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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.
132.8K
Electron Microscope Tomography and Single-particle Reconstruction01:07

Electron Microscope Tomography and Single-particle Reconstruction

2.8K
Transmission electron microscopy (TEM) can be used to determine the 3D structure of biological samples with the help of techniques such as electron microscope tomography and single-particle reconstruction. While single-particle reconstruction can examine macromolecules and macromolecular complexes in vitro conditions only, tomography permits the study of cell components or small cells in vivo.
Electron Tomography
Electron tomography can be performed either in TEM or STEM (scanning transmission...
2.8K
Postsynaptic Potential (PSP)01:32

Postsynaptic Potential (PSP)

4.9K
Postsynaptic potential (PSP) refers to a change in the electrical potential of a neuron when neurotransmitters released by presynaptic neurons bind to postsynaptic receptors. This potential can either be excitatory, leading to depolarization and ultimately action potential generation, or inhibitory, leading to hyperpolarization and suppression of the postsynaptic neuron.
There are two types of receptors: ionotropic and metabotropic.
The ionotropic receptor is the membrane protein that has an...
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Excitatory and Inhibitory Effects of Neurotransmitters01:29

Excitatory and Inhibitory Effects of Neurotransmitters

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When an action potential reaches the presynaptic axon terminal, it releases neurotransmitters from the neuron into the synaptic cleft at a chemical synapse. The released neurotransmitter can be excitatory or inhibitory. The critical criteria commonly used to determine whether a molecule is a neurotransmitter at a chemical synapse are the molecule's presence in the presynaptic neuron. Second, its release is in response to strong presynaptic depolarization. And lastly, the presence of...
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Chemical Synapses01:26

Chemical Synapses

11.3K
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...
11.3K
Chemical Synapses01:26

Chemical Synapses

4.4K
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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Video Experimental Relacionado

Updated: Jan 23, 2026

Evaluation of Synapse Density in Hippocampal Rodent Brain Slices
07:44

Evaluation of Synapse Density in Hippocampal Rodent Brain Slices

Published on: October 6, 2017

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Visualización de la Densidad Postsináptica en Sinapsis Excitatorias con Tomografía Electrónica

Rong Sun1,2,3,4, Qiangjun Zhou5,6,7,8

  • 1Vanderbilt Brain Institute, Vanderbilt University, Nashville, TN, USA.

Advances in neurobiology
|January 22, 2026
PubMed
Resumen
Este resumen es generado por máquina.

La tomografía electrónica (TE) proporciona vistas 3D de la ultraestructura sináptica con resolución nanométrica. Este método, especialmente la TE criogénica, revela la organización a nanoescala de las densidades postsinápticas, avanzando en neurociencia.

Palabras clave:
Tomografía electrónicaOrganización a nanoescalaDensidad postsinápticaSinapsisAlineación transinápticaMicroscopía electrónica de transmisión

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Micropatterning Transmission Electron Microscopy Grids to Direct Cell Positioning within Whole-Cell Cryo-Electron Tomography Workflows
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Last Updated: Jan 23, 2026

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Área de la Ciencia:

  • Neurociencia
  • Biología Celular
  • Biología Estructural

Sus antecedentes:

  • La microscopía electrónica convencional proporcionó información limitada sobre la ultraestructura sináptica.
  • La comprensión de la organización a nanoescala de las sinapsis es crucial para la neurociencia.

Objetivo del estudio:

  • Proporcionar una descripción detallada de las técnicas de tomografía electrónica (TE) para estudiar la ultraestructura sináptica.
  • Destacar la aplicación de la TE criogénica para la visualización casi nativa de sinapsis.
  • Explorar las ideas sobre la organización de la densidad postsináptica y la complejidad de las sinapsis excitatorias.

Principales métodos:

  • Introducción a los principios de la tomografía electrónica.
  • Explicación detallada de la preparación de muestras, la recopilación de datos y el procesamiento de imágenes para TE.
  • Énfasis en la tomografía electrónica criogénica (cryo-ET) para muestras biológicas.

Principales resultados:

  • La TE permite la reconstrucción 3D de alta resolución de la ultraestructura sináptica.
  • La TE criogénica permite la visualización de muestras biológicas en un estado casi nativo.
  • Se han obtenido información importante sobre la organización a nanoescala de las sinapsis excitatorias.

Conclusiones:

  • La tomografía electrónica es una herramienta fundamental para avanzar en la investigación de la biología sináptica.
  • El potencial futuro de la TE en neurociencia es sustancial.
  • La TE mejora significativamente la comprensión de la estructura y función sináptica.