Koike H, Matsumoto H, Umitsu Y
Department of Neurophysiology, Tokyo Metropolitan Institute for Neurosciences, Japan.
Neuroscience. 1989;32(2):539-55. doi: 10.1016/0306-4522(89)90100-0.
Substance-specific selective axonal transport was examined in a single axon by injecting [3H]leucine and [14C]acetylcholine simultaneously into the cell body of a giant cholinergic neuron (R2) in the abdominal ganglion of Aplysia kurodai. The ganglion and attached nerves were cultured for several hours after the injection and the migration of radioactive substances along the axons of the injected neuron was examined. The substances examined were 3H labeled membrane proteins and soluble proteins synthesized in the cell body, 14C labeled bound acetylcholine formed in the cell, injected [3H]leucine and soluble [14C]acetylcholine. Membrane proteins and bound acetylcholine (plus a part of soluble acetylcholine) moved along the axon somatofugally at maximum velocities of 2.4 and 1.7 mm/h, respectively, at 25 degrees C. Soluble proteins, free leucine and most of the soluble acetylcholine did not move by fast axonal transport but diffused inside the axon of the neuron R2 at rates predicted from their expected diffusion constants in the axoplasm [Koike H. and Nagata Y. (1979) J. Physiol. 295, 397-417]. The diffusion kinetics of these substances were analysed and used for determination of true axon length, and to separate axonal transport components from diffusing components. An antimitotic drug, colchicine, selectively suppressed the axonal transport of membrane proteins but not of acetylcholine at 1-5 mM concentration, though it finally blocked the axonal transport of acetylcholine at 20 mM. When 1-5 mM colchicine was separately perfused only to the distal axon of the neuron R2, the migration of membrane proteins was stopped just proximal to the colchicine perfusion zone but acetylcholine migration was not disturbed by the drug. The moving component of acetylcholine was recovered by sucrose density centrifugation from a compartment previously reported as that of vesicular acetylcholine. As a possible mechanism of this selective axonal transport, it is proposed that there are two groups of microtubules: a colchicine-sensitive group of microtubules which may transport membrane proteins, and a colchicine-resistant group which may preferentially transport the transmitter substance acetylcholine at a slower rate.
通过将[3H]亮氨酸和[14C]乙酰胆碱同时注入黑背海兔腹神经节中一个巨大的胆碱能神经元(R2)的细胞体,在单根轴突中研究了物质特异性的选择性轴突运输。注射后,将神经节和相连的神经培养数小时,并检测放射性物质沿注入神经元轴突的迁移情况。所检测的物质包括在细胞体中合成的3H标记的膜蛋白和可溶性蛋白、在细胞中形成的14C标记的结合乙酰胆碱、注入的[3H]亮氨酸和可溶性[14C]乙酰胆碱。在25℃时,膜蛋白和结合乙酰胆碱(加上一部分可溶性乙酰胆碱)分别以2.4和1.7mm/h的最大速度沿轴突向胞体方向移动。可溶性蛋白、游离亮氨酸和大部分可溶性乙酰胆碱并非通过快速轴突运输移动,而是以根据其在轴浆中预期扩散常数预测的速率在神经元R2的轴突内扩散[小池浩和永田洋(1979年)《生理学杂志》295卷,397 - 417页]。分析了这些物质的扩散动力学,并用于确定轴突的真实长度,以及将轴突运输成分与扩散成分区分开来。一种抗有丝分裂药物秋水仙碱在1 - 5mM浓度下选择性地抑制膜蛋白的轴突运输,但不抑制乙酰胆碱的轴突运输,不过在20mM时最终会阻断乙酰胆碱的轴突运输。当仅将1 - 5mM秋水仙碱分别灌注到神经元R2的远端轴突时,膜蛋白的迁移在秋水仙碱灌注区近端停止,但乙酰胆碱的迁移不受该药物干扰。通过蔗糖密度离心从先前报道为囊泡乙酰胆碱所在的区室中回收了乙酰胆碱的移动成分。作为这种选择性轴突运输的一种可能机制,有人提出存在两组微管:一组对秋水仙碱敏感的微管,可能运输膜蛋白;另一组对秋水仙碱有抗性的微管,可能以较慢的速率优先运输递质乙酰胆碱。