Technische Universität Dresden, Institute of Material Science, Chair for Biomaterials, Budapester Strasse 27, D-01069, Dresden, Germany.
Clinic for Operative and Pediatric Dentistry, Medical Faculty Carl Gustav Carus, TU Dresden, Fetscherstraße 74, D-01307, Dresden, Germany.
Head Face Med. 2017 Dec 8;13(1):23. doi: 10.1186/s13005-017-0156-y.
The revitalization or regeneration of the dental pulp is a preferable goal in current endodontic research. In this study, human dental pulp cell (DPC) spheres were applied to human root canal samples to evaluate their potential adoption for physiological tissue-like regeneration of the dental root canal by odontoblastic differentiation as well as cell-induced mineral formation.
DPC were cultivated into three-dimensional cell spheres and seeded on human root canal specimens. The evaluation of sphere formation, tissue-like behavior and differentiation as well as mineral formation of the cells was carried out with the aid of optical light microscopy, immunohistochemical staining and scanning electron microscopy (SEM).
Spheres and cells migrated out of the spheres showed an intense cell-cell- and cell-dentin-contact with the formation of extra cellular matrix. In addition, the ingrowth of cell processes into dentinal tubules and the interaction of cell processes with the tubule walls were detected by SEM-imaging. Immunohistochemical staining of the odontoblast specific matrix proteins, dentin matrix protein-1, and dentin sialoprotein revealed an odontoblast-like cell differentiation in contact with the dentin surface. This differentiation was confirmed by SEM-imaging of cells with an odontoblast specific phenotype and cell induced mineral formation.
The results of the present study reveal the high potential of pulp cells organized in spheres for dental tissue engineering. The odontoblast-like differentiation and the cell induced mineral formation display the possibility of a complete or partial "dentinal filling" of the root canal and the opportunity to combine this method with other current strategies.
牙髓的再生是当前牙髓学研究的一个理想目标。在本研究中,我们将牙髓细胞(DPC)球应用于人牙根样本,以评估其通过成牙本质细胞分化以及细胞诱导矿化来实现牙根生理性组织样再生的潜力。
将牙髓细胞培养成三维细胞球,并接种于人牙根尖样本上。借助光学显微镜、免疫组织化学染色和扫描电子显微镜(SEM),对球体形成、组织样行为和细胞分化以及矿化进行评估。
球体和从球体中迁移出来的细胞表现出强烈的细胞-细胞和细胞-牙本质接触,形成细胞外基质。此外,SEM 成像检测到细胞突起向牙本质小管内生长以及细胞突起与管壁的相互作用。牙本质基质蛋白 1 和牙本质涎磷蛋白的牙本质细胞特异性基质蛋白免疫组织化学染色显示,与牙本质表面接触的细胞具有成牙本质细胞样分化。SEM 成像显示具有成牙本质细胞特异性表型的细胞和细胞诱导的矿化进一步证实了这一点。
本研究结果揭示了球体组织的牙髓细胞在牙髓组织工程中的巨大潜力。成牙本质细胞样分化和细胞诱导矿化显示出完全或部分“牙本质填充”根管的可能性,并为将该方法与其他当前策略相结合提供了机会。