Ingoglia N A, Sturman J A, Jaggard P, Perez C
Brain Res. 1982 Apr 29;238(2):341-51. doi: 10.1016/0006-8993(82)90109-3.
Experiments were designed to determine whether polyamines are bound to 4S RNA and then transported axonally along regenerating optic axons of goldfish. In one set of experiments, inhibition of retinal RNA synthesis by intraocular injections of 10 microgram of cordycepin, blocked the axonal transport of both [3H]RNA and [14C]spermidine by about 65%, 6 and 14 days after injection. Intraocular injections of vinblastine, (0.1, 0.5 or 1.0 microgram) an agent which interrupts axonal transport of proteins, had no effect on retinal RNA synthesis nor on the amount of [14C]spermidine incorporated into the TCA-insoluble fraction of retinal extracts. However, the axonal transport of both [3H]RNA and [14C]polyamines was affected in a dose-dependent fashion; the inhibition of both was approximately 80% at the higher dose. Further evidence for an association between axonally transported 4S RNA and polyamines came from experiments in which regenerating optic axons were cut and allowed to degenerate 6 days after injection of [3H]spermidine into the eye. The loss of optic axons from the tectum 7 days after cutting the nerve resulted in an 86% loss of TCA insoluble polyamines, indicating a largely intra-axonal locus. A similar loss of 4S RNA was found in identical experiments following injections of [3H]uridine into the eye. Finally, experiments were performed in which [3H]spermidine was injected into both eyes of 12 fish whose optic nerves had been regenerating for 18 days. Six days later, fish were sacrificed and RNA was extracted from tectal homogenates by hot phenol and ethanol precipitation. The major stable RNA species were separated by SDS-polyacrylamide disc gel electrophoresis and radioactivity was determined by extraction of 2.0 mm gel slices. Results showed co-migration of 3H with 4S RNA optical density peaks, and not with 28S and 18S ribosomal RNA peaks, suggesting that some polyamine-associated radioactivity is bound to axonally transported 4S RNA. When the nature of that radioactivity was determined on an amino acid analyzer, it was found to be present primarily as spermine and not as the injected compound spermidine. The data are consistent with the hypothesis that some spermine is bound to 4S RNA and then axonally transported along regenerating axons of the goldfish optic nerve.
设计实验以确定多胺是否与4S RNA结合,然后沿金鱼再生的视神经轴突进行轴突运输。在一组实验中,眼内注射10微克的放线菌素D抑制视网膜RNA合成,在注射后6天和14天,[3H]RNA和[14C]亚精胺的轴突运输被阻断约65%。眼内注射长春花碱(0.1、0.5或1.0微克),一种中断蛋白质轴突运输的药物,对视网膜RNA合成以及掺入视网膜提取物三氯乙酸不溶性部分的[14C]亚精胺量均无影响。然而,[3H]RNA和[14C]多胺的轴突运输均受到剂量依赖性影响;在较高剂量下,两者的抑制率约为80%。轴突运输的4S RNA与多胺之间存在关联的进一步证据来自以下实验:在向眼内注射[3H]亚精胺后6天,切断再生的视神经并使其退化。切断神经7天后,视叶中视神经轴突的损失导致三氯乙酸不溶性多胺损失86%,表明其主要位于轴突内。在向眼内注射[3H]尿苷后的相同实验中,发现4S RNA也有类似的损失。最后,对12条视神经已再生18天的鱼的双眼注射[3H]亚精胺进行实验。6天后,处死鱼,通过热酚和乙醇沉淀从视叶匀浆中提取RNA。通过SDS-聚丙烯酰胺圆盘凝胶电泳分离主要的稳定RNA种类,并通过提取2.0毫米凝胶切片测定放射性。结果显示3H与4S RNA光密度峰共迁移,而不与28S和18S核糖体RNA峰共迁移,这表明一些与多胺相关的放射性与轴突运输的4S RNA结合。当在氨基酸分析仪上确定该放射性的性质时,发现其主要以精胺形式存在,而不是以注射的化合物亚精胺形式存在。这些数据与以下假设一致:一些精胺与4S RNA结合,然后沿金鱼视神经的再生轴突进行轴突运输。