Chrobak Kenneth M, Potter Daniel R, Tien Joe
Department of Biomedical Engineering, Boston University, MA 02215, USA.
Microvasc Res. 2006 May;71(3):185-96. doi: 10.1016/j.mvr.2006.02.005.
This work describes the formation, perfusion, and maturation of three-dimensional microvascular tubes in vitro. These tubes consisted of confluent monolayers of human endothelial cells that lined open, cylindrical channels within collagen gels. Perivascular cells could be directly embedded within the gels or added after endothelial cells grew to confluence. The tubes spanned the entire 5-7 mm extent of the gels; their diameters initially ranged from 55 to 120 microm and increased to 75-150 microm after maturation. Endothelial tubes displayed a strong barrier function over 5 days, resisted adhesion of leukocytes, and reacted quickly to inflammatory stimuli by breakdown of the barrier and support of leukocyte adhesion. These tubes resembled venules and "giant" capillaries in both their cellular organization and function, and we believe that they will serve as useful in vitro models of inflammation under constant perfusion.
这项工作描述了体外三维微血管管的形成、灌注和成熟过程。这些管子由人内皮细胞的汇合单层组成,它们排列在胶原凝胶内开放的圆柱形通道内。血管周细胞可以直接包埋在凝胶中,也可以在内皮细胞汇合后添加。这些管子跨越了凝胶的整个5 - 7毫米范围;它们的直径最初在55至120微米之间,成熟后增加到75 - 150微米。内皮管在5天内表现出强大的屏障功能,抵抗白细胞的黏附,并通过屏障的破坏和对白细胞黏附的支持对炎症刺激迅速做出反应。这些管子在细胞组织和功能上类似于微静脉和“巨型”毛细血管,我们相信它们将作为恒定灌注下炎症的有用体外模型。