Spoerri P E, Roisen F J
Department of Anatomical Sciences and Neurobiology, University of Louisville, KY 40292.
Neurosci Lett. 1988 Jul 19;90(1-2):21-6. doi: 10.1016/0304-3940(88)90780-x.
The ability of gangliosides to potentiate nerve growth factor (NGF)-independent trophic agents was determined by examining the capacity of an exogenous mixture of bovine brain gangliosides (BBG) and the monosialoganglioside GM1 to enhance the neuritogenic action of conditioned media (CM). CM were prepared with cultures of C6 glioma cells, neonatal rat astroglial cells, rat L6 myoblasts and chick embryonic skeletal muscle. Chick embryonic (9 day) dorsal root ganglia (DRG) were cultured on collagen-coated surfaces. The nutrient media with serum added or serum-free N1 medium were supplemented with 50% of one of the CM with or without BBG (150 micrograms/ml) or GM1 (150 micrograms/ml). The neuritogenic responses of DRG 48 h in vitro were evaluated microscopically on the basis of neurite length and number. The neurite promoting action of the factor(s) present in the various CM was potentiated by BBG or GM1 and resulted in increased neurite length and number.
通过检测牛脑神经节苷脂(BBG)和单唾液酸神经节苷脂GM1的外源混合物增强条件培养基(CM)促神经突生长作用的能力,来确定神经节苷脂增强非神经生长因子(NGF)依赖性营养因子的能力。CM由C6胶质瘤细胞、新生大鼠星形胶质细胞、大鼠L6成肌细胞和鸡胚骨骼肌培养物制备。鸡胚(9日龄)背根神经节(DRG)培养于胶原包被的表面。添加血清的营养培养基或无血清N1培养基补充50%含有或不含有BBG(150微克/毫升)或GM1(150微克/毫升)的CM之一。体外48小时后,根据神经突长度和数量,通过显微镜评估DRG的促神经突反应。BBG或GM1增强了各种CM中存在的因子的促神经突作用,并导致神经突长度和数量增加。