Hoffman P N, Thompson G W, Griffin J W, Price D L
J Cell Biol. 1985 Oct;101(4):1332-40. doi: 10.1083/jcb.101.4.1332.
The delivery of neurofilaments via axonal transport has been proposed as an important mechanism for regulating axonal caliber. If this hypothesis is correct, alterations in axonal caliber should appear coincident with changes in the delivery of neurofilaments to the axon. The purpose of this study was to determine whether alterations in the caliber of axons in the proximal stumps of transected motor fibers precede, coincide with, or occur substantially later than changes in the delivery of neurofilaments via axonal transport. Between 3 d and 12 wk after crushing the sciatic nerves of 7-wk-old rats, lumbar motor neurons were labeled by the intraspinal injection of [35S]methionine. In neurons labeled between 3 d and 6 wk after axotomy, the relative amount of neurofilament protein in the slow component, as reflected by the ratio of the radioactivities of the 145-kD neurofilament protein to tubulin, was reduced to 30-40% of the control value. Moreover, as determined by immunoreactivity on blots, the amounts of neurofilament protein and tubulin in these nerve fibers were reduced fourfold and twofold, respectively. Thus, changes in the ratio of labeled neurofilament protein to tubulin correlated with comparable changes in the quantities of these proteins in nerve fibers. This decrease in the quantity of neurofilament proteins delivered to axons coincided temporally with reductions in axonal caliber. After regeneration occurred, the delivery of neurofilament proteins returned to pre-axotomy levels (i.e., 8 wk after axotomy), and caliber was restored with resumption of normal age-related radial growth of these axons. Thus, changes in axonal caliber coincided temporally with alterations in the delivery of neurofilament proteins. These results suggest that the majority of neurofilaments in these motor fibers continuously move in the anterograde direction as part of the slow component of axonal transport and that the transport of neurofilaments plays an important role in regulating the caliber of these axons.
通过轴突运输来传递神经丝被认为是调节轴突直径的一种重要机制。如果这一假说正确,那么轴突直径的改变应该与神经丝向轴突传递的变化同时出现。本研究的目的是确定横断运动纤维近端残端中轴突直径的改变是先于、与通过轴突运输传递神经丝的变化同时出现,还是在其之后才显著发生。在7周龄大鼠的坐骨神经被挤压后的3天至12周期间,通过脊髓内注射[35S]甲硫氨酸对腰段运动神经元进行标记。在轴突切断后3天至6周标记的神经元中,慢成分中神经丝蛋白的相对量,以145-kD神经丝蛋白与微管蛋白的放射性比值来反映,降至对照值的30 - 40%。此外,通过印迹免疫反应性测定,这些神经纤维中神经丝蛋白和微管蛋白的量分别减少了四倍和两倍。因此,标记的神经丝蛋白与微管蛋白的比值变化与神经纤维中这些蛋白质数量的类似变化相关。输送到轴突的神经丝蛋白数量的减少在时间上与轴突直径的减小同时出现。再生发生后,神经丝蛋白的输送恢复到轴突切断前的水平(即轴突切断后8周),并且随着这些轴突恢复与年龄相关的正常径向生长,直径得以恢复。因此,轴突直径的变化在时间上与神经丝蛋白输送的改变同时出现。这些结果表明,这些运动纤维中的大多数神经丝作为轴突运输慢成分的一部分持续向前运输,并且神经丝的运输在调节这些轴突的直径方面起着重要作用。