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颤搐小鼠的周围神经病变:神经内膜中细胞外基质的积累及离子通道的异常表达。

Peripheral neuropathy in the twitcher mouse: accumulation of extracellular matrix in the endoneurium and aberrant expression of ion channels.

作者信息

Kagitani-Shimono Kuriko, Mohri Ikuko, Yagi Takashi, Taniike Masako, Suzuki Kinuko

机构信息

Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.

出版信息

Acta Neuropathol. 2008 May;115(5):577-87. doi: 10.1007/s00401-007-0333-3. Epub 2008 Jan 3.

Abstract

Globoid cell leukodystrophy (GLD; Krabbe's disease), caused by a genetic galactosylceramidase deficiency, affects both the central and peripheral nervous systems (CNS and PNS). Allogenic hematopoietic stem-cell transplantation (HSCT) has been beneficial for clinical improvement of this disease. However, recent reports by Siddiqi et al. suggested that none of their transplanted patients achieved complete normalization of their peripheral nerve function, despite the well-documented remyelination of the CNS and PNS in the treated patients. We hypothesized that the PNS dysfunction in GLD is due to altered Schwann cell-axon interactions, resulting in structural abnormalities of the node of Ranvier and aberrant expression of ion channels caused by demyelination and that the persistence of this altered interaction is responsible for the dysfunction of the PNS after HSCT. Since there has not been any investigation of the Schwann cell-axonal relationship in twitcher mice, an authentic model of GLD, we first investigated structural abnormalities, focusing on the node of Ranvier in untreated twitcher mice, and compared the results with those obtained after receiving bone marrow transplantation (BMT). As expected, we found numerous supernumerary Schwann cells that formed structurally abnormal nodes of Ranvier. Similar findings, though at somewhat variable extent, were detected in mice treated with BMT. Activated supernumerary Schwann cells expressed GFAP immunoreactivity and generated Alcian blue-positive extracellular matrix (ECM) in the endoneurial space. The processes of these supernumerary Schwann cells often covered and obliterated the nodal regions. Furthermore, the distribution of Na(+) channel immunoreactivity was diffuse without the concentration at the nodes of Ranvier as seen in wild-type mice. Neither K(+) channels nor Neurexin IV/ Caspr/ Paranoidin (NCP-1) were detected in the twi/twi sciatic nerve. The results of our study suggest the importance of normalization of the Schwann cell-axon relationship for the functional recovery of peripheral nerves, when one considers therapeutic strategies for PNS pathology in GLD.

摘要

球状细胞脑白质营养不良(GLD;克拉伯病)由遗传性半乳糖神经酰胺酶缺乏引起,会影响中枢神经系统和周围神经系统(CNS和PNS)。同种异体造血干细胞移植(HSCT)对该疾病的临床改善有益。然而,西迪基等人最近的报告表明,尽管在接受治疗的患者中,CNS和PNS有充分记录的髓鞘再生,但他们移植的患者中没有一人实现外周神经功能的完全正常化。我们推测,GLD中的PNS功能障碍是由于雪旺细胞 - 轴突相互作用改变,导致郎飞结结构异常以及脱髓鞘引起的离子通道异常表达,并且这种改变的相互作用持续存在是HSCT后PNS功能障碍的原因。由于尚未对GLD的真实模型——抽搐小鼠的雪旺细胞 - 轴突关系进行任何研究,我们首先研究了未经治疗的抽搐小鼠郎飞结的结构异常,并将结果与接受骨髓移植(BMT)后的结果进行比较。不出所料,我们发现大量多余的雪旺细胞形成了结构异常的郎飞结。在接受BMT治疗的小鼠中也检测到了类似的结果,尽管程度有所不同。活化的多余雪旺细胞表达GFAP免疫反应性,并在内神经间隙产生阿尔辛蓝阳性细胞外基质(ECM)。这些多余雪旺细胞的突起常常覆盖并遮挡了结区。此外,与野生型小鼠不同,Na(+)通道免疫反应性的分布是弥散的,没有集中在郎飞结处。在twi/twi坐骨神经中未检测到K(+)通道或神经连接蛋白IV/接触蛋白相关蛋白/ paranodin(NCP - 1)。我们的研究结果表明,在考虑GLD中PNS病理学的治疗策略时,雪旺细胞 - 轴突关系的正常化对于外周神经功能恢复的重要性。

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