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日本患者脊髓多发性硬化症病变:施万细胞再髓鞘化发生在缺乏胶质纤维酸性蛋白(GFAP)的区域。

Spinal cord multiple sclerosis lesions in Japanese patients: Schwann cell remyelination occurs in areas that lack glial fibrillary acidic protein (GFAP).

作者信息

Itoyama Y, Ohnishi A, Tateishi J, Kuroiwa Y, Webster H D

出版信息

Acta Neuropathol. 1985;65(3-4):217-23. doi: 10.1007/BF00687001.

Abstract

To extend earlier observations on Schwann cell remyelination in multiple sclerosis (MS) lesions (Itoyama et al. 1983) we immunostained spinal cord sections from eight Japanese MS patients with antiserum to Po glycoprotein, a major constituent of peripheral nervous system (PNS) myelin, myelin basic protein (MBP), and glial fibrillary acidic protein (GFAP). Spinal cord sections from six of the eight Japanese MS patients contained large clusters of peripheral myelin sheaths with anti-Po immunoreactivity. In lesions found in four of the six patients, thousands of Po-stained PNS myelin sheaths were present. Necrosis was prominent in these lesions which included more than half of the spinal cord's transverse area. The number and density of regenerating myelin sheaths of peripheral origin were much greater than we observed in MS spinal cord lesions of white people (Itoyama et al. 1983). Anti-GFAP immunoreactivity was present in most brain and spinal cord lesions. However, the areas in lesions that contained large groups of PNS myelin sheaths lacked anti-GFAP immunoreactivity. Our data suggest that spinal MS lesions that are large, severely demyelinated, and partially necrotic may contain factors that inhibit fibrous astrogliosis. These factors, other substances in the large lesions and/or the lack of astrocytic scarring could then promote Schwann cell invasion, multiplication, and remyelination of surviving axons.

摘要

为扩展对多发性硬化症(MS)病灶中施万细胞再髓鞘化的早期观察结果(Itoyama等人,1983年),我们用针对外周神经系统(PNS)髓磷脂的主要成分Po糖蛋白、髓磷脂碱性蛋白(MBP)和胶质纤维酸性蛋白(GFAP)的抗血清,对8例日本MS患者的脊髓切片进行了免疫染色。8例日本MS患者中有6例的脊髓切片含有大量具有抗Po免疫反应性的外周髓鞘簇。在6例患者中的4例所发现的病灶中,存在数千个被Po染色的PNS髓鞘。这些病灶中的坏死很明显,其横截面积超过脊髓的一半。外周起源的再生髓鞘的数量和密度比我们在白人MS脊髓病灶中观察到的要大得多(Itoyama等人,1983年)。大多数脑和脊髓病灶中都存在抗GFAP免疫反应性。然而,含有大量PNS髓鞘的病灶区域缺乏抗GFAP免疫反应性。我们的数据表明,大的、严重脱髓鞘且部分坏死的脊髓MS病灶可能含有抑制纤维性星形胶质细胞增生的因子。这些因子、大病灶中的其他物质和/或星形细胞瘢痕形成的缺乏,可能会促进施万细胞的侵入、增殖以及对存活轴突的再髓鞘化。

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