Fuks B B, Sterlina A G, Zaraĭskiĭ E I, Stepanov A A
Biull Eksp Biol Med. 1985 Apr;99(4):474-6.
Thymic gangliosides GM3 and GD3 and LacCer incorporated into the membrane of the tumor target cell leukemia (YAC) increase its sensitivity to the membrane toxic action of spleen effectors. Unlike thymic gangliosides GD3, ganglioside GD3 of the brain origin substantially reduces tumor cell sensitivity to spleen effectors. Some other brain glycosphingolipids differing essentially in the structure of the carbohydrate part of the molecule exert the same action. It has been shown in model experiments with incorporation into the tumor cell membrane of brain ganglioside GD3 combined with thymic LacCer or with egg phosphatidylcholine that the increase in the sensitivity of the tumor cell membrane to spleen effectors is linked with a change in the properties of the lipid membrane matrix under the effect of unsaturated fatty acids (e.g. in experiments with phosphatidylcholine). It follows from the data presented that the capability of influencing the sensitivity of tumor cells to natural spleen effectors largely depends on the differences in the structure of the cearamide part of brain and thymic GD3.
掺入肿瘤靶细胞白血病(YAC)膜中的胸腺神经节苷脂GM3、GD3和乳糖神经酰胺可提高其对脾效应细胞膜毒性作用的敏感性。与胸腺神经节苷脂GD3不同,脑源性神经节苷脂GD3会显著降低肿瘤细胞对脾效应细胞的敏感性。分子碳水化合物部分结构存在本质差异的其他一些脑糖鞘脂也有同样的作用。在将脑源性神经节苷脂GD3与胸腺乳糖神经酰胺或卵磷脂掺入肿瘤细胞膜的模型实验中表明,肿瘤细胞膜对脾效应细胞敏感性的提高与不饱和脂肪酸作用下脂质膜基质性质的改变有关(如在卵磷脂实验中)。从所呈现的数据可以看出,影响肿瘤细胞对天然脾效应细胞敏感性的能力很大程度上取决于脑源性和胸腺源性GD3神经酰胺部分结构的差异。