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Related Concept Videos

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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Vesicular Tubular Clusters01:45

Vesicular Tubular Clusters

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After budding out from the ER membrane, some COPII vesicles lose their coat and fuse with one another to form larger vesicles and interconnected tubules called vesicular tubular clusters or VTCs. These clusters constitute a compartment at the ER-Golgi interface known as ERGIC (Endoplasmic Reticulum Golgi Intermediate Compartment). The ERGIC is a mobile membrane-bound cargo transport system that sorts proteins secreted from ER and delivers them to the Golgi.
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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.
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Chemical Synapses01:26

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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.
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Overview of Secretory Vesicles01:33

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Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
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SNAREs and Membrane Fusion01:43

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Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
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Related Experiment Video

Updated: Jun 11, 2025

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins
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The synaptic vesicle cluster as a controller of pre- and postsynaptic structure and function.

Sofiia Reshetniak1, Cristian A Bogaciu1, Stefan Bonn2

  • 1Institute for Neuro- and Sensory Physiology and Biostructural Imaging of Neurodegeneration (BIN) Center, University Medical Center Göttingen, Göttingen, Germany.

The Journal of Physiology
|October 5, 2024
PubMed
Summary
This summary is machine-generated.

The synaptic vesicle cluster (SVC) regulates synapse structure and function by controlling neurotransmitter release and organizing key proteins. Its size changes with the postsynaptic compartment, highlighting its role in synaptic plasticity and metabolism.

Keywords:
synapsesynapse formationsynaptic plasticitysynaptic vesicle clustervesicle

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Last Updated: Jun 11, 2025

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Area of Science:

  • Neuroscience
  • Cell Biology
  • Synaptic Physiology

Background:

  • The synaptic vesicle cluster (SVC) is crucial for neurotransmitter release at chemical synapses.
  • SVCs also sequester proteins involved in exo- and endocytosis, influencing local molecular concentrations.
  • SVCs interact with organelles like mitochondria and the endoplasmic reticulum, affecting synaptic metabolism.

Purpose of the Study:

  • To highlight the multifaceted role of the SVC beyond neurotransmitter storage.
  • To propose the SVC as a central regulator of synaptic structure, function, and plasticity.
  • To emphasize the coordinated dynamics between SVC size and postsynaptic structures.

Main Methods:

  • Review and synthesis of existing literature on SVC composition and function.
  • Analysis of the SVC's impact on synaptic signaling, plasticity, and metabolism.
  • Conceptual framework development for SVC as a regulatory hub.

Main Results:

  • The SVC actively organizes cytoskeletal components, adhesion proteins, and organelles.
  • SVCs influence synapse formation, stabilization, signaling, and plasticity.
  • SVC size variations correlate with postsynaptic compartment changes, indicating pre- and postsynaptic coupling.

Conclusions:

  • The SVC acts as an 'all-in-one' regulator of synaptic architecture and function.
  • Further investigation into SVC molecular mechanisms is needed to understand synaptic heterogeneity.
  • The SVC's role in synaptic metabolism and plasticity warrants deeper exploration.