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Fusion of Secretory Vesicles with the Plasma Membrane01:26

Fusion of Secretory Vesicles with the Plasma Membrane

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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.
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
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Exocytosis00:50

Exocytosis

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Exocytosis is a process that releases molecules outside the cell. Like other bulk transport mechanisms, exocytosis requires energy.
Exocytosis is the opposite of endocytosis, which brings molecules inside the cell. Sometimes, the released materials are signaling molecules. For example, neurons typically use exocytosis to release neurotransmitters. Cells also use exocytosis to insert proteins such as ion channels into their cell membranes, secrete proteins for use in the extracellular matrix, or...
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Synaptic Signaling01:09

Synaptic Signaling

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Neurons communicate at synapses, or junctions, to excite or inhibit the activity of other neurons or target cells, such as muscles. Synapses may be chemical or electrical.
Most synapses are chemical, meaning an electrical impulse or action potential spurs the release of chemical messengers called neurotransmitters. The neuron sending the signal is called the presynaptic neuron, and the neuron receiving the signal is the postsynaptic neuron.
The presynaptic neuron fires an action potential that...
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Synaptic Signaling01:12

Synaptic Signaling

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Neurons communicate at synapses, or junctions, to excite or inhibit the activity of other neurons or target cells, such as muscles. Synapses may be chemical or electrical.
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Pinching-off of Coated Vesicles01:32

Pinching-off of Coated Vesicles

3.1K
Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
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Chemical Synapses01:26

Chemical Synapses

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Chemical synapses are specialized sites between two neurons or between a neuron and a non-neuronal cell like a muscle, glandular or sensory cell.
Because chemical synapses depend on the release of neurotransmitter molecules from synaptic vesicles to pass on their signal, there is an approximately one millisecond delay between when the axon potential reaches the presynaptic terminal and when the neurotransmitter leads to opening of postsynaptic ion channels. Additionally, this signaling is...
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Related Experiment Video

Updated: Apr 25, 2026

Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons
07:30

Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons

Published on: September 4, 2017

9.6K

Catching synaptic vesicles in action.

Thomas Schikorski1

  • 1Universidad Central del Caribe; Bayamon, Puerto Rico.

Communicative & Integrative Biology
|August 22, 2014
PubMed
Summary
This summary is machine-generated.

Electron microscopy initially revealed the synaptic vesicle cycle. However, fluorescent probes now offer superior kinetic analysis for live-cell studies, largely replacing older EM methods for this research.

Keywords:
clathrinelectron microscopyendocytosisendosomefast fixationkiss and runsynaptic vesicle retrieval

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

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An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins
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An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins

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Related Experiment Videos

Last Updated: Apr 25, 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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Examination of Synaptic Vesicle Recycling Using FM Dyes During Evoked, Spontaneous, and Miniature Synaptic Activities
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Examination of Synaptic Vesicle Recycling Using FM Dyes During Evoked, Spontaneous, and Miniature Synaptic Activities

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An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins
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An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins

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Area of Science:

  • Neuroscience
  • Cell Biology

Background:

  • The synaptic vesicle (SV) cycle, crucial for neurotransmission, was first observed using electron microscopy (EM) at the neuromuscular junction.
  • Traditional EM analysis provided structural insights but lacked the temporal resolution for detailed kinetic studies of the SV cycle.

Purpose of the Study:

  • To highlight the evolution of techniques for studying the synaptic vesicle cycle.
  • To emphasize the limitations of electron microscopy for kinetic analysis of the SV cycle in live cells.

Main Methods:

  • Review of historical techniques for synaptic vesicle research.
  • Comparison of electron microscopy (EM) with modern fluorescent probe methodologies.

Main Results:

  • Electron microscopy was instrumental in the initial discovery of the synaptic vesicle cycle.
  • Fluorescent probes enable real-time monitoring of cellular events, offering kinetic data unattainable with EM.
  • The advent of live-cell imaging with fluorescent probes has shifted the primary analytical approach away from EM for SV cycle kinetics.

Conclusions:

  • Modern fluorescent probe technology provides superior kinetic analysis of the synaptic vesicle cycle compared to traditional electron microscopy.
  • The field has advanced from static structural imaging to dynamic functional studies of synaptic vesicle trafficking.