Sciannamblo Mariateresa, Chigorno Vanna, Passi Alberto, Valaperta Rea, Zucchi Ileana, Sonnino Sandro
Study Center for the Biochemistry and Biotechnology of Glycolipids, Department of Medical Chemistry, Biochemistry and Biotechnology, University of Milan, Segrate, Italy.
Glycoconj J. 2002 Mar;19(3):181-6. doi: 10.1023/A:1024249707516.
In this study we show that the ganglioside content and pattern of human skin fibroblasts change along the process of cell subculture progression by varying the cell density. GM3, GD3 and GD1a were components of the total cell ganglioside mixtures extracted from cells, but GD1a was in all the extracts a minor component or very scant. Other gangliosides present in traces were not characterised. The fibroblast ganglioside content of 52 pools of cells obtained from 5 different cell lines cultured at variable cell density ranged from 2.0 to 13.1 nmoles per mg of cell protein. The molar ratio between GM3 and GD3 varied from 418 to 0.6 in the ganglioside mixtures, as determined by densitometric quantitative analysis after thin layer chromatographic separation. Both the ganglioside content and the GM3/GD3 molar ratio were constant along several passages of subculture progression performed by plating cells collected at confluence. Instead, when the subculture progression was performed by plating cells collected at a few days after reaching confluence, a progressive increase of the ganglioside content was observed. GD3 increased proportionally more than GM3 so that a progressive decrease of the ratio between GM3 and GD3 was observed. In some experiments, GD3 was very scant at the beginning of the progression, while it was near 30% after 5 passages under these conditions. The progressive increase of GD3 along the high density cell population subculture progression was associated to a moderate increase of the mRNA GD3 synthase.
在本研究中,我们表明,通过改变细胞密度,人皮肤成纤维细胞的神经节苷脂含量和模式会随着细胞传代培养进程而发生变化。GM3、GD3和GD1a是从细胞中提取的总细胞神经节苷脂混合物的成分,但GD1a在所有提取物中都是次要成分或含量极少。其他痕量存在的神经节苷脂未作鉴定。从5种不同细胞系在可变细胞密度下培养获得的52组细胞的成纤维细胞神经节苷脂含量范围为每毫克细胞蛋白2.0至13.1纳摩尔。通过薄层色谱分离后的光密度定量分析测定,神经节苷脂混合物中GM3与GD3的摩尔比在418至0.6之间变化。在通过接种汇合时收集的细胞进行的几次传代培养进程中,神经节苷脂含量和GM3/GD3摩尔比均保持恒定。相反,当通过接种汇合后几天收集的细胞进行传代培养进程时,观察到神经节苷脂含量逐渐增加。GD3的增加比例超过GM3,因此观察到GM3与GD3的比例逐渐降低。在一些实验中,GD3在进程开始时含量极少,而在这些条件下传代5次后接近30%。GD3沿高密度细胞群体传代培养进程的逐渐增加与mRNA GD3合酶的适度增加相关。