Department of Biomedical Engineering, School of Engineering and School of Medicine, National Taiwan University, Taipei, Taiwan.
Tissue Eng Part A. 2020 Jan;26(1-2):102-110. doi: 10.1089/ten.TEA.2019.0142. Epub 2019 Sep 20.
Electrospun materials are widely used for functional tissue engineering for its robust production and biomimetic properties. Several issues persist, however, including heterogeneous cell distribution, insufficient matrix elaboration/accumulation, and limited construct size. We took three synergistic approaches to address these issues by modifying the chemical microenvironment for the seeded cells. Instead of the commonly used fibronectin, we demonstrated that type I collagen (COL) coating, facilitated by polydopamine treatment, promoted cell infiltration into the fibrous scaffold and resulted in homogeneous distribution in one week. Sequential treatment with fibroblast growth factor and transforming growth factor-β after cell infiltration enhanced cell proliferation and matrix deposition, with increased lysyl oxidase and decreased matrix metalloproteinase-1 expressions. Finally, lamination of the fibrous sheets with fibrin gel not only increased construct size, but further stimulated COL deposition and improved construct mechanical functionalities in combination with sequential growth factor supplementation. These soluble and insoluble chemical optimizations encouraged rapid and robust construct development for a functional engineered ligament graft and can be adapted for the engineering of other tissues. Impact Statement Ligament and tendon injuries are some of the most common orthopedic injuries with long-term repercussions. Tissue engineered grafts provide a promising alternative to autograft and allografts. We present in this study robust and synergistic chemical optimization approaches for the functional engineering of ligament grafts. Moreover, these approaches can be adapted for a variety of other tissues to improve homogeneous construct development.
静电纺丝材料因其强大的生产能力和仿生特性而被广泛用于功能性组织工程。然而,仍存在一些问题,包括细胞分布不均匀、基质积累不足和构建体尺寸有限。我们通过改变接种细胞的化学微环境,采取了三种协同方法来解决这些问题。我们证明,与常用的纤维连接蛋白相比,通过聚多巴胺处理促进的 I 型胶原(COL)涂层有利于细胞渗透到纤维支架中,并在一周内实现均匀分布。细胞渗透后,用成纤维细胞生长因子和转化生长因子-β进行序贯处理,可促进细胞增殖和基质沉积,同时增加赖氨酰氧化酶的表达,降低基质金属蛋白酶-1 的表达。最后,将纤维片与纤维蛋白凝胶层压不仅增加了构建体的尺寸,而且通过结合序贯生长因子补充进一步刺激 COL 沉积和改善构建体的机械功能。这些可溶性和不溶性化学优化方法促进了功能性工程韧带移植物的快速和稳健构建,并可适应其他组织的工程。
影响陈述
韧带和肌腱损伤是最常见的骨科损伤之一,会产生长期影响。组织工程移植物为自体移植物和同种异体移植物提供了有前途的替代方案。我们在这项研究中提出了用于功能性工程韧带移植物的强大且协同的化学优化方法。此外,这些方法可以适应多种其他组织,以改善均匀的构建体发展。