Basic Scientific Study
LAN Lingli, GU Wei, WANG Xuefeng, HAN Shangzhi, CHEN Xibo
Objective:To investigate the therapeutic effect of bone marrow mesenchymal stem cells (BMSCs) combined with platelet-rich fibrin (PRF) on temporomandibular joint osteoarthritis (TMJOA) in mice.
Methods:BMSCs isolated from C57BL/6J mice were evaluated for stem cell surface markers CD29, CD44, CD90, CD105, CD166 by flow cytometry. Osteogenic, adipogenic, and chondrogenic differentiation assays were performed to confirm the multilineage differentiation potential. A total of 120 8-week-old C57BL/6J mice were used to establish TMJOA models by bilateral disc removal. Approximately 0.1 mL of orbital blood was collected from each mouse to prepare PRF. Based on different treatments, joints were assigned to four groups: The control group (injection of 20 μL complete medium after disc removal), the BMSCs+PRF group (implantation of PRF combined with injection of 20 μL BMSCs suspension), the BMSCs group (injection of 20 μL BMSCs suspension only), and the PRF group (PRF implantation only). Mice were sacrificed in batches at 1, 2, 4 and 8 weeks postoperatively. The severity of the condylar cartilage degeneration was evaluated according to the modified Mankin scoring system after hematoxylin-eosin (HE) and Safranin O staining. Real-time quantitative polymerase chain reaction (RT-qPCR) was performed at 8 weeks postoperatively to assess the relative mRNA expression of Aggrecan, Sox9, Col1a1, Col2a1.
Results:Flow cytometric analysis and trilineage differentiation assays confirmed that the isolated cells exhibited typical characteristics of BMSCs. Histological assessment revealed the modified Mankin scores were significantly reduced in the BMSCs+PRF group compared with the control group, suggesting alleviated cartilage degeneration. Consistently, RT-qPCR analysis demonstrated a statistically significant increase in the mRNA levels of Aggrecan, Sox9, Col1a1, Col2a1 in the BMSCs+PRF group .
Conclusion:Combined application of BMSCs and PRF intra-articularly effectively alleviates TMJOA progression and promotes cartilage repair in mice.