了解突触的分子多样性。

Understanding the molecular diversity of synapses.

作者信息

van Oostrum Marc, Schuman Erin M

机构信息

Max Planck Institute for Brain Research, Frankfurt am Main, Germany.

Biozentrum, University of Basel, Basel, Switzerland.

出版信息

Nat Rev Neurosci. 2025 Feb;26(2):65-81. doi: 10.1038/s41583-024-00888-w. Epub 2024 Dec 5.

Abstract

Synapses are composed of thousands of proteins, providing the potential for extensive molecular diversity to shape synapse type-specific functional specializations. In this Review, we explore the landscape of synaptic diversity and describe the mechanisms that expand the molecular complexity of synapses, from the genotype to the regulation of gene expression to the production of specific proteoforms and the formation of localized protein complexes. We emphasize the importance of examining every molecular layer and adopting a systems perspective to understand how these interconnected mechanisms shape the diverse functional and structural properties of synapses. We explore current frameworks for classifying synapses and methodologies for investigating different synapse types at varying scales, from synapse-type-specific proteomics to advanced imaging techniques with single-synapse resolution. We highlight the potential of synapse-type-specific approaches for integrating molecular data with cellular functions, circuit organization and organismal phenotypes to enable a more holistic exploration of neuronal phenomena across different scales.

摘要

突触由数千种蛋白质组成,这为广泛的分子多样性提供了可能,从而塑造特定突触类型的功能特化。在本综述中,我们探索突触多样性的全貌,并描述从基因型到基因表达调控,再到特定蛋白质异构体的产生以及局部蛋白质复合物形成等扩大突触分子复杂性的机制。我们强调审视每一个分子层面并采用系统观点的重要性,以了解这些相互关联的机制如何塑造突触多样的功能和结构特性。我们探索当前用于突触分类的框架以及在不同尺度上研究不同突触类型的方法,从特定突触类型的蛋白质组学到具有单突触分辨率的先进成像技术。我们强调特定突触类型方法在整合分子数据与细胞功能、神经回路组织和生物体表型方面的潜力,以便能够在不同尺度上更全面地探索神经元现象。

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