Ninomiya N, Shirahata S, Murakami H, Sugahara T
Graduate School of Genetic Resources Technology, and Department of Food Science and Technology, Faculty of Agriculture, Kyushu University 46-09, 6-10-1 Hakozaki, Higashi-Ku, Fukuoka 812 Japan.
Biotechnol Bioeng. 1991 Nov;38(9):1110-3. doi: 10.1002/bit.260380920.
Large-scale, high-density freezing of hybridomas was studied to apply frozen cells to start high-density culture. We showed here that hybridomas can be frozen at 1.5 x 10(8) cells/mL, without decrement in viability and proliferating activity. Blood transporting bags were used for large-scale freezing to store 25 mL of cell suspension with a cell density, 1.5 x 10(8)/mL. The number of cells stored in a bag (3.0 x 10(9) cells) was enough to start a high-density culture at a 10 times higher cell density (6.0 x 10(6) cells/mL) than normal inoculation, and the cells proliferated to 10(7) cells/mL within 2 days. These results indicate that the large-scale freezing method is useful for large-scale culture of mammalian cells.
为了将冻存细胞用于启动高密度培养,对杂交瘤细胞进行了大规模、高密度冻存研究。我们在此表明,杂交瘤细胞可以1.5×10⁸个细胞/毫升的密度进行冻存,而活力和增殖活性不会降低。采用血液运输袋进行大规模冻存,以储存25毫升细胞密度为1.5×10⁸/毫升的细胞悬液。一个袋子中储存的细胞数量(3.0×10⁹个细胞)足以启动比正常接种细胞密度高10倍(6.0×10⁶个细胞/毫升)的高密度培养,且细胞在2天内增殖至10⁷个细胞/毫升。这些结果表明,大规模冻存方法对于哺乳动物细胞的大规模培养是有用的。