Enhanced chondrogenic differentiation of iPS cell-derived mesenchymal stem/stromal cells via neural crest cell induction for hyaline cartilage repair

  • Front Cell Dev Biol. 2023 May 10:11:1140717. doi: 10.3389/fcell.2023.1140717.
Denise Zujur  1 Ziadoon Al-Akashi  1 Anna Nakamura  2 Chengzhu Zhao  1  3 Kazuma Takahashi  4 Shizuka Aritomi  4 William Theoputra  1 Daisuke Kamiya  1  5 Koichi Nakayama  2 Makoto Ikeya  1  5
Affiliations
  • 1. Center for iPS Cell Research and Application (CiRA), Kyoto University, Kyoto, Japan.
  • 2. Center for Regenerative Medicine Research, Faculty of Medicine, Saga University, Saga, Japan.
  • 3. Laboratory of Skeletal Development and Regeneration, Institute of Life Sciences, Chongqing Medical University, Chongqing, China.
  • 4. Research Institute for Bioscience Product and Fine Chemicals, Ajinomoto Co., Inc, Kawasaki, Japan.
  • 5. Takeda-CiRA Joint Program (T-CiRA), Kanagawa, Japan.
Abstract

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.

Keywords
cartilage; cell-based therapy; chondrocytes; chondrogenesis; induced mesenchymal stem/stromal cells; induced pluripotent stem cells; mesenchymal stem/stromal cells; tissue engineering.
Products