Department of Physiology & Neuroscience, New York University School of Medicine, New York, New York 10016, USA.
J Comp Neurol. 2010 Jul 15;518(14):2841-53. doi: 10.1002/cne.22367.
The consequences of dysmyelination are poorly understood and vary widely in severity. The shaking mouse, a quaking allele, is characterized by severe central nervous system (CNS) dysmyelination and demyelination, a conspicuous action tremor, and seizures in approximately 25% of animals, but with normal muscle strength and a normal lifespan. In this study we compare this mutant with other dysmyelinated mutants including the ceramide sulfotransferase deficient (CST-/-) mouse, which are more severely affected behaviorally, to determine what might underlie the differences between them with respect to behavior and longevity. Examination of the paranodal junctional region of CNS myelinated fibers shows that "transverse bands," a component of the junction, are present in nearly all shaking paranodes but in only a minority of CST-/- paranodes. The number of terminal loops that have transverse bands within a paranode and the number of transverse bands per unit length are only moderately reduced in the shaking mutant, compared with controls, but markedly reduced in CST-/- mice. Immunofluorescence studies also show that although the nodes of the shaking mutant are somewhat longer than normal, Na(+) and K(+) channels remain separated, distinguishing this mutant from CST-/- mice and others that lack transverse bands. We conclude that the essential difference between the shaking mutant and others more severely affected is the presence of transverse bands, which serve to stabilize paranodal structure over time as well as the organization of the axolemmal domains, and that differences in the prevalence of transverse bands underlie the marked differences in progressive neurological impairment and longevity among dysmyelinated mouse mutants.
少突胶质细胞发育不良的后果知之甚少,且严重程度差异很大。震颤鼠(shaking mouse)是一种震颤等位基因,其特征是严重的中枢神经系统(CNS)少突胶质细胞发育不良和脱髓鞘、明显的动作震颤以及大约 25%的动物出现癫痫发作,但肌肉力量正常且寿命正常。在这项研究中,我们将这种突变体与其他少突胶质细胞发育不良的突变体进行比较,包括半乳糖神经酰胺硫酸酯转移酶缺陷(CST-/-)小鼠,这些突变体在行为上受到更严重的影响,以确定它们在行为和寿命方面的差异可能有哪些基础。对 CNS 髓鞘纤维的连接部区域的检查表明,“横向带(transverse bands)”是连接部的一个组成部分,几乎存在于所有震颤的连接部,但只存在于少数 CST-/-连接部中。与对照组相比,在震颤突变体中,一个连接部内具有横向带的末端环数量和每单位长度的横向带数量仅适度减少,但在 CST-/-小鼠中则明显减少。免疫荧光研究还表明,尽管震颤突变体的节点比正常的稍长,但 Na(+)和 K(+)通道仍然分开,这将该突变体与 CST-/-小鼠和其他缺乏横向带的突变体区分开来。我们得出的结论是,震颤突变体与其他受影响更严重的突变体之间的根本区别在于存在横向带,这些带随着时间的推移有助于稳定连接部的结构以及轴膜域的组织,而横向带的出现频率差异是导致不同的少突胶质细胞发育不良小鼠突变体在进行性神经损伤和寿命方面存在显著差异的基础。