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

被引:64
作者
Novais, Anita [1 ,2 ,3 ]
Lesieur, Julie [1 ,2 ]
Sadoine, Jeremy [1 ,2 ]
Slimani, Lotfi [1 ,2 ]
Baroukh, Brigitte [1 ,2 ]
Saubamea, Bruno [4 ]
Schmitt, Alain [5 ]
Vital, Sibylle [1 ,2 ,3 ]
Poliard, Anne [1 ,2 ]
Helary, Christophe [6 ]
Rochefort, Gael Y. [1 ,2 ]
Chaussain, Catherine [1 ,2 ,3 ]
Gorin, Caroline [1 ,2 ,3 ]
机构
[1] Univ Paris 05, Sorbonne Paris Cite, Dent Sch, EA Pathol Imagerie & Biotherapies Orofaciales 249, Montrouge, France
[2] Univ Paris 05, Sorbonne Paris Cite, Dent Sch, PIV, Montrouge, France
[3] Hop Univ PNVS, Charles Foix & Henri Mondor, AP HP, Dept Odontol, Ile De France, France
[4] Univ Paris 05, Sorbonne Paris Cite, Cellular & Mol Imaging Facil, Inserm US25,CNRS UMS 3612, Paris, France
[5] Univ Paris 05, Sorbonne Paris Cite, Cochin Inst,CNRS UMR8104, Transmiss Electron Microscopy Platform,INSERM U10, Paris, France
[6] Sorbonne Univ, Coll France, CNRS, Lab Chim Matiere Condensee Paris, Paris, France
关键词
Bone engineering; Mesenchymal stem cells; Hypoxia; Intramembranous ossification; Calvaria; SIDE POPULATION CELLS; IN-VITRO; COLLAGEN; REGENERATION; SCAFFOLD; MODEL; DIFFERENTIATION; VASCULARIZATION; RECONSTRUCTION; PROLIFERATION;
D O I
10.1002/sctm.18-0182
中图分类号
Q813 [细胞工程];
学科分类号
摘要
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.
引用
收藏
页码:844 / 857
页数:14
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