摘要
Background： Researchers initially proposed the substitution ofapoptotic chondrocytes in the superficial cartilage by injecting mesenchymal stem cells （MSCs） intraarticularly. This effect was termed as bio-resurfacing. Little evidence supporting the treatment ofosteoarthritis （OA） by the delivery ofa MSC suspension exists. The aim of this study was to investigate the effects of injecting allogenic MSCs intraarticularly in a rat OA model and to evaluate the influence of immobility on the effects of this treatment. Methods： We established a rat knee OA model after 4 and 6 weeks and cultured primary bone marrow MSCs. A MSC suspension was injected into the articular space once per week for 3 weeks. A subgroup of knee joints was immobilized for 3 days after each injection, while the remaining joints were nonimmobilized. We used toluidine blue staining, Mankin scores, and TdT-mediated dUTP-biotin nick end labeling staining to evaluate the therapeutic effect of the injections. Comparisons between the therapy side and the control side of the knee joint were made using paired t-test, and comparisons between the immobilized and nonimmobilized subgroups were made using the unpaired t-test. A P value 〈 0.05 was considered significant. Results： The three investigative approaches revealed less degeneration on the therapy sides of the knee joints than the control sides in both the 4- and 6-week groups （P 〈 0.05）, regardless of immobilization. No significant differences were observed between the immobilized and nonimmobilized subgroups （P 〉 0.05）. Conclusions： Therapy involving the intraarticular injection of allogenic MSCs promoted cartilage repair in a rat arthritis model, and 3-day immobility alter injection had little effect on this therapy.
Background： Researchers initially proposed the substitution ofapoptotic chondrocytes in the superficial cartilage by injecting mesenchymal stem cells （MSCs） intraarticularly. This effect was termed as bio-resurfacing. Little evidence supporting the treatment ofosteoarthritis （OA） by the delivery ofa MSC suspension exists. The aim of this study was to investigate the effects of injecting allogenic MSCs intraarticularly in a rat OA model and to evaluate the influence of immobility on the effects of this treatment. Methods： We established a rat knee OA model after 4 and 6 weeks and cultured primary bone marrow MSCs. A MSC suspension was injected into the articular space once per week for 3 weeks. A subgroup of knee joints was immobilized for 3 days after each injection, while the remaining joints were nonimmobilized. We used toluidine blue staining, Mankin scores, and TdT-mediated dUTP-biotin nick end labeling staining to evaluate the therapeutic effect of the injections. Comparisons between the therapy side and the control side of the knee joint were made using paired t-test, and comparisons between the immobilized and nonimmobilized subgroups were made using the unpaired t-test. A P value 〈 0.05 was considered significant. Results： The three investigative approaches revealed less degeneration on the therapy sides of the knee joints than the control sides in both the 4- and 6-week groups （P 〈 0.05）, regardless of immobilization. No significant differences were observed between the immobilized and nonimmobilized subgroups （P 〉 0.05）. Conclusions： Therapy involving the intraarticular injection of allogenic MSCs promoted cartilage repair in a rat arthritis model, and 3-day immobility alter injection had little effect on this therapy.
