Teng H, Wilkinson R S
Department of Cell Biology and Physiology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Neurosci. 2000 Nov 1;20(21):7986-93. doi: 10.1523/JNEUROSCI.20-21-07986.2000.
We have used the activity-dependent probe FM1-43 with electron microscopy (EM) to examine endocytosis at the vertebrate nerve-muscle synapse. Preparations were fixed after very brief neural stimulation at reduced temperature, and internalized FM1-43 was photoconverted into an electron-dense reaction product. To locate the reaction product, we reconstructed computer renderings of individual terminal boutons from serial EM sections. Most of the reaction product was seen in 40-60 nm vesicles. All of the labeled vesicles were clathrin-coated, and 92% of them were located within 300 nm of the plasma membrane, suggesting that they had undergone little processing after retrieval from their endocytic sites. The vesicles (and by inference the sites) were not dispersed randomly near the plane of the membrane but instead were clustered significantly near active zones. Additional reaction product was found within putative macropinosomes; these appeared to form from deep membrane invaginations near active zones. Thus two mechanisms of endocytosis were evident after brief stimulation. Endocytosis near active zones is consistent with the existence of local exo/endocytic cycling pools. This mechanism also might serve to maintain alignment of active zones with postsynaptic folds during periods of activity when vesicular and plasma membranes are interchanged.
我们使用了依赖于活性的探针FM1-43结合电子显微镜(EM)来研究脊椎动物神经肌肉突触处的内吞作用。在低温下进行非常短暂的神经刺激后固定标本,内化的FM1-43被光转化为电子致密反应产物。为了定位反应产物,我们从连续的EM切片重建了单个终末小体的计算机渲染图。大部分反应产物见于40-60纳米的囊泡中。所有标记的囊泡都有网格蛋白包被,其中92%位于质膜300纳米范围内,这表明它们从内吞位点回收后几乎没有经过加工处理。这些囊泡(由此推断其位点)并非随机分散在膜平面附近,而是显著聚集在活性区附近。在假定的巨胞饮体中发现了额外的反应产物;这些似乎是由活性区附近的深膜内陷形成的。因此,短暂刺激后两种内吞机制很明显。活性区附近的内吞作用与局部外排/内吞循环池的存在一致。这种机制也可能有助于在囊泡膜和质膜相互交换的活动期间维持活性区与突触后褶皱的对齐。