Mignot G, Dhainaut F, Diez Ibanez M, Chessebeuf-Padieu M, Padieu P
C R Seances Soc Biol Fil. 1986;180(4):460-72.
A rat liver epithelial cell line has been propagated on microcarriers in 11 or 21 laboratory culture vessels for cell culture in suspension on microcarriers (biogenerators) with Ham F10 or DME as basal synthetic culture medium either serum-supplemented (SSM), or serum-free (SFM), or serum- and protein-free (SPFM). Without serum, the use of DME allows a cellular growth in the biogenerator at least equivalent to that obtained in culture dishes. For the cultivation on microcarriers in SFM in a biogenerator the use during the first day of culture of spent serum-free medium previously incubated (SFMI) in confluent culture dishes avoids the substratum treatment with serum. Results concerning the Vero cell line cultured in SPFM are shown.
一种大鼠肝上皮细胞系已在11个或21个实验室培养容器中的微载体上进行传代培养,用于在以Ham F10或DME作为基础合成培养基的微载体(生物发生器)上进行悬浮细胞培养,培养基可为补充血清(SSM)、无血清(SFM)或无血清无蛋白(SPFM)。在无血清的情况下,使用DME可使生物发生器中的细胞生长至少等同于在培养皿中获得的生长情况。对于在生物发生器中于SFM中在微载体上进行培养,在培养的第一天使用先前在汇合培养皿中孵育过的无血清培养基(SFMI)可避免用血清处理基质。展示了在SPFM中培养的Vero细胞系的相关结果。