Berry M, Hall S, Follows R, Wyse J P
Department of Anatomy, United Medical School of Guy's Hospital, London, UK.
J Neurocytol. 1989 Apr;18(2):141-59. doi: 10.1007/BF01206658.
The Browman-Wyse (BW) rat displays a spectrum of ocular abnormalities which include myelination by Schwann cells of retinal ganglion cell (RGC) axons within the retina. Immunohistochemical and ultrastructural studies of the optic nerves of adult BW rats (30-60 days of age) with myelinated intraretinal axons were performed. Although individual nerves displayed considerable morphological variability, all were characterized by an initial dysmyelinated proximal segment which was separated from a normally myelinated distal segment by a transitional junctional zone. The proximal segment contained axons which were predominantly unmyelinated: where myelination occurred, almost all sheaths were Po-positive, proteolipid protein-negative, and the myelinating cell was a Schwann cell. In the distal segment the distribution of myelinated axons appeared to be normal, sheaths were PLP+, and the myelinating cell was an oligodendrocyte. Within the proximal segment, axons that were myelinated by Schwann cells were isolated by a basal lamina and expanded extracellular spaces from the bulk of other RGC axons within the optic nerve. Few carbonic anhydrase (CAII)+ or GalC+ oligodendrocytes were seen in proximal segments that contained Schwann cells: anti-CAII antibody stained atypical cells within the proximal segments which did not resemble CAII+ oligodendrocytes in the distal segment, and which were probably GalC-. Astrocytes appeared normal throughout the length of the nerve, and there was no morphological specialization at the junctional zone similar to that at the lamina cribrosa. The possible source(s) of the intraneural Schwann cells, and the pathogenetic mechanisms underlying the aberrant myelination of RGC axons within the BW optic nerve are discussed.
布朗曼-怀斯(BW)大鼠表现出一系列眼部异常,其中包括视网膜内视网膜神经节细胞(RGC)轴突被施万细胞髓鞘化。对成年BW大鼠(30 - 60日龄)视网膜内有髓鞘轴突的视神经进行了免疫组织化学和超微结构研究。尽管各条神经在形态上有很大差异,但所有神经的特征都是起始段近端髓鞘形成异常,该段与正常髓鞘化的远端段之间有一个过渡连接区。近端段包含的轴突主要是无髓鞘的:在发生髓鞘化的地方,几乎所有的髓鞘都是Po阳性、蛋白脂蛋白阴性,且髓鞘形成细胞是施万细胞。在远端段,有髓鞘轴突的分布似乎正常,髓鞘是PLP阳性,髓鞘形成细胞是少突胶质细胞。在近端段,被施万细胞髓鞘化的轴突被基膜和扩大的细胞外间隙与视神经内的其他大部分RGC轴突隔离开来。在含有施万细胞的近端段,很少见到碳酸酐酶(CAII)阳性或半乳糖脑苷脂(GalC)阳性的少突胶质细胞:抗CAII抗体在近端段内染色的非典型细胞与远端段的CAII阳性少突胶质细胞不同,可能是GalC阴性。在整个神经长度上,星形胶质细胞看起来正常,连接区没有类似于筛板处的形态特化。文中讨论了神经内施万细胞的可能来源以及BW视神经内RGC轴突异常髓鞘化的发病机制。