Edmonds B T, Koenig E
Department of Physiology, University at Buffalo, New York.
J Neurocytol. 1991 Mar;20(3):232-47. doi: 10.1007/BF01186996.
Growing retinal ganglion cell axons of the goldfish exhibit varicosities of varying sizes and smaller non-protruding phase-dense inclusions that are mobile and mediate rapid bulk redistribution of axoplasm. In fixed axons, Limax flavus agglutinin, a lectin specific for sialic acid which has been shown to inhibit organelle transport in these axons, preferentially labels surface membrane associated with varicosities and inclusions in preterminal axons. In viable axons, Limax flavus agglutinin causes: (1) agglutination of closely apposed axons, (2) redistribution of lectin-binding sites on varicosities to surfaces of interaxonal contact with other varicosities, forming 'fused' multivaricosity complexes, and (3) formation of vacuoles in many single varicosities and some multivaricosity complexes. Vacuoles contain Limax flavus agglutinin binding sites distributed circumferentially. On the basis of immunocytochemistry, actin, myosin, calmodulin and alpha-spectrin are co-localized with redistributed Limax flavus agglutinin binding sites. The agglutination, redistribution of lectin binding sites and changes in the cytoskeleton can be reversed by treatment with sialic acid. The lectin-induced vacuole formation and internalization of Limax flavus agglutinin receptors can also be blocked either by sodium azide in a glucose-free medium, or by pretreatment with cytochalasin D and indicate an energy and a cytoskeletal dependence. The Limax flavus agglutinin-induced structural rearrangements are not altered after limited digestion with pronase. Western blots after ultramicroelectrophoresis of retinal ganglion cell axons subjected to limited digestion reveal Limax flavus agglutinin labelling of bands with apparent Mr of 64 and 70 KDa. In undigested axons, some 70 KDa protein remains unextracted with Triton X-100 lysis of axonal fields, and more remains unextracted when axonal fields are pretreated with Limax flavus agglutinin before Triton lysis, suggesting increased association with the cytoskeleton in response to lectin binding. The results indicate that cross-linking of one or more sialoglycoconjugates on the surface of varicosities of preterminal growing retinal ganglion cell axons causes a constellation of transmembrane-mediated cytoskeletal and membrane changes that are akin to those described for capping in motile cells.
金鱼视网膜神经节细胞不断生长的轴突呈现出大小各异的膨体以及较小的、不突出的、相位密集的内含物,这些内含物可移动并介导轴浆的快速大量重新分布。在固定的轴突中,黄蛞蝓凝集素(一种对唾液酸具有特异性的凝集素,已被证明可抑制这些轴突中的细胞器运输)优先标记与膨体和终末前轴突中的内含物相关的表面膜。在有活力的轴突中,黄蛞蝓凝集素会导致:(1)紧密相邻的轴突发生凝集;(2)膨体上的凝集素结合位点重新分布到与其他膨体的轴突间接触表面,形成“融合”的多膨体复合体;(3)在许多单个膨体和一些多膨体复合体中形成液泡。液泡含有沿圆周分布的黄蛞蝓凝集素结合位点。基于免疫细胞化学,肌动蛋白、肌球蛋白、钙调蛋白和α - 血影蛋白与重新分布的黄蛞蝓凝集素结合位点共定位。凝集、凝集素结合位点的重新分布以及细胞骨架的变化可通过用唾液酸处理来逆转。凝集素诱导的液泡形成和黄蛞蝓凝集素受体的内化也可被无葡萄糖培养基中的叠氮化钠或用细胞松弛素D预处理所阻断,这表明其对能量和细胞骨架的依赖性。用链霉蛋白酶进行有限消化后,黄蛞蝓凝集素诱导的结构重排未发生改变。对经过有限消化的视网膜神经节细胞轴突进行超微电泳后的蛋白质免疫印迹显示,黄蛞蝓凝集素标记了表观分子量为64和70 kDa的条带。在未消化的轴突中,一些70 kDa的蛋白质在用Triton X - 100裂解轴突区域时仍未被提取出来,而当在Triton裂解前用黄蛞蝓凝集素预处理轴突区域时,更多的蛋白质未被提取出来,这表明响应凝集素结合,与细胞骨架的结合增加。结果表明,终末前生长的视网膜神经节细胞轴突膨体表面上一种或多种唾液酸糖缀合物的交联会引起一系列跨膜介导的细胞骨架和膜变化,这些变化类似于在运动细胞中描述的帽化现象。