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本文引用的文献

1
Postnatal Loss of Neuronal and Glial Neurofascins Differentially Affects Node of Ranvier Maintenance and Myelinated Axon Function.出生后神经元和胶质神经束蛋白的缺失对郎飞结的维持和有髓轴突功能有不同影响。
Front Cell Neurosci. 2017 Feb 3;11:11. doi: 10.3389/fncel.2017.00011. eCollection 2017.
2
Early and Late Loss of the Cytoskeletal Scaffolding Protein, Ankyrin G Reveals Its Role in Maturation and Maintenance of Nodes of Ranvier in Myelinated Axons.细胞骨架支架蛋白锚蛋白G的早期和晚期缺失揭示了其在有髓轴突郎飞结成熟和维持中的作用。
J Neurosci. 2017 Mar 8;37(10):2524-2538. doi: 10.1523/JNEUROSCI.2661-16.2017. Epub 2017 Feb 1.
3
Neurexin, Neuroligin and Wishful Thinking coordinate synaptic cytoarchitecture and growth at neuromuscular junctions.神经连接蛋白、神经配蛋白和如意算盘蛋白协同调节神经肌肉接头处的突触细胞结构和生长。
Mol Cell Neurosci. 2017 Jan;78:9-24. doi: 10.1016/j.mcn.2016.11.004. Epub 2016 Nov 10.
4
Auto-antibodies to contactin-associated protein 1 (Caspr) in two patients with painful inflammatory neuropathy.两名患有疼痛性炎性神经病患者体内针对接触蛋白相关蛋白1(Caspr)的自身抗体。
Brain. 2016 Oct;139(Pt 10):2617-2630. doi: 10.1093/brain/aww189. Epub 2016 Jul 29.
5
Synaptic Deficits at Neuromuscular Junctions in Two Mouse Models of Charcot-Marie-Tooth Type 2d.夏科-马里-图斯病2D型两种小鼠模型中神经肌肉接头处的突触缺陷
J Neurosci. 2016 Mar 16;36(11):3254-67. doi: 10.1523/JNEUROSCI.1762-15.2016.
6
Lack of motor recovery after prolonged denervation of the neuromuscular junction is not due to regenerative failure.神经肌肉接头长期去神经支配后运动功能未恢复并非由于再生失败。
Eur J Neurosci. 2016 Feb;43(3):451-62. doi: 10.1111/ejn.13059. Epub 2015 Sep 28.
7
Mechanisms Regulating Neuromuscular Junction Development and Function and Causes of Muscle Wasting.调控神经肌肉接头发育和功能的机制以及肌肉萎缩的原因。
Physiol Rev. 2015 Jul;95(3):809-52. doi: 10.1152/physrev.00033.2014.
8
Synaptic abnormalities and cytoplasmic glutamate receptor aggregates in contactin associated protein-like 2/Caspr2 knockout neurons.接触蛋白相关蛋白样2/接触蛋白相关蛋白2(Caspr2)基因敲除神经元中的突触异常和细胞质谷氨酸受体聚集体
Proc Natl Acad Sci U S A. 2015 May 12;112(19):6176-81. doi: 10.1073/pnas.1423205112. Epub 2015 Apr 27.
9
Caspr and caspr2 are required for both radial and longitudinal organization of myelinated axons.髓鞘化轴突的径向和纵向组织都需要接触蛋白相关蛋白(Caspr)和接触蛋白相关蛋白2(Caspr2)。
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10
Loss of glial neurofascin155 delays developmental synapse elimination at the neuromuscular junction.神经胶质细胞神经束蛋白 155 的缺失会延迟神经肌肉接头处发育性突触消除。
J Neurosci. 2014 Sep 17;34(38):12904-18. doi: 10.1523/JNEUROSCI.1725-14.2014.

Caspr1和Caspr2突变的有髓轴突中的轴突结构域紊乱会影响神经肌肉接头的完整性,导致肌肉萎缩。

Axonal domain disorganization in Caspr1 and Caspr2 mutant myelinated axons affects neuromuscular junction integrity, leading to muscle atrophy.

