创新性三维打印钛标本有利于在脂质体诱导矿化过程中调节牙髓干细胞的炎症。

Marialucia Gallorini, Alessia Ricci, Serena Pilato, Antonella Fontana, Carlo Mangano, Amelia Cataldi, Susi Zara
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引用次数: 0

摘要

目的:开发具有创新表面的定制钛试样是克服植入失败的合适策略。此外,更快、更有效的成骨承诺有助于组织再生。为了研究植入后炎症和分化之间的相互作用,牙髓干细胞(DPSCs)被培养在拥有内部开放细胞形式的 3D 打印钛上,与传统的分化培养基(DM)相比,该方法通过脂质体配方(LipoMix)施用成骨因子。材料和方法:成骨分化的评估方法包括:Western 印迹法测量 β1 整合素的表达;实时 RT-PCR 法测量 SP7 和胶原 I 基因的表达;血管生成的特征是测量血管内皮生长因子的分泌水平。基质矿化通过茜素红染色法进行评估,细胞粘附和炎症反应通过 Western 印迹法、酶法和 ELISA 法分别评估 Nrf2 表达、过氧化氢酶活性和前列腺素 E2 分泌:结果:LipoMix 可增强细胞增殖和粘附性,这体现在整合素 β1 表达的增加上。在 LipoMix 条件下,矿化基质沉积、SP7 基因表达、胶原 I 释放和碱性磷酸酶活性均有所增加。结论:所报告的数据证实,钛表面的内部形貌和后期制作处理可动态、积极地调节 DPSC 向成骨表型发展,此外,与 LipoMix 的结合可加快成骨条件下炎症的积极调节。因此,开发定制表面并在脂质体输送系统中施用分化因子,是牙科再生领域前景广阔的创新工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Innovative 3D-Printed Titanium Specimens Favor a Modulation of Inflammation in Dental Pulp Stem Cells During Liposome-Triggered Mineralization.

Purpose: developing customized titanium specimens, with innovative surfaces, is a suitable strategy to overcome implant failure. Additionally, a faster and efficient osteogenic commitment assists tissue regeneration. To investigate the interplay between inflammation and differentiation upon implantation, Dental Pulp Stem Cells (DPSCs) were cultured on 3D-printed titanium owning an internal open cell form, administering osteogenic factors by a liposomal formulation (LipoMix) compared to traditional delivery of differentiation medium (DM).

Materials and methods: osteogenic differentiation was evaluated by western blot, by measuring β1 integrin expression, and by and real-time RT-PCR, by measuring SP7 and Collagen I gene expression; while.angiogenesis was characterized by measuring VEGF secretion levels. Matrix mineralization was assessed by means of Alizarin Red Staining, cell adhesion and inflammation responses through western blot, enzymatic and ELISA assays evaluating Nrf2 expression, catalase activity and Prostaglandin E2 secretion, respectively.

Results: LipoMix enhances cell proliferation and adhesion, as revealed by increased integrin β1 expression. Mineralized matrix deposition, SP7 gene expression, Collagen I release and Alkaline Phosphatase activity appear increased in LipoMix condition. Additionally, the redox-sensitive transcription factor Nrf2 is overexpressed at the earliest experimental times, triggering the catalase activity.

Conclusions: data reported confirm that internal topography and post-production treatments on titanium surfaces dynamically and positively condition the DPSC progress towards the osteogenic phenotype, moreover, the combination with LipoMix fastens the positive modulation of inflammation under osteogenic conditions. Therefore, the development of customized surfaces along with the administration of differentiating factors enclosed in a liposomal delivery system, could represent a promising and innovative tool in regenerative dentistry.

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