Katoh-Semba R, Facci L, Skaper S D, Varon S
J Cell Physiol. 1986 Jan;126(1):147-53. doi: 10.1002/jcp.1041260120.
Previous studies with microcultures of astroglial (AG) cells from newborn rat cerebrum had shown an ability of gangliosides to interact with AG cells cultured under defined conditions. We have now investigated the capability of gangliosides to stimulate DNA synthesis and cell number increases in similar secondary microcultures of newborn rat cerebrum AG cells. At a concentration of 6 X 10(-5)M, GM1 ganglioside stimulated DNA synthesis and increased cell numbers, with DNA synthesis leading cell increases by 12-24 hr. The ganglioside-induced AG cell proliferative response occurred with GD1a, GD1b and GT1b, GT1b being the most potent at 10(-5)M--while asialo GM1 and sialic acid were without effect. In the standard test cultures, DNA synthesis declined very steeply after the first day, with cell numbers stabilizing at the level reached after 2 days. Ganglioside was not itself responsible for the restricted proliferative response, as serum produced the same behaviors.
先前对新生大鼠大脑星形胶质细胞(AG)微培养物的研究表明,神经节苷脂能够与在特定条件下培养的AG细胞相互作用。我们现在研究了神经节苷脂在新生大鼠大脑AG细胞类似的第二代微培养物中刺激DNA合成和增加细胞数量的能力。在浓度为6×10⁻⁵M时,GM1神经节苷脂刺激DNA合成并增加细胞数量,DNA合成导致细胞数量在12 - 24小时后增加。神经节苷脂诱导的AG细胞增殖反应在GD1a、GD1b和GT1b中也会发生,GT1b在10⁻⁵M时最有效,而脱唾液酸GM1和唾液酸则没有效果。在标准测试培养物中,DNA合成在第一天后急剧下降,细胞数量在2天后达到的水平稳定下来。神经节苷脂本身并不是增殖反应受限的原因,因为血清也产生相同的行为。