Hall S, Berry M
Anatomy Department, United Medical School of Guy's Hospital, London, UK.
J Neurocytol. 1989 Apr;18(2):171-84. doi: 10.1007/BF01206660.
The interactions between retinal ganglion cell (RGC) axons and glia at the site of optic nerve section and at the junctional zone between optic nerve and cellular or acellular peripheral nerve (PN) grafts have been studied electron microscopically. After transection, RGC axons, accompanied by processes of astrocyte cytoplasm, grew out from the proximal optic nerve stump into the scar tissue that developed between proximal and distal stumps. However, axons failed to cross the scar, and none entered the distal stump. By 3 days post lesion (DPL), bundles of RGC axons, accompanied by astrocytes and oligodendrocytes, grew out from the proximal optic nerve stump into the junctional zone between optic nerve and either type of PN graft. The bundles of RGC axons and growth cones that grew towards acellular PN grafts degenerated within 10-20 DPL; by 30 DPL a small number of axons persisted within the end of the proximal optic nerve stump. No axons were seen within the acellular PN grafts. These results suggest that reactive axonal sprouting, axon outgrowth and glial migration from the proximal optic nerve stump are events that occur during an acute response to injury, and that they are independent of the presence of Schwann cells. However, it would appear that few axons entered either scar or junctional zone unless accompanied by glia. There was little evidence that axon outgrowth was laminin-dependent. The bundles that grew towards cellular PN grafts encountered cells that we have identified as Schwann cells within the junctional zone: the axons in these bundles survived and entered the cellular grafts. Schwann cells migrated into the junctional zone from the cellular PN graft. It is probable that Schwann cells facilitated RGC axon entry into the graft directly by both cell contact and the secretion of neuronotrophic factors, and indirectly by modifying the CNS glia in the junctional zone.
我们已经通过电子显微镜研究了视网膜神经节细胞(RGC)轴突与视神经切断部位以及视神经与细胞性或无细胞性周围神经(PN)移植物交界处的神经胶质之间的相互作用。切断后,RGC轴突伴随着星形胶质细胞胞质突起,从视神经近端残端长入近端和远端残端之间形成的瘢痕组织中。然而,轴突未能穿过瘢痕,也没有进入远端残端。损伤后3天(DPL),RGC轴突束伴随着星形胶质细胞和少突胶质细胞,从视神经近端残端长入视神经与任何一种PN移植物之间的交界区。向无细胞PN移植物生长的RGC轴突束和生长锥在10 - 20 DPL内退化;到30 DPL时,少数轴突仍存在于视神经近端残端末端。在无细胞PN移植物中未见轴突。这些结果表明,反应性轴突发芽、轴突生长以及从视神经近端残端的神经胶质迁移是损伤急性反应期间发生的事件,并且它们独立于施万细胞的存在。然而,除非有神经胶质伴随,似乎很少有轴突进入瘢痕或交界区。几乎没有证据表明轴突生长依赖层粘连蛋白。向细胞性PN移植物生长的束在交界区内遇到了我们鉴定为施万细胞的细胞:这些束中的轴突存活并进入了细胞性移植物。施万细胞从细胞性PN移植物迁移到交界区。施万细胞可能通过细胞接触和神经营养因子的分泌直接促进RGC轴突进入移植物,并通过改变交界区的中枢神经系统神经胶质间接促进。