Arthritic diseases such as osteoarthritis (OA) and rheumatoid arthritis (RA) cause considerable pain, reduced mobility and significant disability among affected patients and present a major challenge to clinicians and basic scientists due to the limited inherent repair capacity of articular cartilage. The poor capacity of articular cartilage for self-repair is largely due to its avascular nature and has resulted in the development of a variety of surgical treatments including Autologous Chondrocyte Implantation (ACI) or Autologous Chondrocyte Transplantation (ACT), microfracture and mosaicplasty. Mesenchymal stem cells (MSCs) are multipotent progenitor cells with significant potential for chondrogenesis and new cartilage formation. Novel approaches using MSCs derived from bone marrow and adipose tissue have been proposed as alternatives to patient derived chondrocytes. In this paper we provide a scientific background to the biology of articular cartilage biology and its degeneration in arthritis. We also summarize some of the recent patents on applications of MSCs in articular cartilage tissue engineering and regenerative medicine for OA, RA and other joint diseases that involve cartilage degradation.
Osteoarthritis (OA), articular cartilage, mesenchymal stem cell, tissue engineering, regenerative medicine, patent, invention, rheumatoid arthritis, Autologous Chondrocyte Implantation, Autologous Chondrocyte Transplantation, microfracture, mosaicplasty, musculoskeletal, disorders, synovial joints, psoriatic arthritis, autoimmune diseases, subchondral bone, pathogenesis, extracellular matrix (ECM), Chondrocytes, proteoglycans, glycolytic cells, Hypoxia, normoxia, fibrilassociated collagens with interrupted helices (FACIT), decorin, biglycan, cartilage oligomeric matrix protein (COMP), physicochemical signals, osteophyte formation, obese juveniles, Pluripotent adult stem cells, hematopoietic stem cells, periosteum, trabecular bone, adipose tissue, synovium, density-gradient, centrifugation, nucleus pulposus (NP), biosynthesis, thrombin-like enzyme, venom, periodontal ligament, mineralization, thrombospondin, osteoblast, Cartilage-Bone Interface, tissue progenitor cells, biocompatible scaffold, hypoxiainducible factors (HIFs), organogenesis, reinfusion chamber, articular cartilage regeneration
Musculoskeletal Research Group, Division of Veterinary Medicine, School of Veterinary Medicine and Science, Faculty of Medicine and Health Sciences, University of Nottingham, Sutton Bonington Campus, Sutton Bonington, Leicestershire, LE12 5RD, UK.