VAPB轴精确地协调了在神经地图发育过程中发动神经元形发生的时间
Daichi Kamiyama1, Yuri Nishida1, Rie Kamiyama1
1University of Georgia.
Research square
|January 13, 2025
概括
研究人员发现,Eph受体和VAMP相关蛋白33 (Vap33) 调节Cdc42激活,控制Drosophila运动神经元中的树突发育. 这种信号通路与人类运动神经元疾病 (如ALS8和SMA) 有关.
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
- 发展生物学 发展生物学
背景情况:
- 在Drosophila运动神经元中的时空 dendritic 模式对于神经电路的形成至关重要.
- 调节树枝状发育时间方面的机制在很大程度上是未知的.
- Cdc42 GTPase之前被确定为这个过程中的一个关键的行为因子调节器.
研究的目的:
- 为了识别Drosophila运动神经元中激活Cdc42的上游因素.
- 阐明将细胞外线线索与细胞内Cdc42激活联系起来的信号通路.
- 研究VAMP相关蛋白33 (Vap33) 在树突发育的时间调节中的作用.
主要方法:
- 在Drosophila的单细胞遗传学.
- 基于振荡能量转移 (FRET) 的成像.
- 生物化学技术分析蛋白质相互作用和激活状态.
主要成果:
- 关氨酸核酸交换因子Vav由Eph受体氨酸激酶招募到血膜,导致Cdc42激活.
- 与VAMP相关的蛋白33 (Vap33),是一种Eph联体,非细胞自主分泌,并诱导Eph受体自化.
- Vap33从ER居住蛋白转换为细胞外线信号,信号Cdc42激活的时间.
结论:
- Vav,Eph受体和Vap33形成一个信号轴,暂时调节Cdc42激活的树突模式.
- 细胞外Vap33在运动神经元发育过程中起到时间信号的作用.
- 保存的人类正经体VAPB与运动神经元疾病 (ALS8,SMA) 有关,这突显了该途径的临床相关性.
更多相关视频
10:57Mouse Hindbrain Ex Vivo Culture to Study Facial Branchiomotor Neuron Migration
Published on: March 18, 2014
11.2K
08:48Stable and Efficient Genetic Modification of Cells in the Adult Mouse V-SVZ for the Analysis of Neural Stem Cell Autonomous and Non-autonomous Effects
Published on: February 17, 2016
9.2K
相关概念视频
Action Potential
7.7K
Neurons communicate by firing action potentials—the electrochemical signal that is propagated along the axon. The signal results in the release of neurotransmitters at axon terminals, thereby transmitting information to the nervous system. An action potential is a specific "all-or-none" change in membrane potential that results in a rapid spike in voltage.
Membrane potential in neurons
Neurons typically have a resting membrane potential of about -70 millivolts (mV). When they...
Membrane potential in neurons
Neurons typically have a resting membrane potential of about -70 millivolts (mV). When they...
7.7K
Assembly of Complex Microtubule Structures
1.8K
Complex microtubule structures are present in resting cells and in dividing cells. In resting cells, they are responsible for maintaining the cellular architecture, tracks for intracellular transport, positioning of organelles, assembly of cilia and flagella. They mediate the bipolar spindle assembly for chromosomal segregation and positioning of the cell division plate in dividing cells. The formation of microtubule complex structures depends on the cell type, cell stage, and cell function.
1.8K
Action Potentials
128.5K
Overview
128.5K
