Department of Removable Prosthodontics, School of Dentistry, Aichi Gakuin University, Nagoya, Japan.
J Prosthodont Res. 2021 Oct 15;65(4):474-481. doi: 10.2186/jpr.JPR_D_20_00114. Epub 2021 Feb 22.
Purpose Implants made of anodized-hydrothermally treated commercially pure titanium with a nanotopographic surface structure (SA-treated c.p.Ti) may advantageously promote contact osteogenesis during the early stages of healing. We hypothesized that utilizing SA-treated c.p.Ti with dental pulp stem cells (DPSCs) might improve osteoconduction during the process of osseointegration. This in vitro study investigated the effect of initial adhesion of DPSCs to SA-treated c.p.Ti compared with conventional c.p.Ti and anodic oxide (AO) c.p.Ti.Methods DPSCs were obtained from the mandibular incisors of Sprague-Dawley rats and cultured without osteogenic induction medium on c.p.Ti, AO c.p.Ti, and SA-treated c.p.Ti disks for up to 14 days. The morphology, proliferation, and differentiation of DPSCs were assessed by scanning electron microscopy, an MTT assay, and Alizarin Red S staining, respectively. A real-time quantitative polymerase chain reaction was used to quantify the mRNA expression of osteocalcin, osteopontin, and bone sialoprotein.Results On all disks, the DPSCs appeared flattened with the formation of extensions over time. The filopodium-like extensions were closely bound to the SA-treated c.p.Ti surface. The proliferation of DPSCs was not significantly different among the c.p.Ti treatments. However, DPSCs on SA-treated c.p.Ti showed the greatest mRNA levels of osteopontin, osteocalcin, and bone sialoprotein, as well as increased Alizarin Red S staining.Conclusions The results of the present in vitro study demonstrate that the surface properties of SA-treated c.p.Ti disks enhance osteogenic differentiation of DPSCs and may facilitate mineralized matrix formation on SA-treated c.p.Ti implant surfaces, which can enhance early bone regeneration.
具有纳米形貌表面结构的阳极氧化-水热处理商用纯钛(SA 处理 c.p.Ti)制成的植入物可能有利于在愈合的早期阶段促进接触成骨。我们假设利用 SA 处理 c.p.Ti 与牙髓干细胞(DPSCs)结合可能会提高在骨整合过程中的骨传导性。本体外研究调查了与传统 c.p.Ti 和阳极氧化(AO)c.p.Ti 相比,DPSCs 最初在 SA 处理 c.p.Ti 上黏附的效果。
从 Sprague-Dawley 大鼠的下颌切牙中获得 DPSCs,并在 c.p.Ti、AO c.p.Ti 和 SA 处理的 c.p.Ti 盘上培养,不使用成骨诱导培养基,培养时间长达 14 天。通过扫描电子显微镜、MTT 测定和茜素红 S 染色分别评估 DPSCs 的形态、增殖和分化。使用实时定量聚合酶链反应定量骨钙素、骨桥蛋白和骨唾液蛋白的 mRNA 表达。
在所有的盘上,随着时间的推移,DPSCs 呈现出扁平化,形成了延伸。丝状伪足样延伸与 SA 处理的 c.p.Ti 表面紧密结合。在 c.p.Ti 处理中,DPSCs 的增殖没有显著差异。然而,在 SA 处理的 c.p.Ti 上,DPSCs 的骨桥蛋白、骨钙素和骨唾液蛋白的 mRNA 水平最高,并且茜素红 S 染色增加。
本体外研究的结果表明,SA 处理 c.p.Ti 盘的表面特性增强了 DPSCs 的成骨分化,并可能促进 SA 处理 c.p.Ti 植入物表面矿化基质的形成,从而增强早期骨再生。