Division of Drug Delivery and Tissue Engineering, Centre for Biomolecular Sciences, School of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Biofabrication. 2014 Sep;6(3):035003. doi: 10.1088/1758-5082/6/3/035003. Epub 2014 Apr 11.
Electrospinning is a common technique used to fabricate fibrous scaffolds for tissue engineering applications. There is now growing interest in assessing the ability of collector plate design to influence the patterning of the fibres during the electrospinning process. In this study, we investigate a novel method to generate hybrid electrospun scaffolds consisting of both random fibres and a defined three-dimensional (3D) micro-topography at the surface, using patterned resin formers produced by rapid prototyping (RP). Poly(D,L-lactide-co-glycolide) was electrospun onto the engineered RP surfaces and the ability of these formers to influence microfibre patterning in the resulting scaffolds visualized by scanning electron microscopy. Electrospun scaffolds with patterns mirroring the microstructures of the formers were successfully fabricated. The effect of the resulting fibre patterns and 3D geometries on mammalian cell adhesion and proliferation was investigated by seeding enhanced green fluorescent protein labelled 3T3 fibroblasts onto the scaffolds. Following 24 h and four days of culture, the seeded scaffolds were visually assessed by confocal macro- and microscopy. The patterning of the fibres guided initial cell adhesion to the scaffold with subsequent proliferation over the geometry resulting in the cells being held in a 3D micro-topography. Such patterning could be designed to replicate a specific in vivo structure; we use the dermal papillae as an exemplar here. In conclusion, a novel, versatile and scalable method to produce hybrid electrospun scaffolds has been developed. The 3D directional cues of the patterned fibres have been shown to influence cell behaviour and could be used to culture cells within a similar 3D micro-topography as experienced in vivo.
静电纺丝是一种常用于制造组织工程应用纤维支架的常见技术。现在人们越来越感兴趣的是评估收集器板设计在静电纺丝过程中影响纤维图案形成的能力。在这项研究中,我们研究了一种新方法,使用快速原型制作(RP)生产的图案化树脂成型器,生成由随机纤维和表面上定义的三维(3D)微形貌组成的混合静电纺丝支架。聚(D,L-丙交酯-共-乙交酯)被静电纺到工程化的 RP 表面上,并通过扫描电子显微镜观察这些成型器对所得支架中微纤维图案形成的影响。成功制造了与成型器微结构镜像的静电纺丝支架。通过将增强型绿色荧光蛋白标记的 3T3 成纤维细胞接种到支架上来研究所得纤维图案和 3D 几何形状对哺乳动物细胞黏附和增殖的影响。培养 24 小时和 4 天后,通过共聚焦宏观和显微镜对接种的支架进行视觉评估。纤维的图案化引导细胞初始黏附到支架上,随后在几何形状上增殖,从而使细胞保持在 3D 微形貌中。这种图案化可以设计为复制特定的体内结构;我们在这里以真皮乳头为例。总之,已经开发出一种新颖、多功能且可扩展的生产混合静电纺丝支架的方法。图案化纤维的 3D 定向线索已被证明会影响细胞行为,并可用于在类似于体内经历的 3D 微形貌中培养细胞。