Autologous chondrocyte transplantation.

The intrinsic capacity of cartilage to repair chondral injuries is poor. Different techniques to induce cartilage repair with the use of extrinsic chondrogeneic cell sources have been explored in experimental models. Cells can be harvested autologously or as allografts from a healthy part of the donor tissue, isolated, expanded in vitro, and finally implanted into the defect in high densities. Pure chondrocytes, epiphyseal or mature, allogeneic or autologous, and other types of mesenchymal cells have been used. The composition and structure of the extracellular cartilage matrix are maintained through a balance of anabolic and catabolic activities controlled by the unique chondrocytes. They keep the cartilage alive; they alone maintain it and regulate it. It therefore seems important to use true committed chondrocytes to repair a local cartilaginous defect. The rational basis for the use of committed autologous chondrocytes in combination with a covering periosteal membrane in the treatment of deep cartilage defects is presented.

[1]  C. Ohlsson,et al.  Rabbit Articular Cartilage Defects Treated With Autologous Cultured Chondrocytes , 1996, Clinical orthopaedics and related research.

[2]  C. Ohlsson,et al.  Treatment of deep cartilage defects in the knee with autologous chondrocyte transplantation. , 1994, The New England journal of medicine.

[3]  M. Brittberg,et al.  Influence of fibrin sealant (Tisseel) on osteochondral defect repair in the rabbit knee. , 1997, Biomaterials.

[4]  L. Peterson,et al.  The repair of experimentally produced defects in rabbit articular cartilage by autologous chondrocyte transplantation , 1989, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[5]  L. Culp,et al.  Fibronectin-mediated adhesion of fibroblasts: inhibition by dermatan sulfate proteoglycan and evidence for a cryptic glycosaminoglycan- binding domain , 1987, The Journal of cell biology.

[6]  K. Messner,et al.  Regional variations of indentation stiffness and thickness of normal rabbit knee articular cartilage. , 1996, Journal of biomedical materials research.

[7]  S W O'Driscoll,et al.  Role of oxygen tension during cartilage formation by periosteum , 1997, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[8]  E. Bell,et al.  Strategy for the selection of scaffolds for tissue engineering. , 1995, Tissue engineering.

[9]  R Langer,et al.  Joint resurfacing using allograft chondrocytes and synthetic biodegradable polymer scaffolds. , 1994, Journal of biomedical materials research.

[10]  R. Kandel,et al.  In vitro formation of mineralized cartilagenous tissue by articular chondrocytes , 1997, In Vitro Cellular & Developmental Biology - Animal.

[11]  V. Goldberg,et al.  Culture‐expanded human periosteal‐derived cells exhibit osteochondral potential in vivo , 1991, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

[12]  T. Aigner,et al.  Transplantation of allograft chondrocytes embedded in agarose gel into cartilage defects of rabbits. , 1998, Osteoarthritis and cartilage.

[13]  P. Benya,et al.  Dedifferentiated chondrocytes reexpress the differentiated collagen phenotype when cultured in agarose gels , 1982, Cell.

[14]  E B Hunziker,et al.  Articular cartilage repair: are the intrinsic biological constraints undermining this process insuperable? , 1999, Osteoarthritis and cartilage.