Lawrence Brian D, Pan Zhi, Weber Michael D, Kaplan David L, Rosenblatt Mark I
Margaret M. Dyson Vision Research Institute, Weill Cornell Medical College, USA.
J Vis Exp. 2012 Apr 24(62):3646. doi: 10.3791/3646.
Silk films are promising protein-based biomaterials that can be fabricated with high fidelity and economically within a research laboratory environment (1,2). These materials are desirable because they possess highly controllable dimensional and material characteristics, are biocompatible and promote cell adhesion, can be modified through topographic patterning or by chemically altering the surface, and can be used as a depot for biologically active molecules for drug delivery related applications (3-8). In addition, silk films are relatively straightforward to custom design, can be designed to dissolve within minutes or degrade over years in vitro or in vivo, and are produce with the added benefit of being transparent in nature and therefore highly suitable for imaging applications (9-13). The culture system methodology presented here represents a scalable approach for rapid assessments of cell-silk film surface interactions. Of particular interest is the use of surface patterned silk films to study differences in cell proliferation and responses of cells for alignment (12,14). The seeded cultures were cultured on both micro-patterned and flat silk film substrates, and then assessed through time-lapse phase-contrast imaging, scanning electron microscopy, and biochemical assessment of metabolic activity and nucleic acid content. In summary, the silk film in vitro culture system offers a customizable experimental setup suitable to the study of cell-surface interactions on a biomaterial substrate, which can then be optimized and then translated to in vivo models. Observations using the culture system presented here are currently being used to aid in applications ranging from basic cell interactions to medical device design, and thus are relevant to a broad range of biomedical fields.
丝素膜是一种很有前景的基于蛋白质的生物材料,在研究实验室环境中可以高保真且经济地制备(1,2)。这些材料之所以理想,是因为它们具有高度可控的尺寸和材料特性,具有生物相容性并能促进细胞黏附,可以通过形貌图案化或化学改变表面进行修饰,并且可以用作生物活性分子的储存库,用于与药物递送相关的应用(3 - 8)。此外,丝素膜相对容易进行定制设计,可以设计成在几分钟内溶解或在体外或体内数年降解,并且其制作还有一个额外的好处,即本质上是透明的,因此非常适合成像应用(9 - 13)。这里介绍的培养系统方法代表了一种可扩展的方法,用于快速评估细胞与丝素膜表面的相互作用。特别值得关注的是使用表面图案化的丝素膜来研究细胞增殖差异以及细胞排列反应(12,14)。将接种的培养物在微图案化和平坦的丝素膜基质上培养,然后通过延时相差成像、扫描电子显微镜以及代谢活性和核酸含量的生化评估进行分析。总之,丝素膜体外培养系统提供了一个可定制的实验装置,适用于研究生物材料基质上的细胞 - 表面相互作用,然后可以对其进行优化并转化为体内模型。使用这里介绍的培养系统所做的观察目前正被用于辅助从基本细胞相互作用到医疗设备设计等一系列应用,因此与广泛的生物医学领域相关。