Lowe Christopher J, Reucroft Ian M, Grota Matthew C, Shreiber David I
Department of Biomedical Engineering, Rutgers, The State University of New Jersey, 599 Taylor Road, Piscataway, New Jersey 08854, United States.
Department of Bioengineering, University of Massachusetts Dartmouth, 285 Old Westport Road, Dartmouth, Massachusetts 02747, United States.
ACS Biomater Sci Eng. 2016 Apr 11;2(4):643-651. doi: 10.1021/acsbiomaterials.6b00036. Epub 2016 Feb 25.
Matrix and cellular alignment are critical factors in the native function of many tissues, including muscle, nerve, and ligaments. Collagen is frequently a component of these aligned tissues, and collagen biomaterials are widely used in tissue engineering applications. However, the generation of aligned collagen scaffolds that maintain the native architecture of collagen fibrils has not been straightforward, with many methods requiring specialized equipment or technical procedures, extensive incubation times, or denaturing of the collagen. Herein, we present a simple, rapid method for fabrication of highly aligned collagen scaffolds. Collagen was assembled to form a fibrillar hydrogel in a cylindrical conduit with high aspect ratio and then frozen and lyophilized. The resulting collagen scaffolds demonstrated highly aligned topographical features along the scaffold surface. This presence of an initial fibrillar network and the high-aspect ratio vessel were both required to generate alignment. The diameter of fabricated scaffolds was found to vary significantly with both the collagen concentration of the hydrogel suspension and the diameter of conduits used for fabrication. Additionally, the size of individual aligned topographical features was significantly dependent on the conduit diameter and the freezing temperature. When cultured on aligned collagen scaffolds, both rat dermal fibroblasts and axons emerging from chick dorsal root ganglia explants demonstrated elongated, aligned morphology and growth on the aligned topographical features. Overall, this method presents a simple means for generating aligned collagen scaffolds that can be applied to a wide variety of tissue types, particularly those where such alignment is critical to native function.
基质和细胞排列是包括肌肉、神经和韧带在内的许多组织天然功能的关键因素。胶原蛋白通常是这些排列组织的组成部分,胶原蛋白生物材料广泛应用于组织工程领域。然而,生成能维持胶原纤维天然结构的排列型胶原蛋白支架并非易事,许多方法需要专门设备或技术程序、较长的孵育时间或使胶原蛋白变性。在此,我们提出一种简单、快速制备高度排列型胶原蛋白支架的方法。将胶原蛋白在高纵横比的圆柱形管道中组装形成纤维状水凝胶,然后冷冻并冻干。所得胶原蛋白支架在支架表面呈现出高度排列的形貌特征。生成排列需要初始纤维网络的存在和高纵横比的管道。发现制备的支架直径随水凝胶悬浮液的胶原蛋白浓度和用于制备的管道直径显著变化。此外,单个排列的形貌特征大小显著取决于管道直径和冷冻温度。当在排列型胶原蛋白支架上培养时,大鼠真皮成纤维细胞和从鸡背根神经节外植体长出的轴突均在排列的形貌特征上呈现出伸长、排列的形态并生长。总体而言,该方法提供了一种生成排列型胶原蛋白支架的简单手段,可应用于多种组织类型,特别是那些这种排列对天然功能至关重要的组织类型。