Garcia Michael L, Rao Mala V, Fujimoto Jiro, Garcia Virginia B, Shah Sameer B, Crum John, Gotow Takahiro, Uchiyama Yasuo, Ellisman Mark, Calcutt Nigel A, Cleveland Don W
Department of Biological Sciences, Bond Life Sciences Center, University of Missouri-Columbia, Columbia, Missouri 65211, USA.
J Neurosci. 2009 Feb 4;29(5):1277-84. doi: 10.1523/JNEUROSCI.3765-08.2009.
Neurofilament medium (NF-M) is essential for the acquisition of normal axonal caliber in response to a myelin-dependent "outside-in" trigger for radial axonal growth. Removal of the tail domain and lysine-serine-proline (KSP) repeats of NF-M, but not neurofilament heavy, produced axons with impaired radial growth and reduced conduction velocities. These earlier findings supported myelin-dependent phosphorylation of NF-M KSP repeats as an essential component of axonal growth. As a direct test of whether phosphorylation of NF-M KSP repeats is the target for the myelin-derived signal, gene replacement has now been used to produce mice in which all serines of NF-M's KSP repeats have been replaced with phosphorylation-incompetent alanines. This substitution did not alter accumulation of the neurofilaments or their subunits. Axonal caliber and motor neuron conduction velocity of mice expressing KSP phospho-incompetent NF-M were also indistinguishable from wild-type mice. Thus, phosphorylation of NF-M KSP repeats is not an essential component for the acquisition of normal axonal caliber mediated by myelin-dependent outside-in signaling.
神经丝蛋白中链(NF-M)对于响应髓磷脂依赖性的“由外向内”触发信号以实现正常轴突管径的获得至关重要,该信号用于径向轴突生长。去除NF-M的尾部结构域和赖氨酸-丝氨酸-脯氨酸(KSP)重复序列,但不去除神经丝蛋白重链,会导致轴突的径向生长受损且传导速度降低。这些早期发现支持了NF-M KSP重复序列的髓磷脂依赖性磷酸化是轴突生长的重要组成部分。作为对NF-M KSP重复序列磷酸化是否为髓磷脂衍生信号靶点的直接测试,现在已通过基因替代技术培育出小鼠,其中NF-M的KSP重复序列中的所有丝氨酸都被替换为无磷酸化能力的丙氨酸。这种替换并未改变神经丝蛋白及其亚基的积累。表达KSP磷酸化无能力的NF-M的小鼠的轴突管径和运动神经元传导速度与野生型小鼠也没有差异。因此,NF-M KSP重复序列的磷酸化并非髓磷脂依赖性由外向内信号传导介导的正常轴突管径获得的必要组成部分。