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脱髓鞘脊髓中移植嗅鞘细胞再髓鞘化后郎飞结的分子重建。

Molecular reconstruction of nodes of Ranvier after remyelination by transplanted olfactory ensheathing cells in the demyelinated spinal cord.

作者信息

Sasaki Masanori, Black Joel A, Lankford Karen L, Tokuno Hajime A, Waxman Stephen G, Kocsis Jeffery D

机构信息

Department of Neurology, Center for Neuroscience and Regeneration Research, Yale University School of Medicine, New Haven, Connecticut 06510, USA.

出版信息

J Neurosci. 2006 Feb 8;26(6):1803-12. doi: 10.1523/JNEUROSCI.3611-05.2006.

Abstract

Myelin-forming glial cells transplanted into the demyelinated spinal cord can form compact myelin and improve conduction properties. However, little is known of the expression and organization of voltage-gated ion channels in the remyelinated central axons or whether the exogenous cells provide appropriate signaling for the maturation of nodes of Ranvier. Here, we transplanted olfactory ensheathing cells from green fluorescent protein (GFP)-expressing donor rats [GFP-olfactory ensheathing cells (OECs)] into a region of spinal cord demyelination and found extensive remyelination, which included the development of mature nodal, paranodal, and juxtaparanodal domains, as assessed by ultrastructural, immunocytochemical, and electrophysiological analyses. In remyelinated axons, Nav1.6 was clustered at nodes, whereas Kv1.2 was aggregated in juxtaparanodal regions, recapitulating the distribution of these channels within mature nodes of uninjured axons. Moreover, the recruitment of Nav and Kv channels to specific membrane domains at remyelinated nodes persisted for at least 8 weeks after GFP-OEC transplantation. In vivo electrophysiological recordings demonstrated enhanced conduction along the GFP-OEC-remyelinated axons. These findings indicate that, in addition to forming myelin, engrafted GFP-OECs provide an environment that supports the development and maturation of nodes of Ranvier and the restoration of impulse conduction in central demyelinated axons.

摘要

移植到脱髓鞘脊髓中的形成髓鞘的胶质细胞能够形成紧密的髓鞘并改善传导特性。然而,对于再髓鞘化的中枢轴突中电压门控离子通道的表达和组织情况,或者外源性细胞是否为郎飞结的成熟提供适当的信号,我们知之甚少。在这里,我们将来自表达绿色荧光蛋白(GFP)的供体大鼠的嗅鞘细胞[GFP-嗅鞘细胞(OECs)]移植到脊髓脱髓鞘区域,发现了广泛的再髓鞘化,通过超微结构、免疫细胞化学和电生理分析评估,这包括成熟的结、旁结和近旁结区域的发育。在再髓鞘化的轴突中,Nav1.6聚集在结处,而Kv1.2聚集在近旁结区域,重现了这些通道在未损伤轴突成熟结内的分布。此外,在GFP-OEC移植后至少8周,Nav和Kv通道在再髓鞘化结处募集到特定膜结构域的现象持续存在。体内电生理记录表明,沿GFP-OEC再髓鞘化轴突的传导增强。这些发现表明,除了形成髓鞘外,植入的GFP-OECs还提供了一个支持郎飞结发育和成熟以及中枢脱髓鞘轴突冲动传导恢复的环境。

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