Center for Stem Cell and Tissue Engineering, School of Medicine, Zhejiang University, Hangzhou, China.
Cell Transplant. 2009;18(10):1161-9. doi: 10.3727/096368909X12483162197169. Epub 2009 Aug 5.
Bone marrow released by microfracture or full-thickness cartilage defect can initiate the in situ cartilage repair. However, it can only repair small cartilage defects (<2 cm(2)). This study aimed to investigate whether autologous platelet-rich plasma (PRP) transplantation in collagen matrix can improve the in situ bone marrow-initiated cartilage repair. Full-thickness cartilage defects (diameter 4 mm, thickness 3 mm) in the patellar grooves of male New Zealand White rabbits were chosen as a model of in situ cartilage repair. They were treated with bilayer collagen scaffold (group II), PRP and bilayer collagen scaffold (group III), and untreated (group I), respectively (n = 11). The rabbits were sacrificed at 6 and 12 weeks after operation. The repaired tissues were processed for histology and for mechanical test. The results showed that at both 6 and 12 weeks, group III had the largest amounts of cartilage tissue, which restored a larger surface area of the cartilage defects. Moreover, group III had higher histological scores and more glycosaminoglycans (GAGs) content than those in the other two groups (p < 0.05). The Young's modulus of the repaired tissue in group II and group III was higher than that of group I (p < 0.05). Autologous PRP and bilayer collagen matrix stimulated the formation of cartilage tissues. The findings implicated that the combination of PRP with collagen matrix may repair larger cartilage defects that currently require complex autologous chondrocyte implantation (ACI) or osteochondral grafting.
微骨折或全层软骨缺损释放的骨髓可以启动原位软骨修复。然而,它只能修复小的软骨缺损(<2cm²)。本研究旨在探讨富血小板血浆(PRP)在胶原基质中的自体移植是否能改善原位骨髓启动的软骨修复。选用新西兰白兔髌骨关节沟内的全层软骨缺损(直径 4mm,厚度 3mm)作为原位软骨修复模型。分别采用双层胶原支架(II 组)、PRP 和双层胶原支架(III 组)和未处理(I 组)进行治疗(n = 11)。术后 6 和 12 周处死兔子。对修复组织进行组织学和力学测试。结果表明,在 6 周和 12 周时,III 组的软骨组织最多,可修复更大面积的软骨缺损。此外,III 组的组织学评分和糖胺聚糖(GAG)含量均高于其他两组(p < 0.05)。II 组和 III 组修复组织的杨氏模量高于 I 组(p < 0.05)。自体 PRP 和双层胶原基质刺激了软骨组织的形成。这些发现表明,PRP 与胶原基质的结合可能修复目前需要复杂的自体软骨细胞移植(ACI)或骨软骨移植的较大软骨缺损。