Human treated dentin matrices combined with Zn-doped, Mg-based bioceramic scaffolds and human dental pulp stem cells towards targeted dentin regeneration

被引:33
作者
Bakopoulou, Athina [1 ]
Papachristou, Eleni [1 ]
Bousnaki, Maria [1 ]
Hadjichristou, Christina [1 ]
Kontonasaki, Eleana [1 ]
Theocharidou, Anna [1 ]
Papadopoulou, Lambrini [2 ]
Kantiranis, Nikolaos [2 ]
Zachariadis, George [3 ]
Leyhausen, Gabriele [4 ]
Geurtsen, Werner [4 ]
Koidis, Petros [1 ]
机构
[1] Aristotle Univ Thessaloniki, Sch Dent, Dept Fixed Prosthesis & Implant Prosthodont, GR-54124 Thessaloniki, Greece
[2] Aristotle Univ Thessaloniki, Fac Sci, Sch Geol, Dept Mineral Petr Ec Geol, GR-54124 Thessaloniki, Greece
[3] Aristotle Univ Thessaloniki, Dept Chem, Analyt Chem Lab, GR-54124 Thessaloniki, Greece
[4] Hannover Med Sch, Sch Dent, Dept Conservat Dent Periodontol & Prevent Dent, D-30625 Hannover, Germany
关键词
Mg-based; Zn-doped bioceramic scaffolds; Human Treated Dentin; Matrices-hTDMs; Dental Pulp Stem Cells-DPSCs; Dentin regeneration; GENE-EXPRESSION; IN-VIVO; TISSUE REGENERATION; CERAMIC SCAFFOLDS; FOLLICLE CELLS; PROTEIN-1; DMP1; BONE; DIFFERENTIATION; MAGNESIUM; RUNX2;
D O I
10.1016/j.dental.2016.05.013
中图分类号
R78 [口腔科学];
学科分类号
100302 [口腔临床医学];
摘要
Objective. This study aimed to investigate the potential of Mg-based bioceramic scaffolds combined with human treated-dentin matrices (hTDMs) and dentinogenesis-related morphogens to promote odontogenic differentiation and dentin-like tissue formation by Dental Pulp Stem Cells-DPSCs. Methods. DPSC cultures were established and characterized by flow cytometry. Experimental cavities were prepared inside crowns of extracted teeth and demineralized by EDTA (hTDMs). Zn-doped, Mg-based bioceramic scaffolds, synthesized by the sol gel technique, were hosted inside the hTDMs. DPSCs were spotted inside the hTDMs/scaffold constructs with/without additional exposure to DMP-1 or BMP-2 (100 ng/ml, 24h). Scanning Electron Microscopy-SEM, live/dead fluorescence staining and MTT assay were used to evaluate cell attachment and viability; Real time PCR for expression of osteo/odontogenic markers; Inductively Coupled Plasma-Atomic Emission Spectrometry-ICP/AES for scaffold elemental release analysis; ELISA for hTDM growth factor release analysis; SEM and X-ray Diffraction-XRD for structural/chemical characterization of the regenerated tissues. Results. Scaffolds constantly released low concentrations of Mg2+, Ca2+, Zn2+ and Si4+, while hTDMs growth factors, like DMP-1, BMP-2 and TGF beta-1. hTDMs/scaffold constructs supported DPSC viability, inducing their rapid odontogenic shift, indicated by upregulation of DSPP, BMP-2, osteocalcin and osterix expression. Newly-formed Ca-P tissue overspread the scaffolds partially transforming into bioapatite. Exposure to DMP-1 or BMP-2 pronouncedly enhanced odontogenic differentiation phenomena. Significance. This is the first study to validate that combining the bioactivity and ion releasing properties of bioceramic materials with growth factor release by treated natural dentin further supported by exogenous addition of key dentinogenesis-related morphogens (DMP-1, BMP-2) can be a promising strategy for targeted dentin regeneration. (C) 2016 The Academy of Dental Materials. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:E159 / E175
页数:17
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