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

Fusion of Secretory Vesicles with the Plasma Membrane01:26

Fusion of Secretory Vesicles with the Plasma Membrane

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...
Ligand-Gated Ion Channel Receptor: Gating Mechanism01:30

Ligand-Gated Ion Channel Receptor: Gating Mechanism

Ligand-gated ion channels are transmembrane proteins that play a vital role in intercellular communication and functions of the nervous system. They allow the influx of ions across the membrane once the neurotransmitter binds, allowing the subsequent transmission of electrical excitation across the neurons. Other ligand-gated ion channels, like the γ-aminobutyric acid (GABA) receptor, permit anions like chloride into the cells on the binding of the GABA molecule. Their entry into the cell...
Chemical Synapses01:26

Chemical Synapses

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...
Chemical Synapses01:26

Chemical Synapses

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...
Excitatory and Inhibitory Effects of Neurotransmitters01:29

Excitatory and Inhibitory Effects of Neurotransmitters

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 specific...
Feedback Regulation of Calcium Concentration01:27

Feedback Regulation of Calcium Concentration

Calcium is an essential signaling molecule required for various cellular functions. Calcium pumps and ion channels on cell and organellar membranes, such as those on the endoplasmic reticulum (ER), regulate calcium concentrations inside the cell. They remain closed, keeping the cytosolic calcium levels low at a resting state.
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...

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

Tachykinin 1 neurons in the lateral habenula signal negative reward prediction error.

Current biology : CB·2026
Same author

Opioid withdrawal engages a habenular subpopulation responsive to aversive states.

bioRxiv : the preprint server for biology·2026
Same author

Tachykinin 1-expressing neurons in the lateral habenula signal negative reward prediction error.

bioRxiv : the preprint server for biology·2025
Same author

Safety and Efficacy of Senolytic UBX1325 in Diabetic Macular Edema.

NEJM evidence·2025
Same author

Multifocal Electroretinography Changes after UBX1325 (Foselutoclax) Treatment in Neovascular Age-Related Macular Degeneration.

Journal of clinical medicine·2024
Same author

Therapeutic targeting of cellular senescence in diabetic macular edema: preclinical and phase 1 trial results.

Nature medicine·2024

相关实验视频

Updated: May 18, 2026

Dopamine Release at Individual Presynaptic Terminals Visualized with FFNs
09:37

Dopamine Release at Individual Presynaptic Terminals Visualized with FFNs

Published on: August 31, 2009

Elfn1调节CA1-内核神经元突触中的特定目标释放概率.

Emily L Sylwestrak1, Anirvan Ghosh

  • 1Neurobiology Section, Division of Biological Sciences, University of California, San Diego, La Jolla, CA 92093-0366, USA.

Science (New York, N.Y.)
|October 9, 2012
PubMed
概括

在O-LM内部神经元中含有1 (Elfn1) 蛋白质的细胞外白丰富的重复纤维素指导突触形成. 后突触Elfn1控制了前突触释放的概率,创造了特定的金字塔-O-LM突触特性.

科学领域:

  • 神经科学是一个神经科学.
  • 突触性可塑性 突触性可塑性
  • 分子生物学分子生物学

背景情况:

  • 突触传输可以涉及针对特定突触属性的双向信号传输.
  • 金字塔神经元在海马内部神经元上形成不同的刺激突触.
  • 对O-LM内部神经元的突触是促进的 (释放概率低),而对parvalbumin内部神经元的突触是抑制的 (释放概率高).

研究的目的:

  • 调查潜在的特定目标突触形成的分子机制.
  • 确定含有1 (Elfn1) 的细胞外白丰富重复纤维素在调节突触性质中的作用.

主要方法:

  • 在海马内部神经元中对Elfn1的选择性表达分析.
  • 电生理学记录以评估突触释放概率.
  • 研究Elfn1对突触形成和性质的功能影响.

主要成果:

  • 含有1 (Elfn1) 的细胞外白素丰富的重复纤维素被oriens-lacunosum moleculare (O-LM) 内神经元选择性地表达.
  • 后突触Elfn1的表达调节了前突触释放的概率.
  • 这种调节指导了促进金字塔-O-LM突触的形成.

更多相关视频

Whole-cell Patch-clamp Recordings from Morphologically- and Neurochemically-identified Hippocampal Interneurons
14:37

Whole-cell Patch-clamp Recordings from Morphologically- and Neurochemically-identified Hippocampal Interneurons

Published on: September 30, 2014

Presynapse Formation Assay Using Presynapse Organizer Beads and “Neuron Ball” Culture
10:17

Presynapse Formation Assay Using Presynapse Organizer Beads and “Neuron Ball” Culture

Published on: August 2, 2019

相关实验视频

Last Updated: May 18, 2026

Dopamine Release at Individual Presynaptic Terminals Visualized with FFNs
09:37

Dopamine Release at Individual Presynaptic Terminals Visualized with FFNs

Published on: August 31, 2009

Whole-cell Patch-clamp Recordings from Morphologically- and Neurochemically-identified Hippocampal Interneurons
14:37

Whole-cell Patch-clamp Recordings from Morphologically- and Neurochemically-identified Hippocampal Interneurons

Published on: September 30, 2014

Presynapse Formation Assay Using Presynapse Organizer Beads and “Neuron Ball” Culture
10:17

Presynapse Formation Assay Using Presynapse Organizer Beads and “Neuron Ball” Culture

Published on: August 2, 2019

结论:

  • 在O-LM内部神经元中Elfn1的后突触表达对于确定特定目标的突触性质至关重要.
  • Elfn1 作为一个信号分子从 postsynaptic 神经元调节 presynaptic 释放概率.
  • 这种机制赋予了针对O-LM内部神经元的金字塔细胞轴突独特的功能特征.