Department of Bioengineering, University of Utah, United States; Scientific Computing and Imaging Institute, University of Utah, United States.
Department of Bioengineering, University of Utah, United States.
Acta Biomater. 2018 Jan;65:76-87. doi: 10.1016/j.actbio.2017.11.017. Epub 2017 Nov 8.
UNLABELLED: We developed a new method to manufacture dense, aligned, and porous collagen scaffolds using biaxial plastic compression of type I collagen gels. Using a novel compression apparatus that constricts like an iris diaphragm, low density collagen gels were compressed to yield a permanently densified, highly aligned collagen material. Micro-porosity scaffolds were created using hydrophilic elastomer porogens that can be selectively removed following biaxial compression, with porosity modulated by using different porogen concentrations. The resulting scaffolds exhibit collagen densities that are similar to native connective tissues (∼10% collagen by weight), pronounced collagen alignment across multiple length scales, and an interconnected network of pores, making them highly relevant for use in tissue culture, the study of physiologically relevant cell-matrix interactions, and tissue engineering applications. The scaffolds exhibited highly anisotropic material behavior, with the modulus of the scaffolds in the fiber direction over 100 times greater than the modulus in the transverse direction. Adipose-derived mesenchymal stem cells were seeded onto the biaxially compressed scaffolds with minimal cell death over seven days of culture, along with cell proliferation and migration into the pore spaces. This fabrication method provides new capabilities to manufacture structurally and mechanically relevant cytocompatible scaffolds that will enable more physiologically relevant cell culture studies. Further improvement of manufacturing techniques has the potential to produce engineered scaffolds for direct replacement of dense connective tissues such as meniscus and annulus fibrosus. STATEMENT OF SIGNIFICANCE: In vitro studies of cell-matrix interactions and the engineering of replacement materials for collagenous connective tissues require biocompatible scaffolds that replicate the high collagen density (15-25%/wt), aligned fibrillar organization, and anisotropic mechanical properties of native tissues. However, methods for creating scaffolds with these characteristics are currently lacking. We developed a new apparatus and method to create high density, aligned, and porous collagen scaffolds using a biaxial compression with porogens technique. These scaffolds have a highly directional structure and mechanical properties, with the tensile strength and modulus up to 100 times greater in the direction of alignment. We also demonstrated that the scaffolds are a suitable material for cell culture, promoting cell adhesion, viability, and an aligned cell morphology comparable to the cell morphology observed in native aligned tissues.
未加标签:我们开发了一种新方法,使用 I 型胶原凝胶的双向塑性压缩来制造致密、排列和多孔的胶原支架。使用一种新颖的压缩装置,该装置像虹膜一样收缩,将低密度胶原凝胶压缩以产生永久致密、高度排列的胶原材料。使用亲水性弹性体造孔剂制造微孔支架,这些造孔剂可以在双向压缩后选择性地去除,通过使用不同的造孔剂浓度来调节孔隙率。所得支架表现出与天然结缔组织相似的胶原密度(约 10%的胶原重量),在多个长度尺度上表现出明显的胶原排列,并且具有相互连接的孔网络,因此非常适合用于组织培养、研究生理相关的细胞-基质相互作用以及组织工程应用。支架表现出高度各向异性的材料行为,在纤维方向上的支架模量比横向方向上的模量高 100 多倍。脂肪来源的间充质干细胞在培养 7 天内接种到双向压缩的支架上,细胞死亡率很低,同时细胞增殖并迁移到孔腔中。这种制造方法提供了新的能力,可以制造结构和机械上相关的细胞相容支架,这将使更生理相关的细胞培养研究成为可能。进一步改进制造技术有可能生产用于直接替代半月板和纤维环等致密结缔组织的工程支架。
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