Department of Prosthodontics, School of Stomatology, Shandong University, Jinan, China.
Shandong Key Laboratory of Oral Tissue Regeneration & Shandong Engineering Laboratory for Dental Materials and Oral Tissue Regeneration, Jinan, China.
J Biomed Mater Res A. 2021 Aug;109(8):1429-1440. doi: 10.1002/jbm.a.37134. Epub 2020 Dec 11.
In order to explore the abilities of an integrated three-dimensional micro-nano topography in immunomodulation and promoting bone formation, present study focuses on the titanium sheets used in the micro-nano topography by treating them with the sandblasted, large-grit and acid-etched (SLA)and alkaline thermal reaction. Further, we characterized and obtained the surface morphology, roughness, and hydrophilicity of the titanium sheets. Moreover, we detected their in vitro cytocompatibility and cell proliferation as well. In addition, investigation was carried out for the immunomodulatory ability of the titanium sheets in a micro-nano topography by observing the expression of M1 (classical activated macrophage) and M2 (alternatively activated macrophage) type marker factors, inflammatory factors, and morphological changes of RAW264.7 cells cultured on the titanium sheets in different topographies. Through cell migration experiments and coculture, we observed the effects of different titanium sheet immune environments on osteoblast migration, extracellular matrix mineralization, and osteoblast gene expression. These results showed that the micro-nano topography constructed through SLA and alkaline thermal treatment improved the hydrophilicity and promoted the cell proliferation. Moreover, it promoted RAW264.7 cells to polarize as M2 phenotype, thereby leading to the anti-inflammatory effect of local microenvironments. This facilitated osteoblasts to secrete bone morphogenetic protein-2 (BMP2) and vascular endothelial growth factor. Nonetheless, these findings provided a theoretical basis for the molecular biological mechanism related to implants in a micro-nano topography which promoted the osteointegration while offering a meaningful theoretical basis for the clinical treatment of such implants.
为了探索整合三维微纳形貌在免疫调节和促进骨形成方面的能力,本研究集中在经过喷砂、大颗粒酸蚀(SLA)和碱性热反应处理的微纳形貌钛片上。进一步,我们对钛片的表面形貌、粗糙度和润湿性进行了表征和测定。此外,还检测了它们的体外细胞相容性和细胞增殖。此外,通过观察在不同形貌的钛片上培养的 RAW264.7 细胞中 M1(经典激活巨噬细胞)和 M2(替代激活巨噬细胞)型标记因子、炎症因子的表达以及形态变化,研究了微纳形貌钛片的免疫调节能力。通过细胞迁移实验和共培养,观察了不同钛片免疫环境对成骨细胞迁移、细胞外基质矿化和成骨细胞基因表达的影响。结果表明,通过 SLA 和碱性热处理构建的微纳形貌提高了亲水性并促进了细胞增殖。此外,它促进 RAW264.7 细胞向 M2 表型极化,从而导致局部微环境的抗炎作用。这促进了成骨细胞分泌骨形态发生蛋白 2(BMP2)和血管内皮生长因子。这些发现为促进骨整合的植入物相关分子生物学机制提供了理论依据,为植入物的临床治疗提供了有意义的理论基础。