Dental pulp stem cells in chitosan/gelatin scaffolds for enhanced orofacial bone regeneration

被引:69
作者
Bakopoulou, Athina [1 ]
Georgopoulou, Anthie [2 ]
Grivas, Ioannis [3 ]
Bekiari, Chryssa [3 ]
Prymak, Oleg [4 ,5 ]
Loza, Kateryna [4 ,5 ]
Epple, Matthias [4 ,5 ]
Papadopoulos, George C. [3 ]
Koidis, Petros [1 ]
Chatzinikolaidou, Maria [2 ,6 ]
机构
[1] Aristotle Univ Thessaloniki AUTh, Fac Hlth Sci, Sch Dent, Dept Prosthodont, Thessaloniki, Greece
[2] Univ Crete, Dept Mat Sci & Technol, Iraklion, Greece
[3] AUTh, Fac Hlth Sci, Sch Vet Med, Dept Anat Histol & Embryol, Thessaloniki, Greece
[4] Univ Duisburg Essen, Inorgan Chem, Duisburg, Germany
[5] Univ Duisburg Essen, Ctr Nanointegrat Duisburg Essen CeNIDE, Duisburg, Germany
[6] Fdn Res & Technol Hellas FORTH, IESL, Iraklion, Greece
关键词
Dental pulp stem cells; Bioinspired chitosan/gelatin scaffolds; Orofacial bone regeneration; MORPHOGENETIC PROTEIN-2; COMPOSITE SCAFFOLDS; BIOACTIVE GLASS; IN-VIVO; TISSUE; DIFFERENTIATION; CARTILAGE; RECONSTRUCTION; PROLIFERATION; FABRICATION;
D O I
10.1016/j.dental.2018.11.025
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Objective. Biomimetic chitosan/gelatin (CS/Gel) scaffolds have attracted great interest in tissue engineering of several tissues. However, limited information exists regarding the potential of combining CS/Gel scaffolds with oral cells, such as dental pulp stem cells (DPSCs), to produce customized constructs targeting alveolar/orofacial bone reconstruction, which has been the aim of the present study. Methods. Two scaffold types, designated as CS/Gel-0.1 and CS/Gel-1, were fabricated using 0.1 and 1% (v/v) respectively of the crosslinker glutaraldehyde (GTA). Scaffolds (n = 240) were seeded with DPSCs with/without pre-exposure to recombinant human BMP2. In vitro assessment included DPSCs characterization (flow cytometry), evaluation of viability/proliferation (live/dead staining, metabolic-based tests), osteo/odontogenic gene expression analysis (qRT-PCR) and structural/chemical characterization (scanning electron microscopy, SEM; energy dispersive X-ray spectroscopy, EDX; X-ray powder diffraction, XRD; thermogravimetry, TG). In vivo assessment included implantation of DPSC-seeded scaffolds in immunocompromised mice, followed by histology and SEM-EDX. Statistical analysis employed one/two-way ANOVA and Tukey's post-hoc tests (significance for p <0.05). Results. Both scaffolds supported cell viability/proliferation over 14 days in culture, showing extensive formation of a hydroxyapatite-rich nanocrystalline calcium phosphate phase. Differential expression patterns indicated GTA concentration to significantly affect the expression of osteo/odontogenic genes, with CS/Gel-0.1 scaffolds being more effective in upregulating DSPP, IBSP and Osterix. In vivo analysis demonstrated time-dependent production of a nanocrystalline, mineralized matrix at 6, 8 and 10 weeks, being more prominent in constructs bearing rhBMP-2 pre-treated cells. The latter showed higher amounts of osteoid and fully mineralized bone, as well as empty space reduction. Significance. These results reveal a promising strategy for orofacial bone tissue engineering. (C) 2018 The Academy of Dental Materials.
引用
收藏
页码:310 / 327
页数:18
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