Rowe Shaneen L, Lee Sungyun, Stegemann Jan P
Department of Biomedical Engineering, Rensselaer Polytechnic Institute, Troy, NY 12180-3590, USA.
Acta Biomater. 2007 Jan;3(1):59-67. doi: 10.1016/j.actbio.2006.08.006. Epub 2006 Nov 7.
Fibrin is a biopolymer that has been used in a variety of biomaterial, cell delivery and tissue engineering applications. The enzyme thrombin catalyzes the formation of fibrin microfibrils, which form a three-dimensional mesh in which cells can be directly embedded at the time of gel formation. In this study, fibrin hydrogels containing vascular smooth muscle cells were created using varying concentrations of thrombin. Over 7 days in culture, all gels decreased in volume as the fibrin matrix compacted, and the degree of gel compaction increased as thrombin concentration decreased. The material modulus and ultimate tensile stress of the gels also increased with decreasing thrombin concentration. Addition of thrombin to similar constructs made using collagen Type I did not show an effect on gel compaction or mechanical properties, suggesting that these effects were a result of thrombin's action on fibrin polymerization, and not cellular functions. Cell proliferation in fibrin hydrogels was not significantly affected by thrombin addition. Matrix examination using scanning electron microscopy showed increasing fibrin fiber diameters as thrombin concentration decreased. Confocal microscopic imaging of the actin cytoskeleton showed that cell morphology on two-dimensional substrates of fibrin showed marked changes, with higher thrombin concentrations producing cells with longer cellular projections. However, these morphological changes were not as apparent in cells embedded in three-dimensional (3-D) matrices, in which cells exhibited a similar morphology independent of thrombin concentration. These results relate features of the matrix and cellular components of 3-D fibrin constructs to mechanical properties, and contribute to the understanding of structure-function relationships in cell-seeded, 3-D protein hydrogels.
纤维蛋白是一种生物聚合物,已被用于多种生物材料、细胞递送和组织工程应用中。凝血酶催化纤维蛋白微纤维的形成,这些微纤维形成三维网状结构,细胞在凝胶形成时可直接包埋其中。在本研究中,使用不同浓度的凝血酶制备了含有血管平滑肌细胞的纤维蛋白水凝胶。在培养7天的过程中,随着纤维蛋白基质压实,所有凝胶体积均减小,且凝胶压实程度随凝血酶浓度降低而增加。凝胶的材料模量和极限拉伸应力也随凝血酶浓度降低而增加。向使用I型胶原制备的类似构建体中添加凝血酶对凝胶压实或力学性能没有影响,这表明这些影响是凝血酶对纤维蛋白聚合作用的结果,而非细胞功能的结果。在纤维蛋白水凝胶中添加凝血酶对细胞增殖没有显著影响。使用扫描电子显微镜进行的基质检查显示,随着凝血酶浓度降低,纤维蛋白纤维直径增大。对肌动蛋白细胞骨架进行共聚焦显微镜成像显示,在纤维蛋白二维基质上的细胞形态有明显变化,凝血酶浓度越高,细胞突起越长。然而,这些形态变化在包埋于三维(3-D)基质中的细胞中并不明显,在三维基质中,细胞呈现出与凝血酶浓度无关的相似形态。这些结果将三维纤维蛋白构建体的基质和细胞成分特征与力学性能联系起来,有助于理解细胞接种的三维蛋白质水凝胶中的结构-功能关系。