作者信息

Saifetiarova Julia, Liu Xi, Taylor Anna M, Li Jie, Bhat Manzoor A

机构信息

Department of Cellular and Integrative Physiology, Center for Biomedical Neuroscience, School of Medicine, University of Texas Health Science Center, San Antonio, Texas.

Xiangya School of Medicine, Central South University, Changsha, China.

出版信息

J Neurosci Res. 2017 Jul;95(7):1373-1390. doi: 10.1002/jnr.24052. Epub 2017 Apr 3.

DOI:10.1002/jnr.24052
PMID:28370195
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5435537/
Abstract

Bidirectional interactions between neurons and myelinating glial cells result in formation of axonal domains along myelinated fibers. Loss of axonal domains leads to detrimental consequences on nerve structure and function, resulting in reduced conductive properties and the diminished ability to reliably transmit signals to the targets they innervate. Thus, impairment of peripheral myelinated axons that project to the surface of muscle fibers and form neuromuscular junction (NMJ) synapses leads to muscle dysfunction. The goal of our studies was to determine how altered electrophysiological properties due to axonal domain disorganization lead to muscle pathology, which is relevant to a variety of peripheral neuropathies, demyelinating diseases, and neurodegenerative disorders. Using conventional Contactin-Associated Protein 1 (Caspr1) and Caspr2 single or double mutants with disrupted paranodal, juxtaparanodal, or both regions, respectively, in peripheral myelinated axons, we correlated defects in NMJ integrity and muscle pathology. Our data show that loss of axonal domains in Caspr1 and Caspr2 single and double mutants primarily alters distal myelinated fibers together with presynaptic terminals, eventually leading to NMJ denervation and reduction in postsynaptic endplate areas. Moreover, reduction in conductive properties of peripheral myelinated fibers together with NMJ disintegration leads to muscle atrophy in Caspr1 mutants or muscle fiber degeneration accompanied by mitochondrial dysfunction in Caspr1/Caspr2 double mutants. Together, our data indicate that proper organization of axonal domains in myelinated fibers is critical for optimal propagation of electrical signals, NMJ integrity, and muscle health, and provide insights into a wide range of pathologies that result in reduced nerve conduction leading to muscle atrophy. © 2017 Wiley Periodicals, Inc.

摘要

神经元与髓鞘形成性神经胶质细胞之间的双向相互作用导致沿有髓纤维形成轴突结构域。轴突结构域的丧失会对神经结构和功能产生有害影响,导致传导特性降低以及向其支配的靶标可靠传递信号的能力减弱。因此,投射到肌纤维表面并形成神经肌肉接头(NMJ)突触的外周有髓轴突受损会导致肌肉功能障碍。我们研究的目的是确定由于轴突结构域紊乱导致的电生理特性改变如何导致肌肉病变,这与多种周围神经病、脱髓鞘疾病和神经退行性疾病相关。利用外周有髓轴突中分别破坏了旁结、近旁结或两者区域的传统接触蛋白相关蛋白1(Caspr1)和Caspr2单突变体或双突变体,我们将NMJ完整性缺陷与肌肉病变联系起来。我们的数据表明,Caspr1和Caspr2单突变体及双突变体中轴突结构域的丧失主要改变了远端有髓纤维以及突触前终末,最终导致NMJ失神经支配和突触后终板面积减小。此外,外周有髓纤维传导特性的降低以及NMJ解体导致Caspr1突变体出现肌肉萎缩,或Caspr1/Caspr2双突变体出现伴有线粒体功能障碍的肌纤维变性。总之,我们的数据表明,有髓纤维中轴突结构域的正确组织对于电信号的最佳传播、NMJ完整性和肌肉健康至关重要,并为导致神经传导降低进而导致肌肉萎缩的多种病理状况提供了见解。© 2017威利期刊公司