单片囊成像显示了在活性区域的囊泡的actin依赖的空间限制,这对于持续传播至关重要
Takafumi Miki1,2, Yuji Okamoto1, Miyuki Ueno-Umegai3
1Department of Cell Physiology, Graduate School of Medicine, Akita University, Akita 010-8543, Japan.
概括
动氨酸纤维对突触囊泡 (SV) 招募至关重要,确保持续的神经传递. 它们的存在,而不是动态,有助于在活跃区域附近快速重新加载SV,以提供高效的信号.
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
- 突触传输是突触传输的过程.
背景情况:
- 在高频率的持续神经递质释放依赖于突触囊泡 (SV) 重载.
- 在中央突触中重新加载SV的精确机制仍然不太清楚.
研究的目的:
- 为了研究actin filaments在SV招募和持续神经传递的流动性中的作用.
- 为了阐明 SV 在小脑的纤维终端重新加载的机制.
主要方法:
- 总内部反射光显微镜 (TIR-FM) 用于观察SVs.
- 用于监测膜融合的电容度测量.
- 单粒子追踪 (SPT) 使用量子点用于囊泡移动.
- 隐藏马尔科夫建模 (HMM) 用于扩散状态分析.
- F-actin 染色.F-actin 染色是一种染色.
主要成果:
- 动蛋白干扰取消了快速的SV招募,并减少了持续释放.
- 动氨酸聚合不会影响招募或释放,这表明光线的存在是关键.
- 动蛋白干扰增加了 SV 扩散率,从自由扩散和被困状态转移到主要自由扩散状态.
- 在活性区域外局部化的动氨酸丝,可能限制SVs.
结论:
- 动氨酸丝,而不是它们的动态,对于快速招募SV至关重要.
- 动氨酸纤维限制了SV扩散,促进了高效的招募,原始化和持续的突触传输.
相关概念视频
Pinching-off of Coated Vesicles
3.1K
Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
3.1K
Intracellular Movement of Viruses and Bacteria
2.8K
Intracellular bacteria and viruses often comprise a group of highly infectious pathogens that can cause several diseases. Bacterial pathogens include those belonging to the genus Rickettsia responsible for conditions such as rocky mountain spotted fever and the Mediterranean spotted fever; Chlamydia, a genus responsible for a sexually transmitted disease; Coxiella burnetii, an agent responsible for Q fever. Viral pathogens include vaccinia—a poxvirus, and herpes simplex virus—a...
2.8K
Clathrin Coated Vesicles
6.9K
Clathrin-coated vesicles use endocytosis to transport receptors and lysosomal hydrolases from the Golgi to the lysosome in the late secretory pathway. Clathrin-mediated endocytosis was the first described endocytic process, and Clathrin-coated vesicles remain one of the most well-studied transport vesicles. The molecular machinery that generates clathrin-coated vesicles comprises over 50 proteins that precisely coordinate vesicle formation. Cell surface receptors concentrated in indented sites...
6.9K
Overview of Secretory Vesicles
8.5K
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...
8.5K
Vesicular Tubular Clusters
2.5K
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...
With the help of motor proteins such...
2.5K
Intralumenal Vesicles and Multivesicular Bodies
3.4K
Intraluminal vesicles (ILVs) are small vesicles 50-80 nm in diameter formed during the maturation of early endosomes. A specialized endosome containing numerous ILVs is called a multivesicular body (MVB). ILVs contain internalized molecules such as antigens, nucleic acids, proteins, and metabolites. Some of these molecules are released from the MVBs inside exosomes and are transported to other cells. Other MVBs contain molecules that are retained in the ILVs and are later degraded within the...
3.4K


