Priming Dental Pulp Stem Cells from Human Exfoliated Deciduous Teeth with Fibroblast Growth Factor-2 Enhances Mineralization Within Tissue-Engineered Constructs Implanted in Craniofacial Bone Defects

Author:

Novais Anita12,Lesieur Julie1,Sadoine Jérémy1,Slimani Lotfi1,Baroukh Brigitte1,Saubaméa Bruno3,Schmitt Alain4,Vital Sibylle12,Poliard Anne1,Hélary Christophe5,Rochefort Gaël Y.1,Chaussain Catherine12,Gorin Caroline12

Affiliation:

1. EA 2496 Pathologies, Imagerie et Biothérapies Orofaciales et Plateforme Imagerie du Vivant (PIV) Dental School, Université Paris Descartes Sorbonne Paris Cité, Montrouge, France

2. AP-HP Département d'Odontologie Hôpitaux Universitaires PNVS, Charles Foix et Henri Mondor, Ile de France, France

3. Cellular and Molecular Imaging Facility Inserm US25, CNRS UMS 3612, Faculté de Pharmacie de Paris, Université Paris Descartes Sorbonne Paris Cité, Paris, France

4. Cochin Institute, Transmission Electron Microscopy Platform, INSERM U1016, CNRS UMR8104 Université Paris Descartes Sorbonne Paris Cité, Paris, France

5. Laboratoire de Chimie de la Matière Condensée de Paris Sorbonne Universités, CNRS, Collège de France, Paris, France

Abstract

Abstract The craniofacial area is prone to trauma or pathologies often resulting in large bone damages. One potential treatment option is the grafting of a tissue-engineered construct seeded with adult mesenchymal stem cells (MSCs). The dental pulp appears as a relevant source of MSCs, as dental pulp stem cells display strong osteogenic properties and are efficient at bone formation and repair. Fibroblast growth factor-2 (FGF-2) and/or hypoxia primings were shown to boost the angiogenesis potential of dental pulp stem cells from human exfoliated deciduous teeth (SHED). Based on these findings, we hypothesized here that these primings would also improve bone formation in the context of craniofacial bone repair. We found that both hypoxic and FGF-2 primings enhanced SHED proliferation and osteogenic differentiation into plastically compressed collagen hydrogels, with a much stronger effect observed with the FGF-2 priming. After implantation in immunodeficient mice, the tissue-engineered constructs seeded with FGF-2 primed SHED mediated faster intramembranous bone formation into critical size calvarial defects than the other groups (no priming and hypoxia priming). The results of this study highlight the interest of FGF-2 priming in tissue engineering for craniofacial bone repair. Stem Cells Translational Medicine  2019;8:844–857

Funder

Fondation de la Recherche Médicale for Plateforme d'Imagerie du Vivant Paris Descartes

National French Agency

Fondation des Gueules Cassées

University Paris Descartes

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,General Medicine

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