Hokkaido University, Kita-ku N13W8, Sapporo 060-8628, Japan.
J Biosci Bioeng. 2011 Apr;111(4):489-92. doi: 10.1016/j.jbiosc.2010.11.022. Epub 2010 Dec 24.
Aiming for the clinical application of cartilage regeneration, a culture method for mesenchymal stem cells (MSCs) derived from human bone marrow to obtain scaffold-free cartilage-like disk-shaped sheet of uniform sizes without the shrinkage was investigated. A disk-shaped cell sheet having the same diameter as that of the membrane without the shrinkage was formed after the cultivation of MSCs (18.6 × 10(5)cells/well) for 3 weeks in a cell culture insert (CCI) containing a flat membrane whose porosity was 12%, while 6.2 and 31.0 × 10(5)MSCs/well, respectively, resulted in the shrinkage of the aggregate and the hole formation in the center part of the sheet. Cell aggregates shrunk also in a 96-well plate and CCIs having lower porosity. The disk-shaped cell sheet showed the comparable thickness (1.2mm) and sulfated glycosaminoglycan (sGAG) density to those of the pellet formed in a pellet culture. The gene expression levels of aggrecan and type II collagen in the disk-shaped cell sheet were not lower than those in the pellet. In conclusion, the usage of CCI having 12% porosity and 18.6 × 10(5)MSCs/well could avoid the shrinkage from the formation of the scaffold-free cartilage-like disk-shaped cell sheet.
为了实现软骨再生的临床应用,研究了一种从人骨髓中提取间充质干细胞(MSCs)的培养方法,以获得无支架的、具有均匀大小的软骨样盘状细胞片,且不会收缩。在含有孔径为 12%的平膜的细胞培养插入物(CCI)中培养 MSCs(18.6×10(5)个/孔)3 周后,可形成与膜直径相同、无收缩的盘状细胞片,而分别培养 6.2×10(5)和 31.0×10(5)个 MSCs/孔,则会导致细胞聚集体收缩和细胞片中心部分出现孔。在 96 孔板和孔径较低的 CCI 中,细胞聚集体也会收缩。盘状细胞片的厚度(1.2mm)和硫酸化糖胺聚糖(sGAG)密度与在微球培养中形成的微球相当。盘状细胞片中聚集蛋白聚糖和 II 型胶原的基因表达水平不低于微球中的表达水平。综上所述,使用孔径为 12%、每孔接种 18.6×10(5)个 MSCs 的 CCI 可以避免无支架软骨样盘状细胞片的收缩。