Central Research Laboratories, Ajinomoto Co., 1-1 Suzuki-chō, Kawasaki-ku, 210, Kawasaki, Japan.
Cytotechnology. 1991 Jan;5(Suppl 2):35-51. doi: 10.1007/BF00573879.
We tried to establish a new serum-free and heat-sterilizable medium, based on our serum-free medium in which many lymphoblastoid cells and hybridoma could grow as well as in a conventional serum-containing medium.As is well-known, L-glutamine (L-Gln) is one of the most heat-labile but essential components for cell growth. As a substitute for L-Gln, dipeptide such as Gly-L-Gln or L-Ala-L-Gln, which was quite stable even after autoclaving, was found to be utilizable for mammalian cell growth. The L-Gln dipeptide-containing serum-free medium was quite stable in a solution even after storing at 37°C for 4 months. In the serum-free medium containing L-Ala-L-Gln, mouse hybridola could grow and produce more antibody than in RPMI 1640+10% FBS.It has been proved that BSA and transferrin, which are also heat-labile but essential for the growth of various cell lines, can be substituted by heat-stable alpha-cyclodextrin and cholesterol, and Fe-gluconate, respectively. Insulin has also proved to be heat stable in a solution of Fe-gluconate. We thus established a new serum-free medium, all the components of which could be heat-sterilizable.Moreover, by adding EGF and BSA but without the adhesion factor included in FBS, the serum-free medium was found to support a long-term serial culture of a human diploid fibroblast.Finally, with this auotoclavable serum-free medium in a perfusion culture apparatus, we were able to continuously cultivate a human lymphoblastoid cell line. The production rate of IgM was found to be markedly increased by feeding the serum-free medium enriched by glucose, bicarbonate, L-Cys, and approtinin. The cell density reached as high as 2×10(8)/ml in the serum-free medium. Although the working volume in the reactor was only 1 1, the rate of IgM production reached 480 mg/day.The new heat-sterilizable serum-free medium has several advantages, because L-Gln peptide is a heat-stable and available precursor of L-Gln.
我们试图建立一种新的无血清和热灭菌培养基,这种培养基基于我们的无血清培养基,许多淋巴母细胞和杂交瘤细胞在其中能够生长,也可以在传统的含血清培养基中生长。众所周知,L-谷氨酰胺(L-Gln)是最不耐热但对细胞生长至关重要的成分之一。作为 L-Gln 的替代品,即使在高压灭菌后也非常稳定的二肽,如 Gly-L-Gln 或 L-Ala-L-Gln,可用于哺乳动物细胞生长。含有 L-Ala-L-Gln 的 L-Gln 二肽无血清培养基在溶液中即使在 37°C 下储存 4 个月也非常稳定。在含有 L-Ala-L-Gln 的无血清培养基中,鼠杂交瘤可以生长并产生比 RPMI 1640+10%FBS 更多的抗体。已经证明,BSA 和转铁蛋白也是各种细胞系生长所必需的,但不耐热,可以分别被热稳定的α-环糊精和胆固醇以及葡庚酸铁取代。胰岛素在葡庚酸铁溶液中也被证明是热稳定的。因此,我们建立了一种新的无血清培养基,其中所有成分都可以热灭菌。此外,通过添加 EGF 和 BSA,但不包含 FBS 中的粘附因子,发现无血清培养基支持人二倍体成纤维细胞的长期连续培养。最后,使用这种可热灭菌的无血清培养基在灌注培养装置中,我们能够连续培养人淋巴母细胞系。通过在无血清培养基中添加葡萄糖、碳酸氢盐、L-Cys 和 aprotinin 来丰富培养基,发现 IgM 的产量显著增加。细胞密度在无血清培养基中达到 2×10(8)/ml。尽管反应器中的工作体积仅为 1 升,但 IgM 的产量达到了 480mg/天。新的热灭菌无血清培养基具有几个优点,因为 L-Gln 肽是一种热稳定且可用的 L-Gln 前体。