Synaptic proteomics decode novel molecular landscape in the brain

Yuki Ito, Sayaka Nagamoto, Tetsuya Takano
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Abstract

Synapses play a pivotal role in forming neural circuits, with critical implications for brain functions such as learning, memory, and emotions. Several advances in synaptic research have demonstrated the diversity of synaptic structure and function, which can form thousands of connections depending on the neuronal cell types. Moreover, synapses not only interconnect neurons but also establish connections with glial cells such as astrocytes, which play a key role in the architecture and function of neuronal circuits in the brain. Emerging evidence suggests that dysfunction of synaptic proteins contributes to a variety of neurological and psychiatric disorders. Therefore, it is crucial to determine the molecular networks within synapses in various neuronal cell types to gain a deeper understanding of how the nervous system regulates brain function. Recent advances in synaptic proteome approaches, such as fluorescence-activated synaptosome sorting (FASS) and proximity labeling, have allowed for a detailed and spatial analysis of many cell-type-specific synaptic molecules in vivo. In this brief review, we highlight these novel spatial proteomic approaches and discuss the regulation of synaptic formation and function in the brain. This knowledge of molecular networks provides new insight into the understanding of many neurological and psychiatric disorders.
突触蛋白质组学解码大脑中的新分子景观
突触在形成神经回路方面起着关键作用,对学习、记忆和情感等大脑功能有着重要影响。突触研究的一些进展证明了突触结构和功能的多样性,根据神经元细胞类型的不同,突触可形成数千种连接。此外,突触不仅能使神经元相互连接,还能与神经胶质细胞(如星形胶质细胞)建立连接。新的证据表明,突触蛋白的功能障碍会导致多种神经和精神疾病。因此,确定各种神经元细胞类型中突触内的分子网络对于深入了解神经系统如何调节大脑功能至关重要。荧光激活突触小体分选(FASS)和邻近标记等突触蛋白质组方法的最新进展使我们能够在体内对许多细胞类型特异的突触分子进行详细的空间分析。在这篇简短的综述中,我们将重点介绍这些新颖的空间蛋白质组学方法,并讨论大脑中突触形成和功能的调控。这种分子网络知识为了解许多神经和精神疾病提供了新的视角。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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