1 Program of Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine , Stanford, California.
2 Department of Orthopedic Surgery, Stanford University School of Medicine , Stanford, California.
Tissue Eng Part A. 2018 Nov;24(21-22):1631-1640. doi: 10.1089/ten.TEA.2018.0011.
Hydrogels (HGs) are attractive matrices for cell-based cartilage tissue regeneration given their injectability and ability to fill defects with irregular shapes. However, most HGs developed to date often lack cell scale macroporosity, which restrains the encapsulated cells, leading to delayed new extracellular matrix deposition restricted to pericellular regions. Furthermore, tissue-engineered cartilage using conventional HGs generally suffers from poor mechanical property and fails to restore the load-bearing property of articular cartilage. The goal of this study was to evaluate the potential of macroporous gelatin-based microribbon (μRB) HGs as novel 3D matrices for accelerating chondrogenesis and new cartilage formation by human mesenchymal stem cells (MSCs) in 3D with improved mechanical properties. Unlike conventional HGs, these μRB HGs are inherently macroporous and exhibit cartilage-mimicking shock-absorbing mechanical property. After 21 days of culture, MSC-seeded μRB scaffolds exhibit a 20-fold increase in compressive modulus to 225 kPa, a range that is approaching the level of native cartilage. In contrast, HGs only resulted in a modest increase in compressive modulus of 65 kPa. Compared with conventional HGs, macroporous μRB scaffolds significantly increased the total amount of neocartilage produced by MSCs in 3D, with improved interconnectivity and mechanical strength. Altogether, these results validate gelatin-based μRBs as promising scaffolds for enhancing and accelerating MSC-based cartilage regeneration and may be used to enhance cartilage regeneration using other cell types as well.
水凝胶(HGs)由于其可注射性和能够填充具有不规则形状的缺陷的能力,是用于基于细胞的软骨组织再生的有吸引力的基质。然而,迄今为止开发的大多数 HG 通常缺乏细胞尺度的大孔,这限制了被包裹的细胞,导致新的细胞外基质的沉积延迟并且仅局限于细胞周围区域。此外,使用传统 HG 构建的组织工程软骨通常具有较差的机械性能,并且无法恢复关节软骨的承载性能。本研究的目的是评估大孔明胶基微带(μRB)HG 作为新型 3D 基质的潜力,以通过改善机械性能来加速人骨髓间充质干细胞(MSCs)在 3D 中的软骨生成和新软骨形成。与传统 HG 不同,这些 μRB HG 是固有大孔的,并且表现出类似于软骨的减震机械性能。在培养 21 天后,MSC 接种的 μRB 支架的压缩模量增加了 20 倍,达到 225 kPa,接近天然软骨的水平。相比之下,HG 仅导致压缩模量适度增加 65 kPa。与传统 HG 相比,大孔 μRB 支架显著增加了 MSC 在 3D 中产生的新软骨总量,并且具有改善的连通性和机械强度。总而言之,这些结果验证了基于明胶的 μRB 作为增强和加速 MSC 基于软骨再生的有前途的支架,并且可以用于增强使用其他细胞类型的软骨再生。