Wu Chang-Chin, Sheu Shi-Yuan, Hsu Li-Ho, Yang Kai-Chiang, Tseng Chia-Chuan, Kuo Tzong-Fu
Department of Orthopedics, National Taiwan University Hospital, College of Medicine, National Taiwan University, Taipei, 10002, Taiwan.
Department of Orthopedics, En Chu Kong Hospital, New Taipei City, 23702, Taiwan.
J Biomed Mater Res B Appl Biomater. 2017 Aug;105(6):1536-1543. doi: 10.1002/jbm.b.33688. Epub 2016 Apr 29.
The use of mesenchymal stem cells (MSCs), which can be differentiated into chondrocytes under specific conditions, has been proposed for the treatment of cartilage defects. Blood-derived platelet-rich fibrin releasate (PRFr), which is rich in growth factors and cytokines, may improve cartilage regeneration. In this study, the therapeutic effects of PRFr in combination with bone marrow-derived MSCs for articular cartilage regeneration were evaluated in a rabbit model. Critical osteochondral defects were surgically created in the femoral condyle of the rabbits, and 3 × 10 of MSCs, 0.8 mL of PRFr, or a combination of MSCs and PRFr were injected intra-articularly and one week after first administration. The animals were sacrificed 12 weeks postoperatively, and the regenerated cartilages were assessed by gross inspection and histological examination. No treatment-related adverse events were noted in any of the rabbits. The size of the defect decreased and the volume of regenerated cartilage increased in the medial femoral condyles of the MSCs + PRFr group. Relative to the MSCs or PRFr group, histological examination demonstrated that the MSCs + PRFr group had thicker hyaline-like cartilaginous tissue with normal glycosaminoglycan production. Grading scores revealed that MSCs + PRFr injection had better matrix, cell distribution, and surface indices than other groups. The results showed that intra-articular injections of MSCs + PRFr into the knee can reduce cartilage defects by regenerating hyaline-like cartilage without adverse events. This approach may provide an alternative method of autologous chondrocyte implantation to repair cartilage defects with an unlimited source of cells and releasate. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 1536-1543, 2017.
间充质干细胞(MSCs)在特定条件下可分化为软骨细胞,已被提议用于治疗软骨缺损。富含生长因子和细胞因子的血液来源富血小板纤维蛋白释放物(PRFr)可能会促进软骨再生。在本研究中,在兔模型中评估了PRFr与骨髓来源的MSCs联合用于关节软骨再生的治疗效果。通过手术在兔股骨髁制造临界骨软骨缺损,将3×10个MSCs、0.8 mL PRFr或MSCs与PRFr的组合关节内注射,并在首次给药后一周再次注射。术后12周处死动物,通过大体检查和组织学检查评估再生软骨。所有兔子均未出现与治疗相关的不良事件。MSCs + PRFr组股骨内侧髁的缺损尺寸减小,再生软骨体积增加。组织学检查表明,相对于MSCs或PRFr组,MSCs + PRFr组具有更厚的透明样软骨组织,糖胺聚糖产生正常。分级评分显示,MSCs + PRFr注射组在基质、细胞分布和表面指标方面优于其他组。结果表明,向膝关节内注射MSCs + PRFr可通过再生透明样软骨减少软骨缺损,且无不良事件。这种方法可能为自体软骨细胞植入提供一种替代方法,以利用无限的细胞和释放物来源修复软骨缺损。© 2016威利期刊公司。《生物医学材料研究杂志》B部分:应用生物材料,105B:1536 - 1543,2017。