Repair of cartilage defects in osteoarthritis rats with induced pluripotent stem cell derived chondrocytes

BMC Biotechnol. 2016 Nov 9;16(1):78. doi: 10.1186/s12896-016-0306-5.

Abstract

Background: The incapacity of articular cartilage (AC) for self-repair after damage ultimately leads to the development of osteoarthritis. Stem cell-based therapy has been proposed for the treatment of osteoarthritis (OA) and induced pluripotent stem cells (iPSCs) are becoming a promising stem cell source.

Results: Three steps were developed to differentiate human iPSCs into chondrocytes which were transplanted into rat OA models induced by monosodium iodoacetate (MIA). After 6 days embryonic body (EB) formation and 2 weeks differentiation, the gene and protein expression of Col2A1, GAG and Sox9 has significantly increased compare to undifferentiated hiPSCs. After 15 weeks transplantation, no immune responses were observed, micro-CT showed gradual engraftment and the improvement of subchondrol plate integrity, and histological examinations demonstrated articular cartilage matrix production.

Conclusions: hiPSC could be an efficient and clinically translatable approach for cartilage tissue regeneration in OA cartilages.

Keywords: Chondrocyte; Differentiation; Osteoarthritis; Transplantation; iPSC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cartilage, Articular / growth & development*
  • Cartilage, Articular / immunology
  • Cartilage, Articular / pathology
  • Cell Differentiation / immunology
  • Cells, Cultured
  • Chondrocytes / cytology*
  • Chondrocytes / immunology
  • Chondrocytes / transplantation*
  • Chondrogenesis / immunology
  • Induced Pluripotent Stem Cells / cytology*
  • Osteoarthritis / immunology
  • Osteoarthritis / pathology*
  • Osteoarthritis / therapy*
  • Rats
  • Rats, Sprague-Dawley
  • Treatment Outcome