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Related Concept Videos

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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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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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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The Synapse02:47

The Synapse

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Neurons communicate with one another by passing on their electrical signals to other neurons. A synapse is the location where two neurons meet to exchange signals. At the synapse, the neuron that sends the signal is called the presynaptic cell, while the neuron that receives the message is called the postsynaptic cell. Note that most neurons can be both presynaptic and postsynaptic, as they both transmit and receive information.
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Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein01:20

Antiepileptic Drugs: Modulators of Neurotransmitter Release Mediated by SV2A Protein

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Antiepileptic drugs, such as levetiracetam (Keppra) and brivaracetam (Briviact), have emerged as crucial tools in managing epilepsy. These medications exert their therapeutic effects by targeting the synaptic vesicle protein SV2A, a transmembrane glycoprotein primarily found in the brain.
SV2A is a transmembrane glycoprotein located predominantly in the brain, modulating the release of neurotransmitters for neuronal communication. Both levetiracetam and brivaracetam exhibit a high affinity for...
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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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Analyzing the Size, Shape, and Directionality of Networks of Coupled Astrocytes
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Astrocytes control synaptic strength by two distinct v-SNARE-dependent release pathways.

Yvonne Schwarz1, Na Zhao2, Frank Kirchhoff2

  • 1Molecular Neurophysiology, Center for Integrative Physiology and Molecular Medicine, Saarland University, Homburg, Germany.

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Summary

Astrocytes use distinct vesicular SNARE proteins to control brain signaling. Cellubrevin-mediated neuropeptide Y release reduces signaling, while synaptobrevin II-mediated glutamate release enhances it.

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Area of Science:

  • Neuroscience
  • Cell Biology
  • Molecular Biology

Background:

  • Glia-neuron communication is vital for brain function.
  • Molecular mechanisms of gliotransmission are not fully understood.

Purpose of the Study:

  • Investigate the roles of synaptobrevin II and cellubrevin in astrocytic release.
  • Elucidate the functional consequences of these pathways on neuronal signaling.

Main Methods:

  • Utilized null-mutants for Vamp2 (synaptobrevin II) and Vamp3 (cellubrevin).
  • Generated compound null-mutants for both genes.
  • Assessed astrocytic release processes and their impact on synaptic signaling.

Main Results:

  • Astrocytes express synaptobrevin II on glutamatergic vesicles and cellubrevin on NPY-containing vesicles.
  • Cellubrevin-dependent NPY release diminishes synaptic signaling.
  • Synaptobrevin II-dependent glutamate release enhances synaptic signaling.

Conclusions:

  • Identified two distinct v-SNARE-dependent astrocytic release pathways.
  • These pathways oppositely control synaptic strength.
  • Uncovered novel mechanisms of astrocyte-neuron communication.