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Role of transverse bands in maintaining paranodal structure and axolemmal domain organization in myelinated nerve fibers: effect on longevity in dysmyelinated mutant mice.横向带在维持有髓神经纤维的结旁结构和轴膜域组织中的作用:对脑白质营养不良突变小鼠寿命的影响。
J Comp Neurol. 2010 Jul 15;518(14):2841-53. doi: 10.1002/cne.22367.
2
Dysmyelination with preservation of transverse bands in a long-lived allele of the quaking mouse.在颤抖小鼠的一个长寿等位基因中,髓鞘形成异常但横带保留。
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3
Nodal sodium channel domain integrity depends on the conformation of the paranodal junction, not on the presence of transverse bands.结区钠通道结构域的完整性取决于旁结连接的构象,而非横向带的存在。
Glia. 2003 Feb;41(3):318-25. doi: 10.1002/glia.10179.
4
Paranodal dysmyelination in peripheral nerves of Trembler mice.震颤小鼠周围神经的连接部髓鞘异常。
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Freeze-fracture approaches to ionophore localization in normal and myelin-deficient nerves.用于正常和髓鞘缺乏神经中离子载体定位的冷冻断裂方法。
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6
Dependence of paranodal junctional gap width on transverse bands.结旁连接部间隙宽度对横行带的依赖性。
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Myelination of congenitally dysmyelinated spinal cord axons by adult neural precursor cells results in formation of nodes of Ranvier and improved axonal conduction.成年神经前体细胞对先天性脱髓鞘脊髓轴突进行髓鞘化,导致郎飞结形成并改善轴突传导。
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Spatiotemporal ablation of myelinating glia-specific neurofascin (Nfasc NF155) in mice reveals gradual loss of paranodal axoglial junctions and concomitant disorganization of axonal domains.在小鼠中对形成髓鞘的神经胶质特异性神经束蛋白(Nfasc NF155)进行时空消融,结果显示结旁轴突-神经胶质连接逐渐丧失,同时轴突结构域紊乱。
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Nodes of Ranvier act as barriers to restrict invasion of flanking paranodal domains in myelinated axons.郎飞结作为屏障,限制有髓轴突中侧翼结旁区域的入侵。
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Genetic dysmyelination alters the molecular architecture of the nodal region.遗传性髓鞘形成异常会改变结区的分子结构。
J Neurosci. 2002 Mar 1;22(5):1726-37. doi: 10.1523/JNEUROSCI.22-05-01726.2002.

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本文引用的文献

1
Multiple functions of the paranodal junction of myelinated nerve fibers.有髓神经纤维的结旁区的多种功能。
J Neurosci Res. 2009 Nov 15;87(15):3250-8. doi: 10.1002/jnr.22013.
2
Spatiotemporal ablation of myelinating glia-specific neurofascin (Nfasc NF155) in mice reveals gradual loss of paranodal axoglial junctions and concomitant disorganization of axonal domains.在小鼠中对形成髓鞘的神经胶质特异性神经束蛋白(Nfasc NF155)进行时空消融,结果显示结旁轴突-神经胶质连接逐渐丧失,同时轴突结构域紊乱。
J Neurosci Res. 2009 Jun;87(8):1773-93. doi: 10.1002/jnr.22015.
3
Maintenance of axo-oligodendroglial paranodal junctions requires DCC and netrin-1.轴突-少突胶质细胞结旁连接的维持需要DCC和netrin-1。
J Neurosci. 2008 Oct 22;28(43):11003-14. doi: 10.1523/JNEUROSCI.3285-08.2008.
4
Vesicular glutamate transporters define two sets of glutamatergic afferents to the somatosensory thalamus and two thalamocortical projections in the mouse.囊泡谷氨酸转运体定义了小鼠体感丘脑的两组谷氨酸能传入纤维以及两条丘脑皮质投射通路。
J Comp Neurol. 2008 Mar 10;507(2):1258-76. doi: 10.1002/cne.21592.
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Trafficking-dependent phosphorylation of Kv1.2 regulates voltage-gated potassium channel cell surface expression.Kv1.2依赖于运输的磷酸化调节电压门控钾通道的细胞表面表达。
Proc Natl Acad Sci U S A. 2007 Dec 11;104(50):20055-60. doi: 10.1073/pnas.0708574104. Epub 2007 Dec 3.
6
Gangliosides contribute to stability of paranodal junctions and ion channel clusters in myelinated nerve fibers.神经节苷脂有助于有髓神经纤维中结旁连接和离子通道簇的稳定性。
Glia. 2007 May;55(7):746-57. doi: 10.1002/glia.20503.
7
Immunohistochemical localization of CNTFRalpha in adult mouse retina and optic nerve following intraorbital nerve crush: evidence for the axonal loss of a trophic factor receptor after injury.眶内神经挤压后成年小鼠视网膜和视神经中CNTFRalpha的免疫组织化学定位:损伤后营养因子受体轴突损失的证据。
J Comp Neurol. 2007 Jan 10;500(2):384-400. doi: 10.1002/cne.21174.
8
Disruption of axo-glial junctions causes cytoskeletal disorganization and degeneration of Purkinje neuron axons.轴突-神经胶质连接的破坏会导致细胞骨架紊乱和浦肯野神经元轴突退化。
Proc Natl Acad Sci U S A. 2006 Mar 28;103(13):5137-42. doi: 10.1073/pnas.0601082103. Epub 2006 Mar 21.
9
Neurofascins are required to establish axonal domains for saltatory conduction.神经束蛋白是建立用于跳跃式传导的轴突区域所必需的。
Neuron. 2005 Dec 8;48(5):737-42. doi: 10.1016/j.neuron.2005.10.019.
10
Sulfatide is essential for the maintenance of CNS myelin and axon structure.硫脂对于中枢神经系统髓鞘和轴突结构的维持至关重要。
Glia. 2006 Mar;53(4):372-81. doi: 10.1002/glia.20292.

横向带在维持有髓神经纤维的结旁结构和轴膜域组织中的作用:对脑白质营养不良突变小鼠寿命的影响。

Role of transverse bands in maintaining paranodal structure and axolemmal domain organization in myelinated nerve fibers: effect on longevity in dysmyelinated mutant mice.

机构信息

Department of Physiology & Neuroscience, New York University School of Medicine, New York, New York 10016, USA.

出版信息

J Comp Neurol. 2010 Jul 15;518(14):2841-53. doi: 10.1002/cne.22367.

DOI:10.1002/cne.22367
PMID:20506478
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2879089/
Abstract

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.

摘要

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。