Zhu Yongling, Xu Jian, Heinemann Stephen F
Molecular Neurobiology Laboratory, The Salk Institute, La Jolla, CA 92037, USA.
Commun Integr Biol. 2009 Sep;2(5):418-9. doi: 10.4161/cib.2.5.8896.
At nerve terminals, neurotransmitter release is mediated by exocytosis of synaptic vesicles at active zone. After exocytosis, vesicular components are efficiently retrieved by endocytosis. Tight coupling between synaptic vesicle exocytosis and endocytosis is critical for the maintenance of neurotransmission at central synapses. Recently, we have developed a new fluorescent pH reporter that permits us to examine exocytosis-endocytosis coupling at the level of individual synaptic vesicles at hippocampal synapses.1 To our surprise, we observed that the tight coupling of exocytosis and endocytosis broke down at very low stimulation frequencies, resulting in the generation of two endocytic vesicles per single exocytic fusion event. As stimulation frequency increased, exocytosis-endocytic coupling was restored with one endocytic vesicle generated for each vesicle exocytosed. Further studies revealed that the dissimilar patterns of exocytosis-endocytic coupling at different stimulation frequencies were mediated by two pathways of endocytosis that are orchestrated during differential patterns of neuronal activity.1 Here, we summarize our observations and further discuss their possible implications.
在神经末梢,神经递质的释放是由活跃区突触小泡的胞吐作用介导的。胞吐作用后,小泡成分通过内吞作用被有效地回收。突触小泡胞吐作用和内吞作用之间的紧密偶联对于维持中枢突触处的神经传递至关重要。最近,我们开发了一种新的荧光pH报告基因,使我们能够在海马突触的单个突触小泡水平上研究胞吐-内吞偶联。1令我们惊讶的是,我们观察到在非常低的刺激频率下,胞吐作用和内吞作用的紧密偶联被打破,导致每个单个胞吐融合事件产生两个内吞小泡。随着刺激频率的增加,胞吐-内吞偶联得以恢复,每个胞吐的小泡产生一个内吞小泡。进一步的研究表明,在不同刺激频率下胞吐-内吞偶联的不同模式是由两种内吞途径介导的,这两种途径在神经元活动的不同模式中被协调。1在这里,我们总结我们的观察结果,并进一步讨论它们可能的意义。