Objective: To examine the feasibility of autologous uncultured bone-marrow-derived mononuclear cells (BM-MNCs) in combination with microfracture in a full-thickness articular cartilage defect model so as to provide experimental rationales for clinical applications.
Methods: A total of 40 rabbits were divided randomly into groups A, B, C and D (n = 10 each). In groups A and C, 5 ml marrow samples were harvested from left femur and then autologous BM-MNCs isolated. The full-thickness articular cartilage defects were made on femoral intercondylar fossa in right knees of rabbits. Group A: micro-fracture was made on cartilage defect and then autologous uncultured BM-MNCs-autologous fibrin gel complex implanted; Group B:the same micro-fracture was made on cartilage defect and autologous fibrin gel implanted; Group C:the cartilage defect was implanted with autologous uncultured BM-MNCs-autologous fibrin gel complex; Group D:the cartilage defect was implanted with autologous fibrin gel. Five rabbits were sacrificed at Weeks 8 and 12 post-transplantation in each group. And the reparative tissue samples evaluated grossly, histologically and immunohistochemically were graded according to the gross and histological scales.
Results: The statistical analyses of histological gradings at Weeks 8 and 12 showed that group A was significantly better than groups B, C and D (P < 0.05), groups B and C were better than group D (P < 0.05) and each group at Week 12 was better than itself at Week 6 (P < 0.05).
Conclusion: Both of micro-fracture and transplantation of uncultured autologous BM-MNCs plus autologous fiber gel can promote the repair of cartilage defects. The combined use of micro-fracture and autologous uncultured BM-MNCs promotes the regeneration of articular cartilage so that it may provide theoretical rationales for clinical applications.