Shapiro L E, Wagner N
Department of Medicine, Montefiore Medical Center, Bronx, New York.
In Vitro Cell Dev Biol. 1988 Apr;24(4):299-303. doi: 10.1007/BF02628831.
Serum-free tissue culture medium consisting of a 1:1 mixture of Dulbecco's modified Eagle's medium (DMEM) and Ham's F12 medium is herein shown to support growth of Reuber H-35 cells over several days in culture. Cells were initially plated in serum containing DMEM medium for 3 h. After cell attachment, serum is removed and replaced with a serum-free 1:1 mixture of these two commercially available tissue culture media. The doubling time of cell growth in this unsupplemented serum-free medium was 46 h in lightly plated cultures over the first 5 d. The presence of transferrin (5 micrograms/ml) and insulin (3.3 nM) results in a cell doubling time of 17 h, which equaled the growth rate in medium containing 10% fetal bovine serum. In the absence of transferrin, growth rates in serum-free medium were correlated with the cell density of cultures. Conditioned medium from dense, serum-free cultures has growth-stimulating activity in recipient lightly plated cultures. This simple, serum-free culture medium will facilitate studies on the growth regulation of H-35 rat hepatoma cells.
由杜尔贝科改良伊格尔培养基(DMEM)和哈姆F12培养基按1:1混合组成的无血清组织培养基在此显示可在培养数天内支持鲁伯H - 35细胞生长。细胞最初接种于含血清的DMEM培养基中3小时。细胞贴壁后,去除血清并用这两种市售组织培养基的无血清1:1混合物替换。在最初5天,在低密度接种培养中,这种未添加其他成分的无血清培养基中细胞生长的倍增时间为46小时。添加转铁蛋白(5微克/毫升)和胰岛素(3.3纳摩尔)后,细胞倍增时间为17小时,这与含10%胎牛血清的培养基中的生长速率相当。在无转铁蛋白的情况下,无血清培养基中的生长速率与培养物的细胞密度相关。高密度无血清培养的条件培养基在受体低密度接种培养中有生长刺激活性。这种简单的无血清培养基将有助于对H - 35大鼠肝癌细胞生长调控的研究。