Department of Chemical Engineering, National Taiwan University, No. 1, Roosevelt Rd, Sec. 4, Taipei 106, Taiwan; Industrial Research Institute Swinburne (IRIS), and Department of Chemistry and Biotechnology, Faculty of Science, Engineering and Technology, Swinburne University of Technology, Hawthorn, 3122 VIC, Australia; CSIRO Materials Science and Engineering, Bayview Avenue, Clayton, 3168 VIC, Australia.
School of Chemical and Physical Sciences, Flinders University, Bedford Park, 5042 SA, Australia.
Acta Biomater. 2015 Jan;11:58-67. doi: 10.1016/j.actbio.2014.09.027. Epub 2014 Sep 22.
It is well known that the surface chemistry of biomaterials is important for both initial cell attachment and the downstream cell response. Surface chemistry gradients are a new format that allows the screening of the subtleties of cell-surface interactions in high throughput. In this study, two surface chemical gradients were fabricated using diffusion control during plasma polymerization via a tilted mask. Acrylic acid (AA) plasma polymer gradients were coated on a uniform 1,7-octadiene (OD) plasma polymer layer to generate OD-AA plasma polymer gradients, whilst diethylene glycol dimethyl ether (DG) plasma polymer gradients were coated on a uniform AA plasma polymer layer to generate AA-DG plasma polymer gradients. Gradient surfaces were characterized by X-ray photoelectron spectroscopy, infrared microscopy mapping, profilometry, water contact angle (WCA) goniometry and atomic force microscopy. Cell attachment density and differentiation into osteo- and adipo-lineages of rat-bone-marrow mesenchymal stem cells (rBMSCs) was studied on gradients. Cell adhesion after 24 h culture was sensitive to the chemical gradients, resulting in a cell density gradient along the substrate. The slope of the cell density gradient changed between 24 and 6 days due to cell migration and growth. Induction of rBMSCs into osteoblast- and adipocyte-like cells on the two plasma polymer gradients suggested that osteogenic differentiation was sensitive to local cell density, but adipogenic differentiation was not. Using mixed induction medium (50% osteogenic and 50% adipogenic medium), thick AA plasma polymer coating (>40 nm thickness with ∼11% COOH component and 35° WCA) robustly supported osteogenic differentiation as determined by colony formation and calcium deposition. This study establishes a simple but powerful approach to the formation of plasma polymer based gradients, and demonstrates that MSC behavior can be influenced by small changes in surface chemistry.
众所周知,生物材料的表面化学性质对于初始细胞附着和下游细胞反应都很重要。表面化学梯度是一种新的形式,它允许在高通量下筛选细胞表面相互作用的细微差别。在这项研究中,通过倾斜掩模在等离子体聚合过程中通过扩散控制来制造两种表面化学梯度。将丙烯酸(AA)等离子体聚合物梯度涂覆在均匀的 1,7-辛二烯(OD)等离子体聚合物层上,以生成 OD-AA 等离子体聚合物梯度,而将二甘醇二甲醚(DG)等离子体聚合物梯度涂覆在均匀的 AA 等离子体聚合物层上,以生成 AA-DG 等离子体聚合物梯度。通过 X 射线光电子能谱、红外显微镜映射、轮廓仪、水接触角(WCA)测角法和原子力显微镜对梯度表面进行了表征。研究了大鼠骨髓间充质干细胞(rBMSCs)在梯度表面上的附着密度和向成骨细胞和脂肪细胞谱系的分化。24 小时培养后细胞黏附对化学梯度敏感,导致细胞密度沿基底呈梯度分布。由于细胞迁移和生长,细胞密度梯度的斜率在 24 至 6 天之间发生变化。在两种等离子体聚合物梯度上诱导 rBMSCs 分化为成骨细胞样细胞和脂肪细胞样细胞表明,成骨细胞分化对局部细胞密度敏感,但脂肪细胞分化则不然。使用混合诱导培养基(50%成骨诱导培养基和 50%成脂诱导培养基),较厚的 AA 等离子体聚合物涂层(>40nm 厚度,具有约 11% COOH 成分和 35°WCA)通过集落形成和钙沉积强有力地支持成骨细胞分化。这项研究建立了一种简单但强大的制备等离子体聚合物梯度的方法,并表明 MSC 行为可以受到表面化学性质微小变化的影响。