Teng H, Cole J C, Roberts R L, Wilkinson R S
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Neurosci. 1999 Jun 15;19(12):4855-66. doi: 10.1523/JNEUROSCI.19-12-04855.1999.
We have used a sensitive activity-dependent probe, sulforhodamine 101 (SR101), to view endocytic events within snake motor nerve terminals. After very brief neural stimulation at reduced temperature, SR101 is visualized exclusively at punctate sites located just inside the presynaptic membrane of each terminal bouton. The number of sites (approximately 26 sites/bouton) and their location (in register with postsynaptic folds) are similar to the number and location of active zones in snake motor terminals, suggesting a spatial association between exocytosis and endocytosis under these stimulus conditions. With more prolonged stimulation, larger SR101-containing structures appear at the bouton margins. Thus endocytosis occurs initially at distinct sites, which we call "endocytic active zones," whereas further stimulation recruits a second endocytic paradigm.
我们使用了一种灵敏的活性依赖型探针,磺基罗丹明101(SR101),来观察蛇运动神经末梢内的内吞事件。在低温下进行非常短暂的神经刺激后,SR101仅在每个终末小体突触前膜内侧的点状部位可见。这些部位的数量(每个小体约26个部位)及其位置(与突触后褶皱对齐)与蛇运动终末中活性区的数量和位置相似,这表明在这些刺激条件下,胞吐作用和内吞作用之间存在空间关联。随着刺激时间延长,终末小体边缘会出现更大的含SR101结构。因此,内吞作用最初发生在特定部位,我们称之为“内吞活性区”,而进一步刺激会引发第二种内吞模式。