Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

The Synapse02:47

The Synapse

132.8K
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...
4.9K
Excitatory and Inhibitory Effects of Neurotransmitters01:29

Excitatory and Inhibitory Effects of Neurotransmitters

12.7K
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...
12.7K
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...
4.4K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Regulation of spontaneous neurotransmission and homeostatic synaptic plasticity by synaptotagmin-1 disease variants at the SNARE primary interface.

bioRxiv : the preprint server for biology·2026
Same author

Fully genetically encoded low-molecular-weight protein tags with defined shapes for direct molecular identification by cryo-electron tomography.

bioRxiv : the preprint server for biology·2026
Same author

Glia-derived noncanonical fatty acid binding protein modulates brain lipid storage and clearance.

Science advances·2025
Same author

The postsynaptic density in excitatory synapses is composed of clustered, heterogeneous nanoblocks.

The Journal of cell biology·2025
Same author

Metal Ion Modulated Electron Transfer in Metalloviologen Compounds: Photochromism and Differentiable Amine Detection.

Inorganic chemistry·2024
Same author

Enhancing prostate cancer segmentation on multiparametric magnetic resonance imaging with background information and gland masks.

Medical physics·2024
Same journal

Correction to: Recent Structural Insights into the Molecular Architecture of Synapses.

Advances in neurobiology·2026
Same journal

Roles of Glia in Synapse Nano-organization.

Advances in neurobiology·2026
Same journal

Optical Approaches to Dissect the Structure and Dynamics of the Synapse at Nanoscale Resolution.

Advances in neurobiology·2026
Same journal

Functional Nano-segregation of Distinct Forms of Neurotransmission.

Advances in neurobiology·2026
Same journal

Scales of Postsynaptic Nanostructure: Molecules, Nanoclusters, and Nanodomains.

Advances in neurobiology·2026
Same journal

Synaptic Cell Adhesion: A Structural Perspective.

Advances in neurobiology·2026
查看所有相关文章

相关实验视频

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

18.0K

在激发性突触中可视化后突触密度,使用电子断层扫描.

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
概括
此摘要是机器生成的。

电子断层扫描 (ET) 提供了纳米分辨率3D视图的突触超结构. 这种方法,特别是冷ET,揭示了后突触密度的纳米组织,推进了神经科学.

关键词:
电子断层扫描是一种电子断层扫描.纳米规模组织组织.后突触密度 后突触密度 后突触密度突触突触是一个突触突触.跨突触对齐的调整传输电子显微镜的使用

更多相关视频

Visualization of ATP Synthase Dimers in Mitochondria by Electron Cryo-tomography
10:39

Visualization of ATP Synthase Dimers in Mitochondria by Electron Cryo-tomography

Published on: September 14, 2014

30.9K
Micropatterning Transmission Electron Microscopy Grids to Direct Cell Positioning within Whole-Cell Cryo-Electron Tomography Workflows
09:53

Micropatterning Transmission Electron Microscopy Grids to Direct Cell Positioning within Whole-Cell Cryo-Electron Tomography Workflows

Published on: September 13, 2021

7.6K

相关实验视频

Last 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

18.0K
Visualization of ATP Synthase Dimers in Mitochondria by Electron Cryo-tomography
10:39

Visualization of ATP Synthase Dimers in Mitochondria by Electron Cryo-tomography

Published on: September 14, 2014

30.9K
Micropatterning Transmission Electron Microscopy Grids to Direct Cell Positioning within Whole-Cell Cryo-Electron Tomography Workflows
09:53

Micropatterning Transmission Electron Microscopy Grids to Direct Cell Positioning within Whole-Cell Cryo-Electron Tomography Workflows

Published on: September 13, 2021

7.6K

科学领域:

  • 神经科学是一个神经科学.
  • 细胞生物学 细胞生物学
  • 结构生物学 结构生物学

背景情况:

  • 传统的电子显微镜对突触超结构的洞察力有限.
  • 了解纳米级突触组织对于神经科学至关重要.

研究的目的:

  • 为研究突触超结构提供电子断层扫描 (ET) 技术的详细概述.
  • 要突出冷ET的应用,用于近原生可视化突触.
  • 探索对 postsynaptic 密度组织和激发性突触复杂性的洞察.

主要方法:

  • 介绍电子断层扫描的原理.
  • 详细解释ET的样本准备,数据收集和图像处理.
  • 重点是生物样本的冷电子断层扫描 (cryo-ET).

主要成果:

  • ET可实现突触超结构的高分辨率3D重建.
  • 化ET允许在近乎原生状态下可视化生物样本.
  • 已经获得了关于激发性突触的纳米组织的重要见解.

结论:

  • 电子断层扫描是推动突触生物学研究的关键工具.
  • 在神经科学中ET的未来潜力是相当大的.
  • ET显著提高了对突触结构和功能的理解.