Okuda A, Kajiwara Y, Kimura G
In Vitro. 1983 May;19(5):376-84. doi: 10.1007/BF02619554.
A semiserum-free medium was developed for monolayer culture of rat 3Y1 fibroblastic cells. The main components of the developed medium added to Dulbecco's modified Eagle's medium (DMEM) were insulin, transferrin, epidermal growth factor, poly-D-lysine, bovine albumin, oleic acid, and bovine alpha-globulin. In this medium, 3Y1 cells grew in mass culture at much the same rate as in DMEM supplemented with 10% fetal bovine serum (FBS), and colonies, albeit of smaller sizes, did form. Virally transformed derivatives of 3Y1 (simian virus 40-3Y1, polyoma virus-3Y1 and adenovirus type 12-3Y1) also formed colonies in the semiserum-free medium. When trypsinized 3Y1 cells were seeded with the medium lacking alpha-globulin, neither growth in the mass culture nor clonal growth in the low density culture (clonal growth) occurred. In this case, cell spreading was inhibited by albumin, and this inhibition was overcome by adding alpha-globulin or treating dishes with serum. When albumin was excluded from the semiserum-free medium, clonal growth did not occur, whereas growth in mass culture and stimulation of DNA synthesis in the resting mass culture (stimulation of DNA synthesis) were not so drastically affected. When oleic acid was removed, growth in mass culture was inhibited considerably, but no considerable effect was seen on clonal growth or on stimulation of DNA synthesis. In the absence of insulin, stimulation of DNA synthesis was inhibited more markedly than when other components were removed, but such was not the case with growth in mass culture and clonal growth.
开发了一种用于大鼠3Y1成纤维细胞单层培养的半无血清培养基。添加到杜尔贝科改良伊格尔培养基(DMEM)中的该培养基的主要成分有胰岛素、转铁蛋白、表皮生长因子、聚-D-赖氨酸、牛血清白蛋白、油酸和牛α球蛋白。在这种培养基中,3Y1细胞在大规模培养中的生长速度与在补充有10%胎牛血清(FBS)的DMEM中大致相同,并且确实形成了集落,尽管尺寸较小。3Y1的病毒转化衍生物(猿猴病毒40-3Y1、多瘤病毒-3Y1和12型腺病毒-3Y1)也在半无血清培养基中形成了集落。当用不含α球蛋白的培养基接种胰蛋白酶消化的3Y1细胞时,大规模培养中的生长和低密度培养中的克隆生长(克隆生长)均未发生。在这种情况下,白蛋白抑制细胞铺展,而添加α球蛋白或用血清处理培养皿可克服这种抑制作用。当从半无血清培养基中去除白蛋白时,克隆生长不会发生,而大规模培养中的生长和静止大规模培养中DNA合成的刺激(DNA合成的刺激)受到的影响没有那么大。当去除油酸时,大规模培养中的生长受到显著抑制,但对克隆生长或DNA合成的刺激没有明显影响。在没有胰岛素的情况下,DNA合成的刺激比去除其他成分时受到更明显的抑制,但大规模培养中的生长和克隆生长并非如此。