Bian Weining, Liau Brian, Badie Nima, Bursac Nenad
Department of Biomedical Engineering, Duke University, Durham, North Carolina, USA.
Nat Protoc. 2009;4(10):1522-34. doi: 10.1038/nprot.2009.155. Epub 2009 Sep 24.
This protocol describes a cell/hydrogel molding method for precise and reproducible biomimetic fabrication of three-dimensional (3D) muscle tissue architectures in vitro. Using a high aspect ratio soft lithography technique, we fabricate polydimethylsiloxane (PDMS) molds containing arrays of mesoscopic posts with defined size, elongation and spacing. On cell/hydrogel molding, these posts serve to enhance the diffusion of nutrients to cells by introducing elliptical pores in the cell-laden hydrogels and to guide local 3D cell alignment by governing the spatial pattern of mechanical tension. Instead of ultraviolet or chemical cross-linking, this method utilizes natural hydrogel polymerization and topographically constrained cell-mediated gel compaction to create the desired 3D tissue structures. We apply this method to fabricate several square centimeter large, few hundred micron-thick bioartificial muscle tissues composed of viable, dense, uniformly aligned and highly differentiated cardiac or skeletal muscle fibers. The protocol takes 4-5 d to fabricate PDMS molds followed by 2 weeks of cell culture.
本方案描述了一种细胞/水凝胶成型方法,用于在体外精确且可重复地仿生构建三维(3D)肌肉组织结构。利用高纵横比软光刻技术,我们制备了聚二甲基硅氧烷(PDMS)模具,其中包含具有特定尺寸、伸长率和间距的介观柱阵列。在细胞/水凝胶成型过程中,这些柱子通过在负载细胞的水凝胶中引入椭圆形孔隙来增强营养物质向细胞的扩散,并通过控制机械张力的空间模式来引导局部3D细胞排列。该方法不使用紫外线或化学交联,而是利用天然水凝胶聚合和地形约束的细胞介导凝胶压实来创建所需的3D组织结构。我们应用此方法制备了几平方厘米大、几百微米厚的生物人工肌肉组织,这些组织由有活力、致密、均匀排列且高度分化的心肌或骨骼肌纤维组成。制备PDMS模具需要4 - 5天,随后进行2周的细胞培养。