Lasek R J, Gainer H, Przybylski R J
Proc Natl Acad Sci U S A. 1974 Apr;71(4):1188-92. doi: 10.1073/pnas.71.4.1188.
The squid giant axon is presented as a model for the study of macromolecular interaction between cells in the nervous system. When the isolated giant axon was incubated in sea water containing [(3)H]leucine for 0.5-5 hr, newly synthesized proteins appeared in the sheath and axoplasm as demonstrated by: (i) radioautography, (ii) separation of the sheath and axoplasm by extrusion, and (iii) perfusion of electrically excitable axons. The absence of ribosomal RNA in the axoplasm [Lasek, R. J. et al. (1973) Nature 244, 162-165] coupled with other evidence indicates that the labeled proteins that are found in the axoplasm originate in the Schwann cells surrounding the axon. Approximately 50% of the newly synthesized Schwann cell proteins are transferred to the giant axon. These transferred proteins are soluble for the most part and range in molecular size from 12,000 to greater than 200,000 daltons. It is suggested that proteins transferred from the Schwann cell to the axon have a regulatory role in neuronal function.
乌贼巨大轴突被作为研究神经系统中细胞间大分子相互作用的模型。当将分离出的巨大轴突在含有[³H]亮氨酸的海水中孵育0.5 - 5小时时,新合成的蛋白质出现在髓鞘和轴质中,这通过以下方法得以证明:(i)放射自显影,(ii)通过挤压分离髓鞘和轴质,以及(iii)对电可兴奋轴突进行灌注。轴质中不存在核糖体RNA[拉塞克,R.J.等人(1973年)《自然》244,162 - 165]以及其他证据表明,在轴质中发现的标记蛋白质起源于轴突周围的施万细胞。大约50%新合成的施万细胞蛋白质被转移到巨大轴突中。这些转移的蛋白质大部分是可溶的,分子大小范围从12,000到大于200,000道尔顿。有人提出,从施万细胞转移到轴突的蛋白质在神经元功能中具有调节作用。