Bragg D C, Meeker R B, Duff B A, English R V, Tompkins M B
Curriculum in Neurobiology and Department of Neurology, University of North Carolina, Chapel Hill, NC 27599, USA.
Brain Res. 1999 Jan 23;816(2):431-7. doi: 10.1016/s0006-8993(98)01177-9.
The neurotoxic effects of the feline immunodeficiency virus (FIV) and FIV envelope proteins were measured in primary cultures of feline cortical neurons. Envelope protein from the FIV-PPR strain promoted neuronal swelling and death, whereas envelope protein from the FIV-34TF10 isolate produced intermediate or negligible toxicity. No effect was observed in control cultures treated with envelope protein from the Epstein-Barr virus. A concentration-effect curve showed that FIV-PPR protein produced maximal toxicity at 200 pM protein and decreased toxicity at higher concentrations, which is consistent with previous reports of the HIV-1 surface glycoprotein, gp120. These effects required the presence of low concentrations of glutamate. Using the natural host cells as targets, the effects of envelope protein and infectious virions were directly compared. All of the toxic activity could be attributed to non-infectious interactions between the viral envelope and target cells. Addition of 1 microM tetrodotoxin failed to block the effects of FIV-PPR in the presence of 20 microM glutamate. Toxicity would appear to involve two steps in which the envelope protein first sensitizes neurons through non-synaptic interactions (TTX insensitive) thereby setting the stage for enhanced synaptic activation via glutamate receptors (TTX sensitive).
在猫皮层神经元原代培养物中测定了猫免疫缺陷病毒(FIV)及其包膜蛋白的神经毒性作用。FIV-PPR株的包膜蛋白可促进神经元肿胀和死亡,而FIV-34TF10分离株的包膜蛋白产生的毒性中等或可忽略不计。用爱泼斯坦-巴尔病毒包膜蛋白处理的对照培养物未观察到影响。浓度-效应曲线表明,FIV-PPR蛋白在200 pM蛋白时产生最大毒性,在更高浓度时毒性降低,这与先前关于HIV-1表面糖蛋白gp120的报道一致。这些效应需要低浓度谷氨酸的存在。以天然宿主细胞为靶标,直接比较了包膜蛋白和感染性病毒粒子的作用。所有毒性活性都可归因于病毒包膜与靶细胞之间的非感染性相互作用。在存在20 μM谷氨酸的情况下,添加1 μM河豚毒素未能阻断FIV-PPR的作用。毒性似乎涉及两个步骤,其中包膜蛋白首先通过非突触相互作用(对河豚毒素不敏感)使神经元敏感,从而为通过谷氨酸受体增强突触激活(对河豚毒素敏感)奠定基础。