Center for System Integration Engineering, School of Integrated Design Engineering, Keio University, 3-1-14-1, Kohoku, Yokohama 223 0061, Japan.
Biomaterials. 2012 Mar;33(9):2693-700. doi: 10.1016/j.biomaterials.2011.12.039. Epub 2012 Jan 10.
There is great demand for constructing well-organized three-dimensional (3D) tissues in vitro. Here, we developed a 3D stacked culture method using biodegradable poly(d,l-lactide-co- glycolide) (PLGA) membranes with defined topography. Pore size and porosity of the membranes can be controlled by changing the moisture content during fabrication. The optimized membrane served as a scaffold to manipulate small hepatocyte (SH) layers when they were stacked, while it degraded after stacking, resulting in the reorganization of the cells into a 3D stacked structure. Immunofluorescent staining for domain markers of cell polarity and electron microscopy confirmed that the cells in the 3D stacked structures recovered polarity. Furthermore, the cells exhibited improved liver-specific function as compared with cells in a monolayer. This 3D stacked culture may enable reconstruction of multilayered hepatic tissues with highly differentiated functions in vitro.
体外构建组织有序的三维(3D)结构的需求很大。在这里,我们开发了一种使用具有明确定义的拓扑结构的可生物降解的聚(D,L-丙交酯-共-乙交酯)(PLGA)膜的 3D 堆叠培养方法。通过改变制造过程中的水分含量,可以控制膜的孔径和孔隙率。优化后的膜在堆叠时用作操纵小肝细胞(SH)层的支架,而在堆叠后降解,导致细胞重新组织成 3D 堆叠结构。细胞极性的域标记的免疫荧光染色和电子显微镜证实,3D 堆叠结构中的细胞恢复了极性。此外,与单层中的细胞相比,这些细胞表现出改善的肝特异性功能。这种 3D 堆叠培养方法可能使体外重建具有高度分化功能的多层肝组织成为可能。