Department of Sports Medicine and Joint Surgery, Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
J Biomed Mater Res A. 2012 Sep;100(9):2244-51. doi: 10.1002/jbm.a.34165. Epub 2012 Apr 10.
The purpose of this study was to determine the in vivo cartilage induction effect of the poly(2-acrylamido-2-methylpropanesulfonic acid) (PAMPS) single-network (SN) gel and poly(N,N'-dimethyl acrylamide) (PDMAAm) SN gel in comparison with that of the PAMPS/PDMAAm double-network (DN) gel. An osteochondral defect created in rabbit trochlea was treated with PAMPS/PDMAAm DN, PAMPS SN, or PDMAAm SN gel implantation or left untreated. The gel was implanted into the defect so that a 2-mm depth remained. The defects were examined by histologic and immunohistochemical evaluations, surface assessment using confocal laser scanning microscopy, and real-time polymerase chain reaction analysis at 4 weeks. Samples were quantitatively evaluated with a scoring system reported by Wayne et al. The PAMPS/PDMAAm DN gel-implanted defect was filled with the hyaline-like cartilage tissue. The PAMPS SN gel-implanted defect was filled inhomogenously with hyaline/fibrocartilage tissue. The histology score of the defect treated with PAMPS/PDMAAm DN gel was significantly higher than those treated with PAMPS and PDMAAm SN gels, and the untreated defect (p = 0.0408, p < 0.0001, and p < 0.0001, respectively) and the scores of the defect treated with PAMPS SN gel were significantly higher than those treated with PDMAAm SN gel and the untreated defect (p = 0.0026 and p = 0.0026, respectively). These results suggested that the PAMPS SN gel has an ability that can induce hyaline cartilage regeneration in vivo, but that the PDMAAm SN gel does not. The current study indicates that the chondrogenic potential of a negatively charged PAMPS gel component plays an important role in the cartilage regeneration ability of the PAMPS/PDMAAm DN gel in vivo.
本研究旨在比较聚(2-丙烯酰胺基-2-甲基丙磺酸)(PAMPS)单网络(SN)凝胶和聚(N,N'-二甲基丙烯酰胺)(PDMAAm)SN 凝胶与 PAMPS/PDMAAm 双网络(DN)凝胶的体内软骨诱导效果。在兔滑车的骨软骨缺损中,用 PAMPS/PDMAAm DN、PAMPS SN 或 PDMAAm SN 凝胶植入物或不进行治疗来处理凝胶。将凝胶植入缺陷中,使深度保持在 2 毫米。在 4 周时通过组织学和免疫组织化学评估、使用共聚焦激光扫描显微镜进行表面评估以及实时聚合酶链反应分析来检查缺陷。使用 Wayne 等人报道的评分系统对样本进行定量评估。PAMPS/PDMAAm DN 凝胶植入的缺陷充满了透明样软骨组织。PAMPS SN 凝胶植入的缺陷不均匀地填充有透明/纤维软骨组织。用 PAMPS/PDMAAm DN 凝胶处理的缺陷的组织学评分明显高于用 PAMPS 和 PDMAAm SN 凝胶处理的缺陷,并且未处理的缺陷(p = 0.0408、p < 0.0001 和 p < 0.0001)和用 PAMPS SN 凝胶处理的缺陷评分明显高于用 PDMAAm SN 凝胶和未处理的缺陷(p = 0.0026 和 p = 0.0026)。这些结果表明,PAMPS SN 凝胶具有在体内诱导透明软骨再生的能力,但 PDMAAm SN 凝胶没有。本研究表明,带负电荷的 PAMPS 凝胶成分的软骨形成潜力在 PAMPS/PDMAAm DN 凝胶在体内的软骨再生能力中发挥重要作用。