Synaptic Vesicle Endocytosis in Different Model Systems.
Synaptic Vesicle Endocytosis in Different Model Systems.
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DOI:
10.3389/fncel.2018.00171
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发表时间:
2018
影响因子:
5.3
通讯作者:
Watanabe S
中科院分区:
文献类型:
--
作者:
Gan Q;Watanabe S
Neurotransmission in complex animals depends on a choir of functionally distinct synapses releasing neurotransmitters in a highly coordinated manner. During synaptic signaling, vesicles fuse with the plasma membrane to release their contents. The rate of vesicle fusion is high and can exceed the rate at which synaptic vesicles can be re-supplied by distant sources. Thus, local compensatory endocytosis is needed to replenish the synaptic vesicle pools. Over the last four decades, various experimental methods and model systems have been used to study the cellular and molecular mechanisms underlying synaptic vesicle cycle. Clathrin-mediated endocytosis is thought to be the predominant mechanism for synaptic vesicle recycling. However, recent studies suggest significant contribution from other modes of endocytosis, including fast compensatory endocytosis, activity-dependent bulk endocytosis, ultrafast endocytosis, as well as kiss-and-run. Currently, it is not clear whether a universal model of vesicle recycling exist for all types of synapses. It is possible that each synapse type employs a particular mode of endocytosis. Alternatively, multiple modes of endocytosis operate at the same synapse, and the synapse toggles between different modes depending on its activity level. Here we compile review and research articles based on well-characterized model systems: frog neuromuscular junctions, C. elegans neuromuscular junctions, Drosophila neuromuscular junctions, lamprey reticulospinal giant axons, goldfish retinal ribbon synapses, the calyx of Held, and rodent hippocampal synapses. We will compare these systems in terms of their known modes and kinetics of synaptic vesicle endocytosis, as well as the underlying molecular machineries. We will also provide the future development of this field.
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DOI:
10.1083/jcb.57.2.499
发表时间:
1973-05
期刊:
The Journal of cell biology
影响因子:
--
作者:
Ceccarelli B;Hurlbut WP;Mauro A
通讯作者:
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影响因子:
16.6
作者:
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影响因子:
5.5
作者:
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通讯作者:
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影响因子:
56.9
作者:
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通讯作者:
BEWICK, GS
DOI:
10.1073/pnas.0707574105
发表时间:
2007-12-18
影响因子:
11.1
作者:
Balaji, J.;Ryan, T. A.
通讯作者:
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