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早期小儿多发性硬化症中神经胶质装置紊乱的意义。

Implication of perturbed axoglial apparatus in early pediatric multiple sclerosis.

机构信息

Department of Neurology and Neurosurgery, Montreal Neurological Institute and Hospital, McGill University and McGill University Health Centre, Quebec, Canada.

出版信息

Ann Neurol. 2012 May;71(5):601-13. doi: 10.1002/ana.22693. Epub 2012 Apr 4.

DOI:10.1002/ana.22693
PMID:22473675
Abstract

Cerebrospinal fluid samples collected from children during initial presentation of central nervous system inflammation, who may or may not subsequently be diagnosed as having multiple sclerosis (MS), were subjected to large-scale proteomics screening. Unexpectedly, major compact myelin membrane proteins typically implicated in MS were not detected. However, multiple molecules that localize to the node of Ranvier and the surrounding axoglial apparatus membrane were implicated, indicating perturbed axon-glial interactions in those children destined for diagnosis of MS.

摘要

从最初表现为中枢神经系统炎症且随后可能或不可能被诊断为多发性硬化症 (MS) 的儿童中收集的脑脊液样本,进行了大规模蛋白质组学筛选。出乎意料的是,通常与 MS 相关的主要紧凑髓鞘膜蛋白并未被检测到。然而,多个定位于Ranvier 结和周围轴突-胶质器细胞膜的分子被牵连在内,表明那些注定被诊断为 MS 的儿童的轴突-胶质相互作用受到了干扰。

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Implication of perturbed axoglial apparatus in early pediatric multiple sclerosis.早期小儿多发性硬化症中神经胶质装置紊乱的意义。
Ann Neurol. 2012 May;71(5):601-13. doi: 10.1002/ana.22693. Epub 2012 Apr 4.
2
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Activated microglia mediate axoglial disruption that contributes to axonal injury in multiple sclerosis.激活的小胶质细胞介导轴突胶质破坏,导致多发性硬化症中的轴突损伤。
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Neurodegeneration and humoral response proteins in cerebrospinal fluid associate with pediatric-onset multiple sclerosis and not monophasic demyelinating syndromes in childhood.脑脊液中的神经退行性变和体液反应蛋白与儿童发病的多发性硬化症有关,而与单相脱髓鞘综合征无关。
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