形成内啡林-Ca2+通道复合体对于克拉林介导的突触囊泡内分细胞形成至关重要
Yuan Chen1, Lunbin Deng, Yuka Maeno-Hikichi
1Department of Pharmacology, University of Pennsylvania School of Medicine, 3620 Hamilton Walk, Philadelphia, PA 19104, USA.
Cell
|October 9, 2003
概括
电压通道与内啡林直接相互作用,内啡林是一种对突触囊泡内细胞分裂至关重要的蛋白质. 这种依赖的相互作用将的流入与神经末端的囊泡循环联系起来.
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
- 分子生物学分子生物学
背景情况:
- 突触囊泡循环,包括外细胞和内细胞,对神经元功能至关重要.
- 电压通道 (VGCCs) 调节神经递质释放 (外细胞).
- 和VGCCs对囊泡内细胞的调节仍然不太了解.
研究的目的:
- 调查VGCCs在突触囊泡内分细胞的作用.
- 为了确定VGCC和内细胞机械之间的分子联系.
- 阐明影响内细胞分裂的机制.
主要方法:
- 同免疫沉检测蛋白质相互作用.
- 依赖结合测试. 依赖结合测试.
- 在海马神经元中进行电生理学和光染料吸收试验 (FM 4-64).
- 主导-负内啡林结构的表达.
主要成果:
- 发现了VGCCs和内分泌素之间的直接,依赖的相互作用.
- 内基素含有主要的结合域,调节VGCC-内基素和内基素-动氨酸复合体.
- 这种相互作用的抑制损害了克拉特林介导的内细胞形成,但没有影响外细胞形成.
结论:
- VGCC直接参与协调突触囊泡循环.
- 这项研究揭示了一种新的机制,通过内分泌素将流入与突触囊泡内分泌细胞结合.
- 这一发现凸显了VGCC在维持突触平稳中发挥的关键作用.
相关概念视频
Receptor-mediated Endocytosis
Overview
Receptor-mediated Endocytosis
Receptor-mediated endocytosis is when bulk amounts of specific molecules are imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle.
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...
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...
Pinching-off of Coated Vesicles
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...
Clathrin Coated Vesicles
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...
Receptor-Mediated Endocytosis
Receptor-mediated endocytosis is when bulk amounts of specific molecules are imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle.
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...


