Agy P C, Shipley G D, Ham R G
In Vitro. 1981 Aug;17(8):671-80. doi: 10.1007/BF02628402.
An optimized medium, designated MCDB 411, has been developed for mouse neuroblastoma cells. At cell densities of 1 x 10(4) cells/cm2 or greater, several different clones of C1300 mouse neuroblastoma cells can be cultured serially in Medium MCDB 411 with no serum or other undefined supplementation and with a doubling time of about 24 h. At clonal densities it is necessary to supplement the medium with 1.0 micrograms/ml insulin. Alternately, good clonal growth can be obtained without direct supplementation by coating the culture dishes with insulin and rinsing off all that is not tightly bound. Primary cultures of cells from serially transplanted C1300 tumors that have never been cultured previously in vitro can be established directly in unsupplemented Medium MCDB 411 with rapid initiation of multiplication and no apparent crisis or selection for minority cell types. The availability of a synthetic medium that supports growth of neuroblastoma cells without supplementation should facilitate the use of these cells as model systems for the study of neuronal function and differentiation.
已开发出一种名为MCDB 411的优化培养基用于小鼠神经母细胞瘤细胞。在细胞密度为1×10⁴个细胞/平方厘米或更高时,几种不同克隆的C1300小鼠神经母细胞瘤细胞可以在不含血清或其他未定义补充剂的MCDB 411培养基中连续培养,倍增时间约为24小时。在克隆密度下,有必要向培养基中添加1.0微克/毫升胰岛素。或者,通过用胰岛素包被培养皿并冲洗掉所有未紧密结合的物质,无需直接添加也可获得良好的克隆生长。从未在体外培养过的经连续移植的C1300肿瘤细胞的原代培养物,可以直接在未补充的MCDB 411培养基中建立,细胞能迅速开始增殖,且没有明显的危机或对少数细胞类型的选择。一种无需补充就能支持神经母细胞瘤细胞生长的合成培养基的出现,应有助于将这些细胞用作研究神经元功能和分化的模型系统。