Department of Dental Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kamigyo-ku, Kyoto 602-8566, Japan.
Department of Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, 465 Kajii-cho, Kamigyo-ku, Kyoto 602-8566, Japan.
Int J Mol Sci. 2022 Jul 22;23(15):8099. doi: 10.3390/ijms23158099.
This study presents a set of vibrational characterizations on a nanogel-cross-linked porous freeze-dried gel (NanoCliP-FD gel) scaffold for tissue engineering and regenerative therapy. This scaffold is designed for the in vitro culture of high-quality cartilage tissue to be then transplanted in vivo to enable recovery from congenital malformations in the maxillofacial area or crippling jaw disease. The three-dimensional scaffold for in-plate culture is designed with interface chemistry capable of stimulating cartilage formation and maintaining its structure through counteracting the dedifferentiation of mesenchymal stem cells (MSCs) during the formation of cartilage tissue. The developed interface chemistry enabled high efficiency in both growth rate and tissue quality, thus satisfying the requirements of large volumes, high matrix quality, and superior mechanical properties needed in cartilage transplants. We characterized the cartilage tissue in vitro grown on a NanoCliP-FD gel scaffold by human periodontal ligament-derived stem cells (a type of MSC) with cartilage grown by the same cells and under the same conditions on a conventional (porous) atelocollagen scaffold. The cartilage tissues produced by the MSCs on different scaffolds were comparatively evaluated by immunohistochemical and spectroscopic analyses. Cartilage differentiation occurred at a higher rate when MSCs were cultured on the NanoCliP-FD gel scaffold compared to the atelocollagen scaffold, and produced a tissue richer in cartilage matrix. In situ spectroscopic analyses revealed the cell/scaffold interactive mechanisms by which the NanoCliP-FD gel scaffold stimulated such increased efficiency in cartilage matrix formation. In addition to demonstrating the high potential of human periodontal ligament-derived stem cell cultures on NanoCliP-FD gel scaffolds in regenerative cartilage therapy, the present study also highlights the novelty of Raman spectroscopy as a non-destructive method for the concurrent evaluation of matrix quality and cell metabolic response. In situ Raman analyses on living cells unveiled for the first time the underlying physiological mechanisms behind such improved chondrocyte performance.
本研究对纳米凝胶交联多孔冷冻干燥凝胶(NanoCliP-FD 凝胶)支架进行了一系列振动特性分析,该支架专为组织工程和再生治疗设计,用于体外培养高质量的软骨组织,然后移植到体内,以恢复面颌部的先天畸形或致残性颌骨疾病。用于板内培养的三维支架采用界面化学设计,能够通过对抗间充质干细胞(MSCs)在软骨组织形成过程中的去分化作用来刺激软骨形成并维持其结构。所开发的界面化学在生长速度和组织质量方面都具有高效率,从而满足了软骨移植所需的大体积、高基质质量和优异机械性能的要求。我们通过人牙周膜源性干细胞(一种 MSC)在 NanoCliP-FD 凝胶支架上体外培养的软骨组织,对其进行了特征描述,这些细胞与在传统(多孔)去端胶原支架上以相同条件培养的软骨组织进行了比较。通过免疫组织化学和光谱分析对不同支架上产生的软骨组织进行了比较评价。与去端胶原支架相比,MSC 在 NanoCliP-FD 凝胶支架上培养时,软骨分化速度更高,产生的软骨基质更丰富。原位光谱分析揭示了 NanoCliP-FD 凝胶支架刺激软骨基质形成效率提高的细胞/支架相互作用机制。本研究除了证明人牙周膜源性干细胞在 NanoCliP-FD 凝胶支架上再生软骨治疗中的高潜力外,还强调了拉曼光谱作为一种非破坏性方法同时评估基质质量和细胞代谢反应的新颖性。对活细胞的原位拉曼分析首次揭示了这种改善的软骨细胞性能背后的潜在生理机制。