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相关概念视频

Exocytosis00:50

Exocytosis

Exocytosis is a process that releases molecules outside the cell. Like other bulk transport mechanisms, exocytosis requires energy.
Exocytosis is the opposite of endocytosis, which brings molecules inside the cell. Sometimes, the released materials are signaling molecules. For example, neurons typically use exocytosis to release neurotransmitters. Cells also use exocytosis to insert proteins such as ion channels into their cell membranes, secrete proteins for use in the extracellular matrix, or...
Overview of Secretory Vesicles01:33

Overview of Secretory Vesicles

Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
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...
Vesicular Tubular Clusters01:45

Vesicular Tubular Clusters

After budding out from the ER membrane, some COPII vesicles lose their coat and fuse with one another to form larger vesicles and interconnected tubules called vesicular tubular clusters or VTCs. These clusters constitute a compartment at the ER-Golgi interface known as ERGIC (Endoplasmic Reticulum Golgi Intermediate Compartment). The ERGIC is a mobile membrane-bound cargo transport system that sorts proteins secreted from ER and delivers them to the Golgi.
With the help of motor proteins such...

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相关实验视频

Updated: Jun 22, 2026

Examination of Synaptic Vesicle Recycling Using FM Dyes During Evoked, Spontaneous, and Miniature Synaptic Activities
08:10

Examination of Synaptic Vesicle Recycling Using FM Dyes During Evoked, Spontaneous, and Miniature Synaptic Activities

Published on: March 31, 2014

STED显微镜显示,在突触囊泡脱细胞化后,突触胺仍然聚集在一起.

Katrin I Willig1, Silvio O Rizzoli, Volker Westphal

  • 1Departments of NanoBiophotonics, Max Planck Institute for Biophysical Chemistry, 37077 Göttingen, Germany.

Nature
|April 14, 2006
PubMed
概括

突触囊泡组件在融合后仍然聚集在一起,不会自由扩散. 这项研究使用超分辨率显微镜在回收过程中跟踪囊泡蛋白质,揭示了它们的空间组织.

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
  • 显微镜的使用方法

背景情况:

  • 突触传输依赖于通过突触囊泡的外细胞分裂释放的神经递质.
  • 膀膜通过内细胞结合和随后的再生来恢复,对于持续的神经传递至关重要.
  • 由于分辨率限制,在膜融合后突触囊泡组件的命运仍然不太清楚.

研究的目的:

  • 为了调查突触囊泡组件是否在异位细胞形成后保持集群或扩散.
  • 为了克服传统显微镜的分辨率限制,观察纳米级突触结构.
  • 在回收过程中确定囊泡蛋白的空间组织.

主要方法:

  • 利用刺激辐射消耗 (STED) 显微镜实现超高分辨率成像.
  • 将焦点区域显著降低到离散极限以下,以解决单个突触囊泡.
  • 追踪了囊泡膜蛋白质synaptotagmin I在突触前膜上的分布.

主要成果:

  • 观察到Synaptotagmin I仍然聚集在突触前膜上不同的斑块上.
  • 这些集群斑块不论神经末端活动水平 (轻度到强度刺激) 持续存在.
  • 证明了STED显微镜能够解决纳米级细胞结构 (约. 40nm) 的可见光.使用可见光.

更多相关视频

Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons
07:30

Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons

Published on: September 4, 2017

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins
09:33

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins

Published on: June 26, 2018

相关实验视频

Last Updated: Jun 22, 2026

Examination of Synaptic Vesicle Recycling Using FM Dyes During Evoked, Spontaneous, and Miniature Synaptic Activities
08:10

Examination of Synaptic Vesicle Recycling Using FM Dyes During Evoked, Spontaneous, and Miniature Synaptic Activities

Published on: March 31, 2014

Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons
07:30

Measuring Synaptic Vesicle Endocytosis in Cultured Hippocampal Neurons

Published on: September 4, 2017

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins
09:33

An Optical Assay for Synaptic Vesicle Recycling in Cultured Neurons Overexpressing Presynaptic Proteins

Published on: June 26, 2018

结论:

  • 至少一些突触囊泡组成部分在融合后和循环过程中保持其空间组织.
  • 这些发现挑战了囊泡成分在血上完全扩散的概念.
  • 突出了超分辨率STED显微镜在纳米级研究突触囊泡动力学的力量.