Sonderegger P, Fishman M C, Bokoum M, Bauer H C, Neale E A, Nelson P G
J Cell Biol. 1984 Jan;98(1):364-8. doi: 10.1083/jcb.98.1.364.
A series of proteins putatively involved in the generation of axonal diversity was identified. Neurons from ventral spinal cord and dorsal root ganglia were grown in a compartmented cell-culture system which offers separate access to cell somas and axons. The proteins synthesized in the neuronal cell somas and subsequently transported into the axons were selectively analyzed by 2-dimensional gel electrophoresis. The patterns of axonal proteins were substantially less complex than those derived from the proteins of neuronal cell bodies. The structural and functional similarity of axons from different neurons was reflected in a high degree of similarity of the gel pattern of the axonal proteins from sensory ganglia and spinal cord neurons. Each axonal type, however, had several proteins that were markedly less abundant or absent in the other. These neuron-population enriched proteins may be involved in the implementation of neuronal diversity. One of the proteins enriched in dorsal root ganglia axons had previously been found to be expressed with decreased abundance when dorsal root ganglia axons were co-cultured with ventral spinal cord cells under conditions in which synapse formation occurs (P. Sonderegger, M. C. Fishman, M. Bokoum, H. C. Bauer, and P.G. Nelson, 1983, Science [Wash. DC], 221:1294-1297). This protein may be a candidate for a role in growth cone functions, specific for neuronal subsets, such as pathfinding and selective axon fasciculation or the initiation of specific synapses. The methodology presented is thus capable of demonstrating patterns of protein synthesis that distinguish different neuronal subsets. The accessibility of these proteins for structural and functional studies may contribute to the elucidation of neuron-specific functions at the molecular level.
鉴定出一系列可能参与轴突多样性生成的蛋白质。来自腹侧脊髓和背根神经节的神经元在一个分隔的细胞培养系统中生长,该系统可分别接触细胞体和轴突。通过二维凝胶电泳选择性分析在神经元细胞体中合成并随后转运到轴突中的蛋白质。轴突蛋白的模式比源自神经元细胞体的蛋白质模式要简单得多。来自不同神经元的轴突在结构和功能上的相似性反映在感觉神经节和脊髓神经元轴突蛋白的凝胶模式高度相似。然而,每种轴突类型都有几种在其他类型中明显含量较低或不存在的蛋白质。这些神经元群体富集的蛋白质可能参与神经元多样性的实现。先前发现,当背根神经节轴突在发生突触形成的条件下与腹侧脊髓细胞共培养时,一种在背根神经节轴突中富集的蛋白质表达量会降低(P. 桑德雷格、M.C. 菲什曼、M. 博库姆、H.C. 鲍尔和P.G. 纳尔逊,1983年,《科学》[华盛顿特区],221:1294 - 1297)。这种蛋白质可能是在生长锥功能中起作用的候选蛋白,对特定的神经元亚群具有特异性,例如路径寻找、选择性轴突束集或特定突触的起始。因此,所介绍的方法能够展示区分不同神经元亚群的蛋白质合成模式。这些蛋白质用于结构和功能研究的可及性可能有助于在分子水平阐明神经元特异性功能。