Department of Biomaterials, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Biomaterials. 2010 Apr;31(12):3307-16. doi: 10.1016/j.biomaterials.2010.01.034. Epub 2010 Feb 1.
To fight bone diseases characterized by poor bone quality like osteoporosis and osteoarthritis, as well as in reconstructive surgery, there is a need for a new generation of implantable biomaterials. It is envisioned that implant surfaces can be improved by mimicking the natural extracellular matrix of bone tissue, which is highly a organized nano-composite. In this study we aimed to get a better understanding of osteoblast response to nanometric grooved substrates varying in height, width and spacing. A throughput screening biochip was created using electron beam lithography. Subsequently, uniform large-scale nanogrooved substrates were created using laser interference lithography and reactive ion etching. Results showed that osteoblasts were responsive to nanopatterns down to 75 nm in width and 33nm in depth. SEM and TEM studies showed that an osteoblast-driven calcium phosphate (CaP) mineralization was observed to follow the surface pattern dimensions. Strikingly, aligned mineralization was found on even smaller nanopatterns of 50 nm in width and 17 nm in depth. A single cell based approach for real time PCR demonstrated that osteoblast-specific gene expression was increased on nanopatterns relative to a smooth control. The results indicate that nanogrooves can be a very promising tool to direct the bone response at the interface between an implant and the bone tissue.
为了对抗骨质疏松症和骨关节炎等骨骼质量差的骨骼疾病,以及进行重建手术,我们需要新一代的可植入生物材料。人们设想,可以通过模拟高度组织化的纳米复合材料的天然骨组织细胞外基质来改善植入物表面。在这项研究中,我们旨在更好地了解成骨细胞对高度、宽度和间距不同的纳米槽基底的反应。我们使用电子束光刻技术创建了高通量筛选生物芯片。随后,使用激光干涉光刻和反应离子刻蚀技术创建了均匀的大规模纳米槽基底。结果表明,成骨细胞对宽度为 75nm 且深度为 33nm 的纳米图案有反应。SEM 和 TEM 研究表明,观察到成骨细胞驱动的磷酸钙(CaP)矿化沿着表面图案的尺寸进行。引人注目的是,即使在宽度为 50nm 且深度为 17nm 的更小纳米图案上也发现了对齐的矿化。基于单细胞的实时 PCR 表明,与光滑对照相比,纳米图案上的成骨细胞特异性基因表达增加。结果表明,纳米凹槽可以成为一种非常有前途的工具,可用于指导植入物与骨组织之间界面的骨骼反应。