Department of orthopaedics, Xijing Hospital, The Fourth Military Medical University, West Road Changle, Xi'an, China.
Joint Bone Spine. 2010 Jan;77(1):27-31. doi: 10.1016/j.jbspin.2009.05.013. Epub 2009 Dec 22.
This study was to evaluate the effect of hybrid microspheres (MS) composed of gelatin transforming growth factor-beta (TGF-beta1)-loaded MS and chitosan MS on the enhancement of differentiation of adipose-derived stem cells (ASCs) into chondrocytes in pellet culture in vitro and the reparative capacity of pellet from ASCs and the hybrid MS-TGF used to repair cartilage defects in vivo.
The morphology of the controlled-released MS was observed with scanning electron microscopy (SEM) and mechanical property was also tested in this study. In vitro TGF-beta1 release was evaluated by an enzyme-linked immunosorbent assay. The protein expression of Collagen II was tested by Western blot. In addition, a preliminary study on cartilage regeneration was also performed in vivo.
When chondrogenic differentiation of ASCs in both MS was evaluated, the protein expression of Collagen II became significantly increased for the hybrid MS-TGF, as compared with the gelatin MS-TGF. Mechanical result showed that the hybrid MS was superior to the gelatin MS. Observation of histology in vivo demonstrated that the pellet from ASCs and the hybrid MS-TGF promoted cartilage regeneration in the defects of articular cartilage much better than other groups.
Our study demonstrated that the pellet from ASCs and the hybrid MS-TGF can provide an easy and effective way to construct the tissue engineered cartilage in vitro and in vivo.
本研究旨在评估由载转化生长因子-β(TGF-β1)明胶微球(MS)和壳聚糖 MS 组成的杂交微球(MS)对体外微球培养中脂肪来源干细胞(ASCs)向软骨细胞分化的增强作用,以及 ASC 微球和用于体内修复软骨缺损的杂交 MS-TGF 的修复能力。
通过扫描电子显微镜(SEM)观察控释 MS 的形态,并对其力学性能进行测试。通过酶联免疫吸附试验(ELISA)评估 TGF-β1 的体外释放情况。通过 Western blot 检测 Collagen II 的蛋白表达。此外,还进行了体内软骨再生的初步研究。
在评估 MS 中 ASC 的软骨分化时,与明胶 MS-TGF 相比,杂交 MS-TGF 的 Collagen II 蛋白表达显著增加。力学结果表明,杂交 MS 优于明胶 MS。体内组织学观察表明,ASCs 微球和杂交 MS-TGF 比其他组更能促进关节软骨缺损处的软骨再生。
我们的研究表明,ASCs 微球和杂交 MS-TGF 可提供一种简便有效的方法,用于体外和体内构建组织工程化软骨。