Cooper B J, Duncan I, Cummings J, de Lahunta A
Acta Neuropathol. 1984;63(1):51-6. doi: 10.1007/BF00688470.
Segments of peripheral nerve from dogs with canine inherited hypertrophic neuropathy ( CIHN ) were transplanted to the transected sciatic nerve of immuno incompetent mice. Regenerating mouse axons penetrated the grafts and were myelinated by dog Schwann cells. In grafts collected 3 or more months after transplantation, filamentous or granular material, identical to that occurring in nerves of affected dogs, accumulated in myelinating Schwann cells. Demyelinated fibers were only rarely found in grafted segments of affected nerve. Neither filamentous accumulations nor demyelination were observed in grafts of control canine nerve. These results indicate that CIHN is associated with a defect in Schwann cell function, and the abnormal accumulations of filaments suggest that the defect may be in the cytoskeleton. The rarity of demyelination in grafts suggests that some factor in addition to the Schwann cell defect is required to precipitate myelin destruction.
将患有犬遗传性肥厚性神经病(CIHN)的犬的外周神经段移植到免疫功能低下小鼠的坐骨神经切断处。再生的小鼠轴突穿透移植物,并由犬雪旺细胞髓鞘化。在移植后3个月或更长时间收集的移植物中,与患病犬神经中出现的丝状或颗粒状物质相同的物质积聚在髓鞘形成的雪旺细胞中。在受影响神经的移植段中很少发现脱髓鞘纤维。在对照犬神经移植物中未观察到丝状积聚和脱髓鞘现象。这些结果表明,CIHN与雪旺细胞功能缺陷有关,细丝的异常积聚表明缺陷可能存在于细胞骨架中。移植物中脱髓鞘现象的罕见性表明,除了雪旺细胞缺陷外,还需要一些其他因素才能引发髓鞘破坏。