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DEVELOPMENT OF ANISOTROPY IN FIBROBLAST POPULATED COLLAGEN GELS

机译:成纤维胶原蛋白凝胶的各向异性发展

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The development of anisotropic mechanical properties is critical for the successful tissue engineering of many soft tissues. Load bearing tissues naturally develop varying degrees of anisotropy, presumably in response to their specific loading environment. For example, the heart wall develops a collagen structure that varies in a predictable manner through its depth. Tendon, on the other hand, develops a matrix that does not vary much in orientation and is highly aligned in the direction of muscle loading. These varied levels of anisotropy may be due to inherent differences between the cells in each tissue, to differences in the mechanical load and boundary conditions seen by the cells, or to a combination of these factors. The goal of this study is to understand the development of anisotropy in fibroblast populated collagen gels, with the ultimate goal of controlling this anisotropy for tissue engineering applications. In this study we set out to: 1) quantitatively determine the mechanical properties of gels in response to anisotropic external constraints, 2) determine whether this response is cell type specific, 3) determine whether the cells align with the direction of constraint, and 4) determine whether the collagen is realigned with the direction of constraint.
机译:各向异性力学性能的发展对于许多软组织的成功组织工程至关重要。承压组织自然会产生不同程度的各向异性,大概是响应于其特定的加载环境。例如,心脏壁形成胶原蛋白结构,该结构在其深度范围内以可预测的方式变化。另一方面,肌腱形成的基质的取向变化不大,并且在肌肉负荷的方向上高度对齐。这些不同水平的各向异性可能是由于每个组织中细胞之间的固有差异,由于细胞所见的机械负荷和边界条件的差异或这些因素的组合。这项研究的目的是了解成纤维细胞填充的胶原蛋白凝胶中各向异性的发展,其最终目的是为组织工程应用控制这种各向异性。在这项研究中,我们着手:1)定量确定响应于各向异性外部约束的凝胶的机械性能,2)确定该响应是否是特定于细胞类型的,3)确定细胞是否与约束方向对齐,以及4 )确定胶原蛋白是否与约束方向重新对齐。

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