Department of Biomedical Engineering, Johns Hopkins School of Medicine, Baltimore, Maryland, USA.
Tissue Eng Part A. 2010 Jul;16(7):2255-63. doi: 10.1089/ten.TEA.2009.0584.
We present a novel approach to control endothelial tubulogenesis by spatially patterning cells within micromolded collagen gels. Endothelial cells cultured within microscale channels that were filled with collagen gel organized into tubes with lumens within 24-48 h of seeding. These tubes extended up to 1 cm in length, and exhibited cell-cell junction formation characteristic of early stage capillary vessels. Tube diameter could be controlled by varying collagen concentrations or channel width. The geometry of the microfabricated template also could be used to guide the development of branches during tube formation, allowing for the generation of more complex capillary architectures. Time-lapse imaging of tube formation revealed a highly dynamic process involving coalescence of endothelial cells, reorganization and alignment of collagen fibers into a central core, and arrangement of cells into cords. This platform may be of use to generate geometrically defined vascular networks for tissue engineering applications as well as a means to better understand the process of endothelial tubulogenesis.
我们提出了一种新的方法,通过在微成型胶原凝胶中对细胞进行空间图案化来控制内皮细胞小管的生成。在微通道中培养的内皮细胞,在接种后 24-48 小时内填充胶原凝胶,形成具有管腔的管。这些管延伸长达 1 厘米,并且表现出具有早期毛细血管特征的细胞-细胞连接形成。通过改变胶原浓度或通道宽度可以控制管的直径。微加工模板的几何形状也可用于在管形成过程中引导分支的发育,从而产生更复杂的毛细血管结构。管形成的延时成像显示了一个高度动态的过程,涉及内皮细胞的融合、胶原纤维的重新组织和排列成中央核心,以及细胞排列成索。该平台可用于生成用于组织工程应用的几何定义的血管网络,也可用于更好地理解内皮小管生成的过程。