Department of Cell and Developmental Biology, University of Michigan, Ann Arbor, Michigan 48109-2200, USA.
J Neurosci. 2011 Nov 30;31(48):17736-51. doi: 10.1523/JNEUROSCI.1482-11.2011.
The plt (pale tremor) mouse carries a null mutation in the Fig4(Sac3) gene that results in tremor, hypopigmentation, spongiform degeneration of the brain, and juvenile lethality. FIG4 is a ubiquitously expressed phosphatidylinositol 3,5-bisphosphate phosphatase that regulates intracellular vesicle trafficking along the endosomal-lysosomal pathway. In humans, the missense mutation FIG4(I41T) combined with a FIG4 null allele causes Charcot-Marie-Tooth 4J disease, a severe form of peripheral neuropathy. Here we show that Fig4 null mice exhibit a dramatic reduction of myelin in the brain and spinal cord. In the optic nerve, smaller-caliber axons lack myelin sheaths entirely, whereas many large- and intermediate-caliber axons are myelinated but show structural defects at nodes of Ranvier, leading to delayed propagation of action potentials. In the Fig4 null brain and optic nerve, oligodendrocyte (OL) progenitor cells are present at normal abundance and distribution, but the number of myelinating OLs is greatly compromised. The total number of axons in the Fig4 null optic nerve is not reduced. Developmental studies reveal incomplete myelination rather than elevated cell death in the OL linage. Strikingly, there is rescue of CNS myelination and tremor in transgenic mice with neuron-specific expression of Fig4, demonstrating a non-cell-autonomous function of Fig4 in OL maturation and myelin development. In transgenic mice with global overexpression of the human pathogenic FIG4 variant I41T, there is rescue of the myelination defect, suggesting that the CNS of CMT4J patients may be protected from myelin deficiency by expression of the FIG4(I41T) mutant protein.
plt(苍白震颤)小鼠携带 Fig4(Sac3)基因的无效突变,导致震颤、色素减退、脑海绵状变性和幼年致死。FIG4 是一种广泛表达的磷脂酰肌醇 3,5-二磷酸磷酸酶,可调节沿内体溶酶体途径的细胞内囊泡运输。在人类中,错义突变 FIG4(I41T)与 FIG4 无效等位基因的组合导致夏科-马里-图什 4J 病,这是一种严重的周围神经病。在这里,我们发现 Fig4 缺失小鼠表现出大脑和脊髓中髓鞘的明显减少。在视神经中,较小直径的轴突完全没有髓鞘,而许多大直径和中等直径的轴突有髓鞘,但在Ranvier 结处显示结构缺陷,导致动作电位的传播延迟。在 Fig4 缺失的大脑和视神经中,少突胶质细胞(OL)祖细胞的数量和分布正常,但髓鞘形成 OL 的数量大大减少。Fig4 缺失视神经中的轴突总数没有减少。发育研究表明,OL 谱系中存在不完全髓鞘形成而不是细胞死亡增加。引人注目的是,在神经元特异性表达 Fig4 的转基因小鼠中,中枢神经系统髓鞘形成和震颤得到挽救,表明 Fig4 在 OL 成熟和髓鞘发育中的非细胞自主功能。在过表达人类致病性 FIG4 变体 I41T 的转基因小鼠中,髓鞘缺陷得到挽救,这表明 CMT4J 患者的中枢神经系统可能通过表达 FIG4(I41T)突变蛋白而免受髓鞘缺乏的影响。