Lesma E, Di Giulio A M, Ferro L, Prino G, Gorio A
Laboratory for Research on Pharmacology of Neurodegenerative Disorders, Dept. Medical Pharmacology, Milano, Italy.
J Neurosci Res. 1996 Dec 1;46(5):565-71. doi: 10.1002/(SICI)1097-4547(19961201)46:5<565::AID-JNR5>3.0.CO;2-H.
This study has shown that glycosaminoglycans added to the culture medium may affect neurite formation in SH-SY5Y neuroblastoma cells. The most effective glycosaminoglycans are heparin and COS 8, a preparation with low anticoagulant activity. Promotion of neuritogenesis was remarkable at concentrations as low as 10(-8) and 10(-10). When added at 10(-4) M both agents are inhibitory. Chondroitin-4 sulfate, dermatan sulfate, and heparan sulfate were also effective, the doses required were, however, as high as 10(-4) M for promoting and 10(-4) M for inhibiting neuritogenesis. Thereby low doses of glycosaminoglycans promote, while higher doses inhibit neurite formation. The effects were observed when neuritogenesis was promoted in neuroblastoma cultures either by deprivation of serum or by addition of retinoic acid, in the former case neuritogenesis occurred within 48 hr; in the latter, in 14 days. PC12 pheochromocytoma cells neuritogenesis was triggered by adding NGF to the culture medium. We have also observed that glycosaminoglycan supplementation to the culture medium lowered the quantity of NGF required to form neurites by PC12 cells. Glycosaminoglycans at the dose of 10(-8) M allow the formation of PC12 neurites even in presence of 1 ng/ml NGF, a dose that normally is ineffective.
本研究表明,添加到培养基中的糖胺聚糖可能会影响SH-SY5Y神经母细胞瘤细胞的神经突形成。最有效的糖胺聚糖是肝素和COS 8(一种抗凝活性低的制剂)。在低至10^(-8)和10^(-10)的浓度下,神经突生成的促进作用就很显著。当以10^(-4) M添加时,这两种物质均具有抑制作用。硫酸软骨素-4、硫酸皮肤素和硫酸乙酰肝素也有效,然而,促进神经突生成所需的剂量高达10^(-4) M,抑制神经突生成所需的剂量也为10^(-4) M。因此,低剂量的糖胺聚糖促进神经突形成,而高剂量则抑制神经突形成。当通过血清剥夺或添加视黄酸在神经母细胞瘤培养物中促进神经突生成时,观察到了这种效应,在前一种情况下,神经突生成在48小时内发生;在后一种情况下,在14天内发生。PC12嗜铬细胞瘤细胞的神经突生成是通过向培养基中添加神经生长因子(NGF)触发的。我们还观察到,向培养基中补充糖胺聚糖降低了PC12细胞形成神经突所需的NGF量。10^(-8) M剂量的糖胺聚糖即使在存在1 ng/ml NGF(通常无效的剂量)的情况下也能使PC12神经突形成。