Chevrier A, Hoemann C D, Sun J, Buschmann M D
Chemical Engineering, Ecole Polytechnique, PO Box 6079, Station Centre-Ville, Montreal, Quebec, Canada.
Osteoarthritis Cartilage. 2007 Mar;15(3):316-27. doi: 10.1016/j.joca.2006.08.007. Epub 2006 Sep 26.
Marrow-stimulation techniques are used by surgeons to repair cartilage lesions although consistent regeneration of hyaline cartilage is rare. We have shown previously that autologous blood can be mixed with a polymer solution containing chitosan in a glycerol phosphate (GP) buffer (chitosan-GP), and that implantation of this polymer/blood composite onto marrow-stimulated chondral defects in rabbit and sheep leads to the synthesis of more chondral repair tissue with greater hyaline character compared to marrow-stimulation alone. In the current study, we examined the modulation of cell recruitment and repair tissue characteristics at early post-surgical time points (from day 1 to 56) in a rabbit model to elucidate potential mechanisms behind this improved repair outcome.
Thirty-three skeletally mature New Zealand White rabbits underwent bilateral arthrotomies, with each trochlea receiving a cartilage defect (3.5 mm x 4.5mm) bearing four microdrill holes (0.9 mm diameter, approximately 4 mm deep) into the subchondral bone. One defect per rabbit was treated with a chitosan-GP/blood implant, while the other defect was left as a microdrilled control. Repair tissues were stained by histochemistry, for collagen types I, II, and X by immunohistochemistry and analyzed using quantitative stereological tools.
Histological analyses demonstrated that control defects followed a typical healing sequence observed previously in marrow-stimulation animal models while chitosan-GP/blood implants led to three significant modifications in the healing sequence at early stages: (1) increased inflammatory and marrow-derived stromal cell recruitment to the microdrill holes, (2) increased vascularization of the provisional repair tissue in the microdrill holes, and (3) increased intramembranous bone formation and subchondral bone remodeling (BR).
These results suggest that the greater levels of provisional tissue vascularization and BR activity are main factors supporting improved cartilage repair when chitosan-GP/blood implants are applied to marrow-stimulated cartilage lesions.
外科医生采用骨髓刺激技术修复软骨损伤,然而透明软骨的持续再生却很罕见。我们之前已经表明,自体血可与含有壳聚糖的聚合物溶液在甘油磷酸(GP)缓冲液(壳聚糖 - GP)中混合,并且将这种聚合物/血液复合物植入兔和羊的骨髓刺激软骨缺损处,与单纯骨髓刺激相比,能产生更多具有更高透明软骨特征的软骨修复组织。在本研究中,我们在兔模型中研究了术后早期(第1天至56天)细胞募集和修复组织特征的调节情况,以阐明这种改善的修复结果背后的潜在机制。
33只骨骼成熟的新西兰白兔接受双侧关节切开术,每个滑车接受一个软骨缺损(3.5毫米×4.5毫米),在软骨下骨上有四个微钻孔(直径0.9毫米,约4毫米深)。每只兔子的一个缺损用壳聚糖 - GP/血液植入物治疗,另一个缺损作为微钻孔对照。修复组织通过组织化学染色,用免疫组织化学法检测I型、II型和X型胶原蛋白,并使用定量体视学工具进行分析。
组织学分析表明,对照缺损遵循先前在骨髓刺激动物模型中观察到的典型愈合顺序,而壳聚糖 - GP/血液植入物在早期愈合顺序中导致了三个显著变化:(1)炎症细胞和骨髓来源的基质细胞向微钻孔的募集增加;(2)微钻孔中临时修复组织的血管化增加;(3)膜内骨形成和软骨下骨重塑(BR)增加。
这些结果表明,当壳聚糖 - GP/血液植入物应用于骨髓刺激的软骨损伤时,临时组织血管化和BR活性的更高水平是支持软骨修复改善的主要因素。