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Updated: Jan 11, 2026

Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons
07:30

Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons

Published on: September 4, 2017

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双Ca2+传感器在突触囊外细胞突变中的进化保守和分歧机制

Lei Li, Jingyao Xia, Jiafan Wang

    bioRxiv : the preprint server for biology
    |November 19, 2025
    PubMed
    概括

    这项研究揭示了两个传感器SNT-1和SNT-3是如何通过与SNARE复合体相互作用来控制C. elegans中神经递质释放的. 它们使用不同的快速和缓慢释放策略,SNT-1也调解自发释放.

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    Acute Dissociation of Lamprey Reticulospinal Axons to Enable Recording from the Release Face Membrane of Individual Functional Presynaptic Terminals12:01

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    Published on: October 1, 2014

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    Examination of Synaptic Vesicle Recycling Using FM Dyes During Evoked, Spontaneous, and Miniature Synaptic Activities08:10

    Examination of Synaptic Vesicle Recycling Using FM Dyes During Evoked, Spontaneous, and Miniature Synaptic Activities

    Published on: March 31, 2014

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    相关概念视频

    Fusion of Secretory Vesicles with the Plasma Membrane01:26

    Fusion of Secretory Vesicles with the Plasma Membrane

    Proteins and neurotransmitters in secretory vesicles can be released from a cell upon vesicle docking, priming, and fusion with the plasma membrane. Vesicles are docked and primed in preparation for the quick exocytosis of their contents in response to a stimulus. The fusion process is mainly carried out by a SNAP Receptor or SNARE complex, consisting of synaptobrevin, syntaxin-1, and SNAP-25.
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    Overview of Secretory Vesicles01:33

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    Exocytosis00:50

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