OPTIMIZATION OF CRYOPRESERVATIVE PROCEDURES FOR HUMAN ARTICULAR-CARTILAGE CHONDROCYTES

Procedures are being developed which use isolated articular cartilage (AC) chondrocytes to restore damaged articular surfaces. The availability of isolated human chondrocytes for transplantation may be increased by low-temperature storage (banking). At present, no single method of freezing chondrocytes has been proven to be optimal. In this project, two different freezing protocols, I and II, were compared. Protocol I used freezing rates of -1-degree-C/min down to a temperature of -40-degrees-C. Protocol II used a freezing rate of -1-degree-C/min down to -10-degrees-C and faster rates thereafter. Cells were stored for 2 weeks at -196-degrees-C. Survival and function of the cells after thawing were evaluated by histological examination and determination of S-35 and H-3-thymidine incorporation after 1 and 2 weeks of high-density monolayer culture. Cells frozen with protocol I showed better function and survival (99.75%) than cells frozen with protocol II (85%). Both groups showed slowing of metabolism and replication after freezing when compared with controls. We conclude that controlled freezing of adult human chondrocytes at rates of -1-degree-C/min improves survival. Banking of human AC chondrocytes may be feasible using protocol I, although some questions regarding the long-term behaviour of human AC chondrocytes after cryopreservation remain to be answered.