Department of Molecular Pharmacology, Physiology, and Biotechnology, Center for Biomedical Engineering, Brown University, Providence, Rhode Island 02912, USA.
Tissue Eng Part A. 2010 Jun;16(6):2051-61. doi: 10.1089/ten.TEA.2009.0607.
A significant challenge of tissue engineering is to build tissues whose size is not limited by diffusion. We are investigating the use of scaffold-free lumen containing toroid-shaped microtissues as minimal building units. Monodispersed H35 cells, a rat hepatocyte cell line, were seeded onto micromolded agarose, forming self-assembled multicellular toroids within 48 h. Toroid and lumen diameter were easily controlled by micromold design, and toroid thickness was controlled by seeding density. When harvested, toroids were stable, but underwent predictable changes over time with their lumens narrowing. When brought into contact, these building units fused in the x-y plane, forming a double-lumen structure, as well as the z plane, forming a tubular structure, which completed within 72 h. Large, multi-luminal structures were assembled by multidimensional fusion of many toroids. Toroid settling was not entirely random, with most toroids lying flat with their lumens oriented along the z axis. The rapid production of toroid building units of controlled dimension and lumen size that undergo predictable changes and that can be fused to form larger structures is a step closer to tissue engineering large porous three-dimensional tissues with high cell density.
组织工程的一个重大挑战是构建不受扩散限制的组织。我们正在研究使用无支架腔包含环形微组织作为最小构建单元。将单分散 H35 细胞,一种大鼠肝细胞系,接种到微成型琼脂糖上,在 48 小时内形成自组装的多细胞环形物。环形物和腔的直径可以通过微模具设计轻松控制,而环形物的厚度可以通过接种密度控制。收获时,环形物稳定,但随着时间的推移,其腔会变窄,发生可预测的变化。当这些构建单元接触时,它们在 x-y 平面上融合,形成双腔结构,以及 z 平面,形成管状结构,这在 72 小时内完成。通过许多环形物的多维融合来组装大型多腔结构。环形物的沉降并不是完全随机的,大多数环形物是平的,其腔沿着 z 轴定向。快速生产具有可预测变化且可融合形成更大结构的受控尺寸和腔尺寸的环形物构建单元,是朝着使用高细胞密度的大孔三维组织工程组织更近了一步。