Watanabe K, Eto Y, Takano S, Nakamori S, Shibai H, Yamanaka S
Central Research Laboratories, Ajinomoto Co. Inc., Kawasaki, Japan.
Cytotechnology. 1993;13(2):107-14. doi: 10.1007/BF00749937.
A new substrate for mammalian cell culture was developed using a cellulose membrane produced by Acetobacter aceti. Modification of the ionic charge of the membrane and adsorption of collagen to it promoted cellular adhesion to the membrane surface. The growth of eight kinds of cells on the membrane, was comparable to that achieved in plastic Petri dishes. The membrane was tested for use in the production of recombinant Erythroid Differentiation Factor (EDF)/activin A using genetically engineered Chinese hamster ovary cells. Both the viability of the cells and production of EDF/activin A were maintained for about 1 month, while cultures on plastic dishes lasted only 12 days. It was considered that the mechanism of improved cell viability was related to the ultrastructure of the cellulose membrane.
利用醋酸杆菌生产的纤维素膜开发了一种用于哺乳动物细胞培养的新型基质。对膜的离子电荷进行修饰并使其吸附胶原蛋白,促进了细胞与膜表面的粘附。八种细胞在该膜上的生长情况与在塑料培养皿中的相当。使用基因工程改造的中国仓鼠卵巢细胞对该膜进行了生产重组红细胞分化因子(EDF)/激活素A的测试。细胞活力和EDF/激活素A的产量均维持了约1个月,而在塑料培养皿中的培养仅持续了12天。据认为,细胞活力提高的机制与纤维素膜的超微结构有关。