Tedeschi B, Wilson D L
J Neurosci. 1983 Sep;3(9):1728-34. doi: 10.1523/JNEUROSCI.03-09-01728.1983.
From 1 to 28 days after frog sciatic nerve damage, dorsal root ganglia were incubated with [35S] methionine, and the labeled, rapidly transported proteins at various points along the nerve were analyzed on two-dimensional gels. The results show a dramatic increase in the labeling of a protein, which we have designated as A25, only after the arrival of the rapidly transported proteins at regenerating nerve tips. This effect is first seen 3 to 5 days after injury. On gels from regenerating nerves, A25 appears as a series of intense spots with an apparent molecular weight of 70,000. A25 is retrogradely transported from the regenerating nerve tip regions. Since labeled A25 increases only after the rapidly transported proteins reach regions of nerve containing regenerating axons, we conclude that it most likely arises from post-translational modification of a transported protein. Various experiments were conducted to rule out alternative sources of A25 labeling at the nerve periphery.
在青蛙坐骨神经损伤后的1至28天内,将背根神经节与[35S]甲硫氨酸一起孵育,并在二维凝胶上分析沿神经不同部位标记的快速运输蛋白。结果显示,只有在快速运输蛋白到达再生神经末梢后,一种我们命名为A25的蛋白的标记才会急剧增加。这种效应在损伤后3至5天首次出现。在再生神经的凝胶上,A25表现为一系列明显分子量为70,000的密集斑点。A25从再生神经末梢区域逆向运输。由于标记的A25仅在快速运输蛋白到达含有再生轴突的神经区域后增加,我们得出结论,它很可能来自运输蛋白的翻译后修饰。进行了各种实验以排除神经外周A25标记的其他来源。