International Center for Biotechnology, Osaka University, 2-1 Yamada-oka, Suita, Osaka, 565-0871, Japan.
Cytotechnology. 2005 Jan;47(1-3):11-7. doi: 10.1007/s10616-005-3751-x.
A differentiation method of human bone marrow mesenchymal stem cells (MSCs) to chondrocytes was developed for the construction of a three-dimensional (3D) cartilage tissue. The adhesive cells, which were isolated from a human bone marrow aspirate were embedded in type I collagen in a poly-L: -lactate-glycolic acid copolymer (PLGA) mesh and cultivated for 4 week together with growth factors. The degree of cellular differentiation was estimated by quantitative RT-PCR of aggrecan and type II collagen mRNAs and by staining with Safranin O. The 3D culture showed a higher degree of differentiation even without growth factors than the conventional pellet culture with growth factors, namely, dexamethasone and transforming growth factor (TGF)-beta 3. The 3D culture for 2 week with the combined addition of dexamethasone, TGF-beta 3, and insulin-like growth factor (IGF)-I reached a 30% expression of aggrecan mRNA compared with that in primary human chondrocytes, while the aggrecan mRNA expression in the conventional pellet culture was less than 2%. The sequential two-step differentiation cultivation, during which the cells were cultivated in 3D for 1 week after the conventional two-dimensional (2D) culture for 1 week, could markedly accelerate the expression of aggrecan mRNA compared with the 3D cultivation for 2 week.
建立三维(3D)软骨组织,开发了一种将人骨髓间充质干细胞(MSCs)分化为软骨细胞的方法。从骨髓抽吸物中分离出的黏附细胞嵌入 I 型胶原中,在聚 L: -乳酸-乙醇酸共聚物(PLGA)网中培养,并与生长因子一起培养 4 周。通过定量 RT-PCR 检测聚集蛋白聚糖和 II 型胶原 mRNA,并通过番红 O 染色来评估细胞分化程度。与具有生长因子(即地塞米松和转化生长因子(TGF)-β 3)的常规微球培养相比,即使没有生长因子,3D 培养也显示出更高的分化程度。在联合添加地塞米松、TGF-β 3 和胰岛素样生长因子(IGF)-I 的情况下,3D 培养 2 周可达到与原代人软骨细胞相比 30%的聚集蛋白聚糖 mRNA 表达,而常规微球培养中的聚集蛋白聚糖 mRNA 表达则不到 2%。在常规二维(2D)培养 1 周后进行为期 1 周的 3D 培养的两步序贯分化培养,可显著加速聚集蛋白聚糖 mRNA 的表达,而 3D 培养 2 周则可加速聚集蛋白聚糖 mRNA 的表达。