation of hBM-MSCs both in vivo and in vitro.

methodsrhBMP-2 and hBM-MSCs were tested in an in vivo subcutaneous implantation model to assess their ability to form mature bone and undergo multilineage differentiation. Then, the hBM-MSCs were treated in vitro with rhBMP-2 for short-term or long-term cell-culture periods, alone or in combination with osteogenic, adipogenic or chondrogenic media, aiming to determine the role of rhBMP-2 in these differentiation processes.

resultsThe data indicate that hBM-MSCs respond to rhBMP-2 in the short term but fail to differentiate in long-term culture conditions; these cells overexpress the rhBMP-2 target genes DKK1, HEY-1 and SOST osteogenesis inhibitors. However, in combination with other differentiation signals, rhBMP-2 acts as a potentiator of multilineage differentiation, not only of osteogenesis but also of adipogenesis and chondrogenesis, both in vitro and in vivo.

conclusionsAltogether, our data indicate that rhBMP-2 alone is unable to induce in vitro osteogenic terminal differentiation of hBM-MSCs, but synergizes with other signals to potentiate multiple differentiation phenotypes. Therefore, rhBMP-2 triggers on hBM-MSCs different specific phenotype differentiation depending on the signalling environment.

Indexed as

Bone Morphogenetic Protein 2Cell DifferentiationMesenchymal Stem CellsOsteogenesisRecombinant ProteinsAdipogenesisBone Marrow CellsCells, CulturedChondrogenesisHumansSignal TransductionTransforming Growth Factor betaBone Morphogenetic Protein 2recombinant human bone morphogenetic protein-2Recombinant ProteinsTransforming Growth Factor betaAdipogenesisChondrogenesisDifferentiationMesenchymal stem cellsOsteogenesisrhBMP-2

Identifiers

PMID38679735
PMCPMC11057131

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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.