Carine K, Schengrund C L
J Neurosci Res. 1984;12(1):59-69. doi: 10.1002/jnr.490120106.
The effects of exogenous GM1 and GD1a on S20Y murine neuroblastoma cells were assessed by monitoring morphology, tumorigenicity, mitotic index, and plating efficiency. S20Y cells were seeded at a density equivalent to 5 X 10(4) cells per 35-mm tissue culture dish; 38-42 hr after seeding (preconfluent stage) the cells were treated for 12 hr with 100 micrograms of ganglioside per ml of medium in which the serum content was reduced from 10% to 0.5%. Analysis of the cell lipids indicated that added ganglioside became tightly associated with the membrane during the 12-hr exposure. GM1 treatment resulted in increased projections on the cell surface and fine structures projecting from the cell processes. GD1a treatment resulted in a reduction in the cellular mitotic index. Plating efficiency was reduced by both GM1 and GD1a. Neither ganglioside affected tumorigenicity of the S20Y cells. Twelve hours after removal of the added ganglioside and exposure of the cells to normal medium, the ganglioside composition of the membranes from treated cells approached that of the controls, and the ganglioside-induced effects had been reversed. These results suggest that addition of specific gangliosides induces different cellular responses and that these changes are dependent upon the continued presence of the ganglioside.
通过监测形态、致瘤性、有丝分裂指数和平板接种效率,评估外源性GM1和GD1a对S20Y小鼠神经母细胞瘤细胞的影响。将S20Y细胞以相当于每35毫米组织培养皿5×10(4)个细胞的密度接种;接种后38 - 42小时(汇合前期),用每毫升培养基含100微克神经节苷脂处理细胞12小时,培养基中的血清含量从10%降至0.5%。细胞脂质分析表明,在12小时的暴露期间,添加的神经节苷脂与细胞膜紧密结合。GM1处理导致细胞表面突起增加以及从细胞突起伸出的精细结构。GD1a处理导致细胞有丝分裂指数降低。GM1和GD1a均降低了平板接种效率。两种神经节苷脂均未影响S20Y细胞的致瘤性。去除添加的神经节苷脂并将细胞暴露于正常培养基12小时后,处理过的细胞的细胞膜神经节苷脂组成接近对照细胞,且神经节苷脂诱导的效应已逆转。这些结果表明,添加特定的神经节苷脂会诱导不同的细胞反应,且这些变化取决于神经节苷脂的持续存在。