Zheng J, Ito Y, Imanishi Y
Division of Material Chemistry, Faculty of Engineering, Kyoto University, Japan.
Biotechnol Prog. 1995 Nov-Dec;11(6):677-81. doi: 10.1021/bp00036a011.
An anchorage-dependent cell, mouse fibroblast STO cell and an anchorage-independent cell, K562 cell, were cultured on a polymer membrane coimmobilized with insulin and adhesion factors, poly(allylamine), and gelatin. The former is cationic and electrostatically (non-biospecifically) enhances cell adhesion, and the latter is a hydrolyzate of collagen and biospecifically enhances cell adhesion. They were immobilized onto a surface-hydrolyzed poly(methyl methacrylate) membrane by water-soluble carbodiimide. The adhesion of both STO and K562 cells was accelerated by the immobilization of poly(allylamine) or gelatin. The insulin immobilization did not affect adhesion of either cell. Although the growth of STO cells was enhanced on the insulin-immobilized membrane, the growth of K562 cells was not. However, the coimmobilizaiton of insulin and a cell-adhesion factor accelerated growth of both cells. It was considered that an increased frequency of interaction between the immobilized insulin and the receptor led to the cell growth acceleration.
将依赖贴壁的细胞(小鼠成纤维细胞STO细胞)和不依赖贴壁的细胞(K562细胞)培养在与胰岛素和黏附因子、聚烯丙胺及明胶共固定的聚合物膜上。前者呈阳离子性,通过静电作用(非生物特异性)增强细胞黏附,后者是胶原蛋白的水解产物,通过生物特异性增强细胞黏附。它们通过水溶性碳二亚胺固定在表面水解的聚甲基丙烯酸甲酯膜上。聚烯丙胺或明胶的固定加速了STO细胞和K562细胞的黏附。胰岛素的固定对两种细胞的黏附均无影响。虽然在固定有胰岛素的膜上STO细胞的生长得到增强,但K562细胞的生长并未增强。然而,胰岛素与细胞黏附因子的共固定加速了两种细胞的生长。据认为,固定化胰岛素与受体之间相互作用频率的增加导致了细胞生长加速。