Kim E J, Kim N S, Lee G M
Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Taejon.
In Vitro Cell Dev Biol Anim. 1999 Apr;35(4):178-82. doi: 10.1007/s11626-999-0024-6.
To develop serum-free (SF) medium for dihydrofolate reductase-deficient Chinese hamster ovary cells (DG44), a statistical optimization approach based on a Plackett-Burman design was adopted. DG44 cells which were normally maintained in 10 serum medium were gradually weaned to 0.5% serum medium to increase the probability of successful growth in SF medium. A basal medium was prepared by supplementing Dulbecco's modified Eagle's medium and Ham's nutrient mixture F12 with hypoxanthine (10 mg/l) and thymidine (10 mg/l). Twenty-eight different supplements were selected as variables on the basis of their growth-promoting abilities. From statistical analysis, leucine, tryptophan, lysine, proline, histidine, hydrocortisone, ethanolamine, and phosphatidylcholine were identified as important components showing positive effects on cell growth. A new SF medium (SF-DG44) was formulated by supplementing the basal medium with these components. When the weaned cells were inoculated at 1.0 x 10(5) cells/ml, a maximum viable cell concentration of 6.4 x 10(3)) cells/ ml was achieved in SF-DG44 medium. In contrast, when the unweaned cells were used, a concentration of only 4.1 x 10(5) cells/ml was reached under the same culture conditions, indicating that weaning of cells improves cell growth in SF medium. In summary, we found that development of a novel SF medium for DG44 cells was facilitated using a Plackett-Burman design technique and weaning of cells.
为了开发用于二氢叶酸还原酶缺陷型中国仓鼠卵巢细胞(DG44)的无血清(SF)培养基,采用了基于Plackett-Burman设计的统计优化方法。通常在含10%血清的培养基中培养的DG44细胞逐渐过渡到含0.5%血清的培养基,以提高在无血清培养基中成功生长的概率。通过向杜氏改良 Eagle培养基和Ham's F12营养混合物中添加次黄嘌呤(10 mg/l)和胸腺嘧啶核苷(10 mg/l)来制备基础培养基。根据其促进生长的能力选择了28种不同的补充剂作为变量。通过统计分析,确定亮氨酸、色氨酸、赖氨酸、脯氨酸、组氨酸、氢化可的松、乙醇胺和磷脂酰胆碱是对细胞生长有积极影响的重要成分。通过向基础培养基中添加这些成分来配制一种新的无血清培养基(SF-DG44)。当将适应后的细胞以1.0×10⁵个细胞/ml接种时,在SF-DG44培养基中达到的最大活细胞浓度为6.4×10⁶个细胞/ml。相比之下,当使用未适应的细胞时,在相同培养条件下仅达到4.1×10⁵个细胞/ml的浓度,这表明细胞适应可改善其在无血清培养基中的生长。总之,我们发现使用Plackett-Burman设计技术和细胞适应有助于开发用于DG44细胞的新型无血清培养基。