Subramani K, Birch M A
Institute for Nanoscale Science and Technology, University of Newcastle upon Tyne, Newcastle upon Tyne, NE1 7AR, UK.
Biomed Mater. 2006 Sep;1(3):144-54. doi: 10.1088/1748-6041/1/3/009. Epub 2006 Jul 25.
The aims of this study were to fabricate poly(ethylene glycol) (PEG) hydrogel micropatterns on a biomaterial surface to guide osteoblast behaviour and to study how incorporating vascular endothelial growth factor (VEGF) within the adhered hydrogel influenced cell morphology. Standard photolithographic procedures or photopolymerization through a poly(dimethyl siloxane) (PDMS) mould were used to fabricate patterned PEG hydrogels on the surface of silanized silicon wafers. Hydrogel patterns were evaluated by light microscopy and surface profilometry. Rat osteoblasts were cultured on these surfaces and cell morphology investigated by fluorescence microscopy, scanning electron microscopy (SEM) and atomic force microscopy (AFM). Release of protein trapped in the polymerized PEG was evaluated and VEGF-PEG surfaces were characterized for their ability to support cell growth. These studies show that photopolymerized PEG can be used to create anti-adhesive structures on the surface of silicon that completely control where cell interaction with the substrate takes place. Using conventional lithography, structures down to 50 microm were routinely fabricated with the boundaries exhibiting sloping sides. Using the PDMS mould approach, structures were fabricated as small as 10 microm and boundaries were very sharp and vertical. Osteoblasts exhibiting typical morphology only grew on the silicon wafer surface that was not coated with PEG. Adding BSA to the monomer solution showed that protein could be released from the hydrogel for up to 7 days in vitro. Incorporating VEGF in the hydrogel produced micropatterns that dramatically altered osteoblast behaviour. At boundaries with the VEGF-PEG hydrogel, there was striking formation of cellular processes and membrane ruffling indicative of a change in cell morphology. This study has explored the morphogenetic properties of VEGF and the applications of nano/microfabrication techniques for guided tissue (bone) regeneration in dental and orthopaedic applications using osteoinductive PEG hydrogel micropatterns.
本研究的目的是在生物材料表面制备聚乙二醇(PEG)水凝胶微图案,以引导成骨细胞行为,并研究在粘附的水凝胶中加入血管内皮生长因子(VEGF)如何影响细胞形态。采用标准光刻工艺或通过聚二甲基硅氧烷(PDMS)模具进行光聚合,在硅烷化硅片表面制备图案化的PEG水凝胶。通过光学显微镜和表面轮廓仪对水凝胶图案进行评估。将大鼠成骨细胞培养在这些表面上,并通过荧光显微镜、扫描电子显微镜(SEM)和原子力显微镜(AFM)研究细胞形态。评估了被困在聚合PEG中的蛋白质释放情况,并对VEGF-PEG表面支持细胞生长的能力进行了表征。这些研究表明,光聚合PEG可用于在硅表面创建抗粘附结构,从而完全控制细胞与底物发生相互作用的位置。使用传统光刻技术,常规制备了尺寸小至50微米的结构,其边界呈现倾斜面。使用PDMS模具方法,制备的结构小至10微米,边界非常清晰且垂直。仅在未涂覆PEG的硅片表面上生长出具有典型形态的成骨细胞。向单体溶液中添加牛血清白蛋白(BSA)表明,蛋白质可在体外从水凝胶中释放长达7天。在水凝胶中加入VEGF产生的微图案显著改变了成骨细胞的行为。在与VEGF-PEG水凝胶的边界处,细胞突起和膜褶皱明显形成,表明细胞形态发生了变化。本研究探索了VEGF的形态发生特性,以及纳米/微加工技术在牙科和骨科应用中使用骨诱导性PEG水凝胶微图案进行引导组织(骨)再生的应用。