Evidence map›Paper›PMID 32899269›Full record

ArticleInternational journal of molecular sciences2020

Immobilization of BMP-2 and VEGF within Multilayered Polydopamine-Coated Scaffolds and the Resulting Osteogenic and Angiogenic Synergy of Co-Cultured Human Mesenchymal Stem Cells and Human Endothelial Progenitor Cells.

Maria Godoy-Gallardo, Núria Portolés-Gil, Ana M López-Periago, Concepción Domingo, Leticia Hosta-Rigau

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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

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  7. Reasoning on Pore Terminology in 3D Bioprinting.Gels (Basel, Switzerland) · 2024
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  18. Advances in Growth Factor Delivery for Bone Tissue Engineering.International journal of molecular sciences · 2021
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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

5 authors at 2 institutions in 2 countries.

Maria Godoy-GallardoDepartment of Health Technology, Centre for Nanomedicine and Theranostics, DTU Health Tech, Technical University of Denmark, Produktionstorvet, Building 423, 2800 Kgs. Lyngby, Denmark.ORCID 0000-0002-7232-3998
Núria Portolés-GilMaterials Science Institute of Barcelona (ICMAB-CSIC), Campus de la UAB s/n, 08193 Bellaterra, Spain.ORCID 0000-0002-2580-4641
Ana M López-PeriagoMaterials Science Institute of Barcelona (ICMAB-CSIC), Campus de la UAB s/n, 08193 Bellaterra, Spain.ORCID 0000-0002-3777-3205
Concepción DomingoMaterials Science Institute of Barcelona (ICMAB-CSIC), Campus de la UAB s/n, 08193 Bellaterra, Spain.ORCID 0000-0002-6976-8283
Leticia Hosta-RigauDepartment of Health Technology, Centre for Nanomedicine and Theranostics, DTU Health Tech, Technical University of Denmark, Produktionstorvet, Building 423, 2800 Kgs. Lyngby, Denmark.ORCID 0000-0001-8177-4806
Institut de Ciència de Materials de Barcelona · ESTechnical University of Denmark · DK

Funding

Lundbeckfonden R163-2013- 15402Spanish MEC, Severo Ochoa Program SEV-2015-0496Teknologi og Produktion, Det Frie Forskningsråd 6111-00298B
6 · The paper itself

Abstract

We have previously reported the fabrication of a polycaprolactone and hydroxyapatite composite scaffold incorporating growth factors to be used for bone regeneration. Two growth factors were incorporated employing a multilayered coating based on polydopamine (PDA). In particular, Bone morphogenetic protein-2 (BMP-2) was bound onto the inner PDA layer while vascular endothelial growth factor (VEGF) was immobilized onto the outer one. Herein, the in vitro release of both growth factors is evaluated. A fastest VEGF delivery followed by a slow and more sustained release of BMP-2 was demonstrated, thus fitting the needs for bone tissue engineering applications. Due to the relevance of the crosstalk between bone-promoting and vessel-forming cells during bone healing, the functionalized scaffolds are further assessed on a co-culture setup of human mesenchymal stem cells and human endothelial progenitor cells. Osteogenic and angiogenic gene expression analysis indicates a synergistic effect between the growth factor-loaded scaffolds and the co-culture conditions. Taken together, these results indicate that the developed scaffolds hold great potential as an efficient platform for bone-tissue applications.

Indexed as

Neovascularization, PhysiologicOsteogenesisBone Morphogenetic Protein 2Cells, CulturedCoculture TechniquesEndothelial Progenitor CellsHumansIndolesMesenchymal Stem CellsPolymersTissue EngineeringTissue ScaffoldsVascular Endothelial Growth Factor ABMP2 protein, humanBone Morphogenetic Protein 2IndolespolydopaminePolymersVascular Endothelial Growth Factor AVEGFA protein, humanangiogenesisbone tissue engineeringco-deliverygrowth factorsmultilayersosteogenesispolydopaminescaffolds

Identifiers

PMID32899269
PMCPMC7503899
OpenAlexW3081808191

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.