Lasek R J, Gainer H, Barker J L
J Cell Biol. 1977 Aug;74(2):501-23. doi: 10.1083/jcb.74.2.501.
The hypothesis that glial cells synthesize proteins which are transferred to adjacent neurons was evaluated in the giant fiber of the squid (Loligo pealei). When giant fibers are separated from their neuron cell bodies and incubated in the presence of radioactive amino acids, labeled proteins appear in the glial cells and axoplasm. Labeled axonal proteins were detected by three methods: extrusion of the axoplasm from the giant fiber, autoradiography, and perfusion of the giant fiber. This protein synthesis is completely inhibited by puromycin but is not affected by chloramphenicol. The following evidence indicates that the labeled axonal proteins are not synthesized within the axon itself. (a) The axon does not contain a significant amount of ribosomes or ribosomal RNA. (b) Isolated axoplasm did not incorporate [(3)H]leucine into proteins. (c) Injection of Rnase into the giant axon did not reduce the appearance of newly synthesized proteins in the axoplasm of the giant fiber. These findings, coupled with other evidence, have led us to conclude that the adaxonal glial cells synthesize a class of proteins which are transferred to the giant axon. Analysis of the kinetics of this phenomenon indicates that some proteins are transferred to the axon within minutes of their synthesis in the glial cells. One or more of the steps in the transfer process appear to involve Ca++, since replacement of extracellular Ca++ by either Mg++ or Co++ significantly reduces the appearance of labeled proteins in the axon. A substantial fraction of newly synthesized glial proteins, possibly as much as 40 percent, are transferred to the giant axon. These proteins are heterogeneous and range in size from 12,000 to greater than 200,000 daltons. Comparisons of the amount of amino acid incorporation in glia cells and neuron cell bodies raise the possibility that the adaxonal glial cells may provide an important source of axonal proteins which is supplemental to that provided by axonal transport from the cell body. These findings are discussed with reference to a possible trophic effect of glia on neurons and metabolic cooperation between adaxonal glia and the axon.
在枪乌贼(Loligo pealei)的巨纤维中,对神经胶质细胞合成可转移至相邻神经元的蛋白质这一假说进行了评估。当巨纤维与其神经元细胞体分离,并在放射性氨基酸存在的情况下进行孵育时,标记的蛋白质出现在神经胶质细胞和轴质中。通过三种方法检测到了标记的轴突蛋白:从巨纤维中挤出轴质、放射自显影以及对巨纤维进行灌注。这种蛋白质合成完全被嘌呤霉素抑制,但不受氯霉素影响。以下证据表明标记的轴突蛋白并非在轴突自身内合成。(a) 轴突不含大量核糖体或核糖体RNA。(b) 分离出的轴质未将[³H]亮氨酸掺入蛋白质中。(c) 向巨轴突中注射核糖核酸酶并未减少巨纤维轴质中新合成蛋白质的出现。这些发现,再加上其他证据,使我们得出结论:轴旁神经胶质细胞合成一类蛋白质并转移至巨轴突。对这一现象动力学的分析表明,一些蛋白质在神经胶质细胞中合成后几分钟内就被转移至轴突。转移过程中的一个或多个步骤似乎涉及钙离子,因为用镁离子或钴离子替代细胞外钙离子会显著减少轴突中标记蛋白质的出现。相当一部分新合成的神经胶质细胞蛋白质,可能高达40%,被转移至巨轴突。这些蛋白质具有异质性,大小范围从12,000道尔顿到大于200,000道尔顿。对神经胶质细胞和神经元细胞体中氨基酸掺入量的比较,增加了轴旁神经胶质细胞可能是轴突蛋白质重要来源的可能性,这是对从细胞体进行轴突运输所提供来源的补充。结合神经胶质细胞对神经元可能的营养作用以及轴旁神经胶质细胞与轴突之间的代谢协作,对这些发现进行了讨论。