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首页> 外文期刊>Journal of Endodontics: Official Journal of American Association of Endodontists >Directional Migration and Odontogenic Differentiation of Bone Marrow Stem Cells Induced by Dentin Coated with Nanobioactive Glass
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Directional Migration and Odontogenic Differentiation of Bone Marrow Stem Cells Induced by Dentin Coated with Nanobioactive Glass

机译:用纳米硫酸盐涂覆牙本质骨髓干细胞的定向迁移和幼儿分化

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Introduction: This study aimed to use nanobioactive glass (nBG) to guide the directional migration of stem cells and odontogenic differentiation on primary dentin, which are important for the functional regeneration of pulp-dentin tissue. Methods: Human bone marrow stem cells (BMSCs) were cocultured with 0,5 mg/mL nBG. The cell-biomaterial interaction was monitored using the IncuCyte S3 live cell imaging system (Essen BioScience, Ann Arbor, MI). The adhesion and morphology of BMSCs growing on nBG-coated dentin were assessed at 2 hours and 3 days. The chemotaxis effect of nBG-coated dentin on BMSCs was tested using a 3-dimensional collagen gel model. Subcutaneous transplantation of nBG-treated dentin slices into nude mice was used to investigate cell homing and odontogenic differentiation in vivo. Results: nBG particles showed good biocompatibility, and they were gradually degraded and relocated during interactions with BMSCs. BMSCs had better initial attachment to an nBGcoated dentin surface than to an untreated dentin surface. Cell migration assays showed that nBG-coated dentin induced significantly more cell migration than untreated dentin. An in vivo study revealed that nBG-coated dentin slices facilitated recellularization and revascularization in the root canal and that dentin sialophosphoprotein-positive cells were detected on the surface of the primary dentin. Conclusions: nBG recruits stem cells to move toward dentin and further promotes cell adhesion and odontogenic differentiation on primary dentin, which help regenerate the biomimetic structure of pulp-dentin tissue.
机译:介绍:本研究旨在使用纳米氧活性玻璃(NBG)引导干细胞的定向迁移和原发性牙本质对原发性牙本质的牙道分化,这对于纸浆组织的功能再生是重要的。方法:将人骨髓干细胞(BMSCs)与0.5mg / ml NBG共培养。使用infucyte S3活细胞成像系统(Essen Bioscience,Ann Arbor,Mi)监测细胞 - 生物材料相互作用。在2小时和3天内评估在NBG涂覆的牙本质上生长的BMSC的粘附性和形态。使用三维胶原凝胶模型测试NBG涂覆的牙本质对BMSCs的趋化效应。将NBG处理的牙本质切片的皮下移植到裸鼠中,用于研究细胞归巢和体内牙育分化。结果:NBG颗粒显示出良好的生物相容性,它们在与BMSC的相互作用期间逐渐降解并重新定位。 BMSCs对Nbgcoated牙本质表面具有更好的初始附着,而不是未处理的牙本质表面。细胞迁移测定显示,NBG涂覆的牙本质诱导比未处理的牙本质更明显更多的细胞迁移。体内研究表明,NBG涂覆的牙本质切片促进了根管中的过度细胞和血运重建,并且在原发性牙本质的表面上检测到牙本质唾液酸磷蛋白阳性细胞。结论:NBG招募干细胞向牙本质移动,进一步促进原发性牙本质细胞粘附和异常分化,这有助于再生牙髓组织的仿真结构。

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