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中枢神经系统节点在有髓神经中的组装是由轴突细胞骨架促进的。

Assembly of CNS Nodes of Ranvier in Myelinated Nerves Is Promoted by the Axon Cytoskeleton.

机构信息

Centre for Neuroregeneration, University of Edinburgh, Edinburgh EH16 4SB, UK.

Centre de Recherche en Neurobiologie et Neurophysiologie de Marseille-UMR 7286, CNRS, 13344 Marseille, France.

出版信息

Curr Biol. 2017 Apr 3;27(7):1068-1073. doi: 10.1016/j.cub.2017.01.025. Epub 2017 Mar 16.

Abstract

Nodes of Ranvier in the axons of myelinated neurons are exemplars of the specialized cell surface domains typical of polarized cells. They are rich in voltage-gated sodium channels (Nav) and thus underpin rapid nerve impulse conduction in the vertebrate nervous system [1]. Although nodal proteins cluster in response to myelination, how myelin-forming glia influence nodal assembly is poorly understood. An axoglial adhesion complex comprising glial Neurofascin155 and axonal Caspr/Contactin flanks mature nodes [2]. We have shown that assembly of this adhesion complex at the extremities of migrating oligodendroglial processes promotes process convergence along the axon during central nervous system (CNS) node assembly [3]. Here we show that anchorage of this axoglial complex to the axon cytoskeleton is essential for efficient CNS node formation. When anchorage is disrupted, both the adaptor Protein 4.1B and the cytoskeleton protein βII spectrin are mislocalized in the axon, and assembly of the node of Ranvier is significantly delayed. Nodal proteins and migrating oligodendroglial processes are no longer juxtaposed, and single detached nodal complexes replace the symmetrical heminodes found in both the CNS and peripheral nervous system (PNS) during development. We propose that axoglial adhesion complexes contribute to the formation of an interface between cytoskeletal elements enriched in Protein 4.1B and βII spectrin and those enriched in nodal ankyrinG and βIV spectrin. This clusters nascent nodal complexes at heminodes and promotes their timely coalescence to form the mature node of Ranvier. These data demonstrate a role for the axon cytoskeleton in the assembly of a critical neuronal domain, the node of Ranvier.

摘要

有髓神经元轴突中的郎飞结是特化细胞表面结构域的典型范例,这些结构域存在于极化细胞中。郎飞结富含电压门控钠离子通道(Nav),因此是脊椎动物神经系统中快速神经冲动传导的基础[1]。尽管郎飞结蛋白在髓鞘形成后会聚集,但少突胶质细胞如何影响郎飞结的组装还知之甚少。由少突胶质细胞神经束蛋白 155(Neurofascin155)和轴突 Caspr/接触蛋白(Contactin)组成的轴-胶质黏附复合物侧翼成熟的郎飞结[2]。我们已经表明,在中枢神经系统(CNS)郎飞结组装过程中,该黏附复合物在迁移少突胶质细胞突起末端的组装促进了突起沿着轴突的汇聚[3]。在这里,我们表明该轴-胶质复合物与轴突细胞骨架的锚定对于有效的 CNS 郎飞结形成是必不可少的。当锚定被破坏时,衔接蛋白 4.1B 和细胞骨架蛋白 βII spectrin 都会在轴突中发生定位错误,郎飞结的组装会显著延迟。郎飞结蛋白和迁移的少突胶质细胞突起不再并列,并且单个分离的郎飞结复合物取代了在中枢神经系统和周围神经系统(PNS)发育过程中发现的对称半郎飞结。我们提出,轴-胶质黏附复合物有助于形成富含衔接蛋白 4.1B 和 βII spectrin 的细胞骨架元件与富含郎飞结锚蛋白 G 和 βIV spectrin 的细胞骨架元件之间的界面。这将新生的郎飞结复合物聚集在半郎飞结上,并促进它们的及时融合以形成成熟的郎飞结。这些数据表明轴突细胞骨架在郎飞结这一关键神经元结构域的组装中发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d5a1/5387178/1100615ab939/gr1.jpg

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