Ko C P, Propst J W
J Neurocytol. 1986 Apr;15(2):231-40. doi: 10.1007/BF01611659.
Freeze-fracture combined with filipin treatment has been used as a cytochemical probe for membrane cholesterol. As previously shown at the frog neuromuscular junction, distinctive sterol-specific complexes were formed on the presynaptic membrane after filipin treatment, except at active zones. The absence of sterol-specific complexes from active zones was confirmed using two other cytochemical agents--digitonin and saponin. We also studied the maintenance and differentiation of the presynaptic membrane heterogeneity revealed by membrane cholesterol probes at degenerating and regenerating neuromuscular junctions. During degeneration, active zones in frog nerve terminals were disorganized, but still lacked sterol-specific complexes. After engulfing the degenerating nerve terminals, Schwann cells occupied the synaptic gutters and displayed a uniform distribution of sterol-specific complexes. Schwann cell ridges opposite the postjunctional folds also had prominent sterol-specific complexes in regions formerly occupied by active zones. By 2 weeks after nerve crush, nerve terminals reinvaded the endplate region and active zones began to regenerate. While the intramembrane particles of the early regenerating active zones were not arranged in the normal double-rowed organization, filipin-sterol complexes were nevertheless excluded from these primitive active zones. Areas of nerve terminal membrane opposite to junctional folds but lacking active zones were covered with filipin-sterol complexes. These results show that the normal double-rowed organization is not required for the expression of the membrane heterogeneity associated with the active zone. In addition, the absence of sterol-specific complexes is closely associated with the active zone particles and not simply the membrane regions opposite to the postjunctional folds. The membrane heterogeneity does not seem to be directly linked with the functional state of the active zone since it is still associated with degenerating active zones after transmission failure has occurred.
冷冻蚀刻结合制霉菌素处理已被用作膜胆固醇的细胞化学探针。如先前在青蛙神经肌肉接头处所示,制霉菌素处理后,除了活性区外,突触前膜上形成了独特的甾醇特异性复合物。使用另外两种细胞化学试剂——洋地黄皂苷和皂角苷,证实了活性区不存在甾醇特异性复合物。我们还研究了在退化和再生的神经肌肉接头处,膜胆固醇探针所揭示的突触前膜异质性的维持和分化。在退化过程中,青蛙神经末梢的活性区紊乱,但仍缺乏甾醇特异性复合物。雪旺细胞吞噬退化的神经末梢后,占据了突触沟,并显示出甾醇特异性复合物的均匀分布。与接头后褶皱相对的雪旺细胞嵴在先前被活性区占据的区域也有突出的甾醇特异性复合物。神经挤压后2周,神经末梢重新侵入终板区域,活性区开始再生。虽然早期再生活性区的膜内颗粒没有排列成正常的双排结构,但制霉菌素-甾醇复合物仍被排除在这些原始活性区之外。与接头褶皱相对但缺乏活性区的神经末梢膜区域覆盖着制霉菌素-甾醇复合物。这些结果表明,与活性区相关的膜异质性表达不需要正常的双排结构。此外,甾醇特异性复合物的缺失与活性区颗粒密切相关,而不仅仅是与接头后褶皱相对的膜区域。膜异质性似乎与活性区的功能状态没有直接联系,因为在传递失败后,它仍然与退化的活性区相关。