Griffiths I R, McCulloch M C, Abrahams S
J Neurocytol. 1987 Apr;16(2):145-53. doi: 10.1007/BF01795299.
Changes in the myelin sheath have been studied in the nerve roots of dogs with Progressive axonopathy, an autosomal recessive inherited neuropathy. The earliest changes were attenuation of the sheath at the proximal paranode and adjacent internode, probably in response to the axonal swelling which occurs in this area. Myelin bubbles were frequently observed along internodes. As the disease developed, progressively more fibres demonstrated short internodes of irregular length and thin myelin sheaths suggesting extensive remyelination and remodelling of the sheath. Short lengths of axons devoid of myelin, and occasional macrophages were also encountered. Sheaths of both original and newly formed internodes were highly irregular in outline. Occasional intra-axonal projections of adaxonal Schwann cell cytoplasm were observed, but complex interdigitations were unusual. A moderately electron-dense, granular material accumulated within the myelin sheath, becoming more obvious in the advanced disease. This material of unknown origin and composition was located predominantly at the intraperiod line principally between the adaxonal cytoplasm and the inner major dense line, but also at Schmidt-Lanterman incisures and between paranodal loops. Xenografts of the canine nerves into athymic mice failed to demonstrate any of the myelin sheath changes. The temporal and spatial relationship of the myelin sheath and axonal changes and the failure to reproduce the natural lesion in grafts suggest that Schwann cell alterations probably occur in response to the axonal changes.
在患有进行性轴索性神经病(一种常染色体隐性遗传性神经病)的犬类神经根中,对髓鞘变化进行了研究。最早的变化是近端结旁和相邻结间的髓鞘变薄,这可能是对该区域发生的轴突肿胀的反应。沿结间经常观察到髓鞘泡。随着疾病发展,越来越多的纤维表现出长度不规则的短结间和薄髓鞘,提示广泛的髓鞘再生和鞘重塑。还遇到了短段无髓鞘的轴突和偶尔的巨噬细胞。原始和新形成结间的鞘轮廓高度不规则。观察到偶尔有轴突旁施万细胞胞质的轴突内突起,但复杂的指状交叉不常见。一种中等电子密度的颗粒物质在髓鞘内积聚,在疾病晚期变得更加明显。这种来源和成分不明的物质主要位于轴突旁细胞质和内侧主要致密线之间的周期线内,但也存在于施密特-兰特尔曼切迹和结旁环之间。将犬神经异种移植到无胸腺小鼠中未显示出任何髓鞘变化。髓鞘和轴突变化的时间和空间关系以及在移植中未能重现自然病变表明,施万细胞改变可能是对轴突变化的反应。