软骨发生
间充质干细胞
细胞生物学
软骨
干细胞
再生医学
透明软骨
诱导多能干细胞
细胞外基质
间质细胞
细胞分化
化学
生物
解剖
病理
胚胎干细胞
癌症研究
医学
骨关节炎
关节软骨
生物化学
替代医学
基因
作者
Denise Zujur,Ziadoon Al-Akashi,Anna Nakamura,Chengzhu Zhao,Kazuma Takahashi,Shizuka Aritomi,William Theoputra,Daisuke KAMIYA,Koichi Nakayama,Makoto Ikeya
标识
DOI:10.3389/fcell.2023.1140717
摘要
Background: To date, there is no effective long-lasting treatment for cartilage tissue repair. Primary chondrocytes and mesenchymal stem/stromal cells are the most commonly used cell sources in regenerative medicine. However, both cell types have limitations, such as dedifferentiation, donor morbidity, and limited expansion. Here, we report a stepwise differentiation method to generate matrix-rich cartilage spheroids from induced pluripotent stem cell-derived mesenchymal stem/stromal cells (iMSCs) via the induction of neural crest cells under xeno-free conditions. Methods: The genes and signaling pathways regulating the chondrogenic susceptibility of iMSCs generated under different conditions were studied. Enhanced chondrogenic differentiation was achieved using a combination of growth factors and small-molecule inducers. Results: We demonstrated that the use of a thienoindazole derivative, TD-198946, synergistically improves chondrogenesis in iMSCs. The proposed strategy produced controlled-size spheroids and increased cartilage extracellular matrix production with no signs of dedifferentiation, fibrotic cartilage formation, or hypertrophy in vivo . Conclusion: These findings provide a novel cell source for stem cell-based cartilage repair. Furthermore, since chondrogenic spheroids have the potential to fuse within a few days, they can be used as building blocks for biofabrication of larger cartilage tissues using technologies such as the Kenzan Bioprinting method.
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