Fan Hongbin, Hu Yunyu, Qin Ling, Li Xusheng, Wu Hong, Lv Rong
Institute of Orthopaedics and Traumatology, Xijing Hospital, The Fourth Military Medical University, Xi'an, People's Republic of China.
J Biomed Mater Res A. 2006 Jun 15;77(4):785-94. doi: 10.1002/jbm.a.30647.
The aim of the study was to produce a novel porous gelatin-chondroitin-hyaluronate scaffold in combination with a controlled release of transforming growth factor beta1 (TGF-beta1), which induced the differentiation of mesenchymal stem cells (MSCs) in vivo for enhancing cartilage repair. Gelatin microspheres loaded with TGF-beta1 (MS-TGFbeta1) showed a fast release at the initial phase (37.4%), and the ultimate accumulated release was 83.1% by day 18. The autologous MSCs seeded on MS-TGFbeta1/scaffold were implanted to repair full-thickness cartilage defects in rabbits as in vivo differentiation repair group, while MSCs differentiated in vitro were seeded on scaffold without MS-TGFbeta1 to repair the contra lateral cartilage defects (n = 30). Fifteen additional rabbits without treatment for defects were used as control. Histology observation showed that the in vivo differentiation repair group had better chondrocyte morphology, integration, continuous subchondral bone, and much thicker newly formed cartilage layer when compared to in vitro differentiation repair group 12 and 24 weeks, postoperatively. There was a significant difference in histological grading score between these two experimental groups, and both showed much better repair than that of the control. The present study implied that the novel scaffold with MS-TGFbeta1 might serve as a new way to induce the differentiation of MSCs in vivo to enhance the cartilage repair.
本研究的目的是制备一种新型的多孔明胶-软骨素-透明质酸支架,并结合转化生长因子β1(TGF-β1)的控释,以诱导间充质干细胞(MSCs)在体内分化,从而增强软骨修复。负载TGF-β1的明胶微球(MS-TGFβ1)在初始阶段显示出快速释放(37.4%),到第18天最终累积释放率为83.1%。将接种在MS-TGFβ1/支架上的自体间充质干细胞植入兔体内,修复全层软骨缺损,作为体内分化修复组,而将体外分化的间充质干细胞接种在不含MS-TGFβ1的支架上,修复对侧软骨缺损(n = 30)。另外15只未治疗缺损的兔作为对照。组织学观察表明,与体外分化修复组相比,体内分化修复组在术后12周和24周时软骨细胞形态、整合性、连续的软骨下骨以及新形成的软骨层更厚。这两个实验组的组织学分级评分存在显著差异,且两者均显示出比对照组更好的修复效果。本研究表明,含有MS-TGFβ1的新型支架可能是一种诱导间充质干细胞在体内分化以增强软骨修复的新方法。