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 Role of Ion Channels in Neuronal Computation01:19

The Role of Ion Channels in Neuronal Computation

3.2K
A postsynaptic neuron usually receives numerous impulses from several other presynaptic neurons. The axon hillock of the postsynaptic neuron integrates all these signals and determines the likelihood of firing an action potential.
Sometimes a single EPSP is strong enough to induce an action potential in the postsynaptic neuron. However, multiple presynaptic inputs must often create EPSPs around the same time for the postsynaptic neuron to be sufficiently depolarized to fire an action potential....
3.2K
Chemical Synapses01:26

Chemical Synapses

9.5K
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...
9.5K
Feedback Regulation of Calcium Concentration01:27

Feedback Regulation of Calcium Concentration

2.9K
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...
2.9K
Calmodulin-dependent Signaling01:16

Calmodulin-dependent Signaling

5.0K
Calmodulin (CaM) is a calcium-binding protein in eukaryotes that controls various calcium-regulated cellular processes. It has four calcium-binding sites that bind calcium to form the calcium-calmodulin ( Ca2+-CaM) complex. GPCR stimulation increases the calcium levels in the cells that bind to CaM and induces a conformational change.
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
5.0K
Relaxation of Skeletal Muscles01:29

Relaxation of Skeletal Muscles

9.6K
The period of muscle contraction primarily influences the duration of stimulation at the neuromuscular junction (NMJ), the presence of free calcium ions in the sarcoplasm, and the availability of energy or ATP to support contractions.
When an action potential reaches the axon terminal, it depolarizes the membrane and opens voltage-gated sodium channels. Sodium ions enter the cell, further depolarizing the presynaptic membrane. This depolarization causes voltage-gated calcium channels to open....
9.6K
Chemical Synapses01:26

Chemical Synapses

10.9K
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...
10.9K

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

Revisiting adult neurogenesis and the role of erythropoietin for neuronal and oligodendroglial differentiation in the hippocampus.

Molecular psychiatry·2016
Same author

Venus Flytrap HKT1-Type Channel Provides for Prey Sodium Uptake into Carnivorous Plant Without Conflicting with Electrical Excitability.

Molecular plant·2015
Same author

Introduction: regulated exocytosis.

Cell calcium·2012
Same author

Kinetics of both synchronous and asynchronous quantal release during trains of action potential-evoked EPSCs at the rat calyx of Held.

The Journal of physiology·2007
Same author

Optimizing imaging parameters for the separation of multiple labels in a fluorescence image.

Journal of microscopy·2003
Same author

Calcium signals and synaptic short-term plasticity in the central nervous system.

Anales de la Real Academia Nacional de Medicina·2002

相关实验视频

Updated: May 3, 2026

Loading a Calcium Dye into Frog Nerve Endings Through the Nerve Stump: Calcium Transient Registration in the Frog Neuromuscular Junction
17:05

Loading a Calcium Dye into Frog Nerve Endings Through the Nerve Stump: Calcium Transient Registration in the Frog Neuromuscular Junction

Published on: July 8, 2017

10.0K

在快速的中央突触中,发射器释放率的细胞内依赖性.

R Schneggenburger1, E Neher

  • 1Abteilung Membranbiophysik, Max-Planck-Institut für biophysikalische Chemie, Göttingen, Germany. rschneg@gwdg.de

Nature
|September 6, 2000
PubMed
概括

快速释放的神经递质依赖于. 这项研究表明,低细胞内水平 (10微米) 引发了中枢神经系统突触中的快速囊泡融合和释放.

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
  • 生物物理学的生物物理.

背景情况:

  • 突触囊泡融合和神经递质释放对于神经元信号传递至关重要.
  • 快速释放的神经递质被认为需要高局部细胞内度 ([Ca2+]i>100微米).
  • 在突触释放部位缺乏局部[Ca2+]i的实验估计.

研究的目的:

  • 通过实验确定快速释放神经递质所需的局部细胞内度 ([Ca2+]i).
  • 为了研究结合和囊泡融合的动力学.
  • 了解快速突触传输对的敏感性.

主要方法:

  • 离子在大型突触终端 (赫尔德的玻璃杯) 中脱.
  • 在受控[Ca2+]i步骤后,神经递质释放速率的动态分析.
  • 测量囊泡池耗尽的情况.

主要成果:

  • [Ca2+]i的阶段式升高到10微米诱导了快速发射器释放.
  • 大约80%的可用囊泡在不到3个月的时间内被耗尽.
  • 过渡的[Ca2+]i升高到25微米可以解释单次作用电位期间的释放.
  • 传感器在正常释放概率下没有和.

更多相关视频

Fluorescent Calcium Imaging and Subsequent In Situ Hybridization for Neuronal Precursor Characterization in Xenopus laevis
09:07

Fluorescent Calcium Imaging and Subsequent In Situ Hybridization for Neuronal Precursor Characterization in Xenopus laevis

Published on: February 18, 2020

9.4K
Registration of Calcium Transients in Mouse Neuromuscular Junction with High Temporal Resolution using Confocal Microscopy
11:12

Registration of Calcium Transients in Mouse Neuromuscular Junction with High Temporal Resolution using Confocal Microscopy

Published on: December 1, 2021

1.6K

相关实验视频

Last Updated: May 3, 2026

Loading a Calcium Dye into Frog Nerve Endings Through the Nerve Stump: Calcium Transient Registration in the Frog Neuromuscular Junction
17:05

Loading a Calcium Dye into Frog Nerve Endings Through the Nerve Stump: Calcium Transient Registration in the Frog Neuromuscular Junction

Published on: July 8, 2017

10.0K
Fluorescent Calcium Imaging and Subsequent In Situ Hybridization for Neuronal Precursor Characterization in Xenopus laevis
09:07

Fluorescent Calcium Imaging and Subsequent In Situ Hybridization for Neuronal Precursor Characterization in Xenopus laevis

Published on: February 18, 2020

9.4K
Registration of Calcium Transients in Mouse Neuromuscular Junction with High Temporal Resolution using Confocal Microscopy
11:12

Registration of Calcium Transients in Mouse Neuromuscular Junction with High Temporal Resolution using Confocal Microscopy

Published on: December 1, 2021

1.6K

结论:

  • 快速神经递质释放可以由较低的[Ca2+]i触发,而不是以前假设的.
  • 高合作性和传感器的不和度提高了突触传输的灵敏度.
  • 暂时的局部信号足以快速的突触传输.