相分离介导的区隔化是突触形成和可塑性的基础。

IF 12.1 1区 医学 Q1 NEUROSCIENCES
Xiandeng Wu, Zeyu Shen, Mingjie Zhang
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引用次数: 0

摘要

突触在其突触前和突触后两侧都是极化和高度区隔的。突触囊泡的区隔化,以及囊泡释放和循环机制,使得神经递质能够以精确控制的时间、速度和幅度释放。神经递质受体及其下游信号酶的区隔和集群组织允许神经元信号被正确接收和放大。突触粘附分子也形成簇状组装,排列突触前和突触后亚室,以促进突触的形成、稳定性和传递。最近的研究表明,这种突触和亚突触区隔组织是通过相分离形成的。本文综述了在突触形成和可塑性的背景下,这种浓缩的亚突触区室是如何形成和起作用的。我们讨论相分离如何允许在突触两侧形成多个不同的凝聚体,以及这些凝聚体如何相互交流。我们还强调了与稀释溶液中相同的蛋白质相比,蛋白质在凝聚相中如何表现出独特的性质。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phase Separation-Mediated Compartmentalization Underlies Synapse Formation and Plasticity.

The synapse is polarized and highly compartmentalized on both its pre- and postsynaptic sides. The compartmentalization of synaptic vesicles, as well as vesicle releasing and recycling machineries, allows neurotransmitters to be released with precisely controlled timing, speed, and amplitude. The compartmentalized and clustered organization of neurotransmitter receptors and their downstream signaling enzymes allows neuronal signals to be properly received and amplified. Synaptic adhesion molecules also form clustered assemblies to align pre- and postsynaptic subcompartments for synaptic formation, stability, and transmission. Recent studies indicate that such synaptic and subsynaptic compartmentalized organizations are formed via phase separation. This review discusses how such condensed subsynaptic compartments may form and function in the context of synapse formation and plasticity. We discuss how phase separation allows for the formation of multiple distinct condensates on both sides of a synapse and how such condensates communicate with each other. We also highlight how proteins display unique properties in condensed phases compared to the same proteins in dilute solutions.

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来源期刊
Annual review of neuroscience
Annual review of neuroscience 医学-神经科学
CiteScore
25.30
自引率
0.70%
发文量
29
期刊介绍: The Annual Review of Neuroscience is a well-established and comprehensive journal in the field of neuroscience, with a rich history and a commitment to open access and scholarly communication. The journal has been in publication since 1978, providing a long-standing source of authoritative reviews in neuroscience. The Annual Review of Neuroscience encompasses a wide range of topics within neuroscience, including but not limited to: Molecular and cellular neuroscience, Neurogenetics, Developmental neuroscience, Neural plasticity and repair, Systems neuroscience, Cognitive neuroscience, Behavioral neuroscience, Neurobiology of disease. Occasionally, the journal also features reviews on the history of neuroscience and ethical considerations within the field.
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