突触囊泡位置对释放概率和外细胞融合模式的影响
Hyokeun Park1, Yulong Li, Richard W Tsien
1Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA.
概括
研究人员开发了一种用于实时跟踪单个突触囊泡的新方法,揭示了它们的位置和运动如何影响神经传递和融合模式,如吻和跑与完全崩.
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:
- 神经传递依赖于在前突触终端内的突触囊泡动力学.
- 精确的,纳米尺度监测这些囊泡运动一直是一个重大挑战.
研究的目的:
- 开发和应用一种高精度,实时跟踪单个突触囊泡的方法.
- 研究神经传递过程中囊泡位置,运动和融合事件之间的关系.
主要方法:
- 使用量子点 (Qdot) 装载的突触囊泡进行三维实时跟踪.
- 在囊泡定位方面获得纳米级精度 (20-30nm).
- 采用Qdot光的试蓝火法来确定聚变事件和模式.
主要成果:
- 位置靠近聚变点的气囊表现出早期的聚变.
- 融合的模式 (亲吻和逃跑与完全崩) 取决于囊泡的先前运动.
- 接吻和逃跑的聚变发生在中心,而完全崩的聚变分布更广泛.
结论:
- 囊泡接近融合部位和先前的动态是神经递质释放的关键决定因素.
- 该研究为突触囊泡融合机制提供了前所未有的时空洞察力.
- 这种技术为研究突触功能和功能障碍提供了强大的工具.
相关概念视频
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...
In 1993, Jim Rothman proposed that the antiparallel pairing of vesicular and transmembrane SNAREs, or...
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...
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
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...
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...
Exocytosis
Exocytosis is used to release material from cells. Like other bulk transport mechanisms, exocytosis requires energy.
SNAREs and Membrane Fusion
Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
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...
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...


