Tanner S L, Storm E E, Bittner G D
Department of Zoology, University of Texas, Austin 78712.
J Neurosci. 1995 Jan;15(1 Pt 2):540-8. doi: 10.1523/JNEUROSCI.15-01-00540.1995.
Protein maintenance and degradation are examined in the severed distal (anucleate) portions of crayfish medial giant axons (MGAs), which remain viable for over 7 months following axotomy. On polyacrylamide gels, the silver-stained protein banding pattern of anucleate MGAs severed from their cell bodies for up to 4 months remains remarkably similar to that of intact MGAs. At 7 months postseverance, some (but not all) proteins are decreased in anucleate MGAs compared to intact MGAs. To determine the half-life of axonally transported proteins, we radiolabeled MGA cell bodies and monitored the degradation of newly synthesized transported proteins. Assuming exponential decay, proteins in the fast component of axonal transport have an average half-life of 14 d in anucleate MGAs and proteins in the slow component have an average half-life of 17 d. Such half-lives are very unlikely to account for the ability of anucleate MGAs to survive for over 7 months after axotomy.
在小龙虾内侧巨轴突(MGA)被切断的远端(无核)部分研究蛋白质的维持和降解情况,这些部分在轴突切断后可存活超过7个月。在聚丙烯酰胺凝胶上,从其细胞体切断长达4个月的无核MGA的银染蛋白条带模式与完整MGA的模式非常相似。在切断后7个月时,与完整MGA相比,无核MGA中的一些(但不是全部)蛋白质减少。为了确定轴突运输蛋白的半衰期,我们用放射性标记MGA细胞体并监测新合成的运输蛋白的降解。假设呈指数衰减,轴突运输快速成分中的蛋白质在无核MGA中的平均半衰期为14天,慢速成分中的蛋白质平均半衰期为17天。这样的半衰期极不可能解释无核MGA在轴突切断后存活超过7个月的能力。