Watson D F, Glass J D, Griffin J W
Department of Neurology, Wayne State University School of Medicine, Detroit, Michigan 48201.
J Neurosci. 1993 Oct;13(10):4354-60. doi: 10.1523/JNEUROSCI.13-10-04354.1993.
Mice of the strain C57/BL/Ola exhibit a delay of Wallerian degeneration, such that axons survive for several weeks after a nerve transection that separates the axons from the cell bodies. In this Ola strain we have examined the distribution of cytoskeletal proteins in a 5 mm segment of the sciatic nerve for as long as 2 weeks after proximal and distal transections that prevent entry or exit of proteins via axonal transport. By 7 d after transections, there was a marked accumulation of alpha- and beta-tubulin, actin, and nonphosphorylated neurofilament epitopes at the proximal and at the distal ends of the transected axons, and loss of these proteins from the center of the isolated nerve segment. Highly phosphorylated neurofilament epitopes did not redistribute along the nerve, but there was a gradual loss of phosphorylated neurofilament immunoreactivity. These observations indicate the potential for bidirectional transport of a substantial portion of certain cytoskeletal proteins within axons of the PNS.
C57/BL/Ola品系的小鼠表现出华勒氏变性延迟,使得轴突在神经横断(将轴突与细胞体分离)后能存活数周。在这个Ola品系中,我们研究了坐骨神经5毫米节段中细胞骨架蛋白的分布,时间长达近端和远端横断后2周,这种横断可阻止蛋白质通过轴突运输进出。横断后7天,在横断轴突的近端和远端有α-和β-微管蛋白、肌动蛋白以及非磷酸化神经丝表位的明显积聚,而在分离神经节段的中部这些蛋白质缺失。高度磷酸化的神经丝表位未沿神经重新分布,但磷酸化神经丝免疫反应性逐渐丧失。这些观察结果表明,在周围神经系统的轴突内,相当一部分特定细胞骨架蛋白具有双向运输的潜力。