Technology ID
TAB-3841

Method To Generate Chondrocytes from Human Induced Pluripotent Stem Cells (hIPSCs) and their use in Repairing Human Injury and Degenerative Diseases

E-Numbers
E-094-2023-0
Lead Inventor
Robey, Pamela (National Institute of Dental and Craniofacial Research (NIDCR))
Co-Inventors
Gadomski, Stephen
Applications
Therapeutics
Research Materials
Therapeutic Areas
Immunology
Development Stages
Discovery
Research Products
Human iPSC Lines
Human Cell Lines
Lead IC
NIDCR

This technology includes a method for differentiating human induced pluripotent stem cells (hiPSCs) into stable chondrocytes, capable of producing cartilage, and their use in cartilage repair in human injury and degenerative diseases. In suspension culture, hiPSC aggregates demonstrate gene and protein expression patterns similar to articular cartilage. Transplantation of cells from the aggregates into a mouse/rat femoral articular cartilage defect leads to the formation of stable, hyaline-like cartilage that persists for up to 5 months in immunocompromised mice and rats, demonstrating that hiPSC could potentially be used to regenerate cartilage in humans with similar defects. A potential application includes the treatment of osteoarthritis (OA), a disease characterized by the permanent loss of articular cartilage that lines joint surfaces.

Commercial Applications
In vivo long-term transplantation of hIPSC-derived chondrocytes can potentially be used to treat:
  • Injuries: This technology could be used to treat cartilage damage caused by injuries such as sports injuries, falls, and car accidents.
  • Overuse: This technology could be used to treat cartilage damage caused by overuse, such as in athletes and people who have physically demanding jobs.
  • Diseases: This technology could be used to treat cartilage damage caused by diseases such as osteoarthritis, rheumatoid arthritis, and avascular necrosis.
Competitive Advantages
This technology has the potential to be used to repair a variety of sources of cartilage damage, including damage caused by injury, overuse, and disease. In addition, the method described here produces chondrocytes that are stable when transplanted in vivo, which can potentially effect long-term and significant healing.
Licensing Contact:
Knezevic, Vladimir
vlado.knezevic@nih.gov