Chelyshev Yurii A, Kabdesh Ilyas M, Mukhamedshina Yana O
Department of Histology, Cytology and Embryology, Kazan State Medical University, Kazan, Russia.
OpenLab Gene and Cell Technologies, Institute of Fundamental Medicine and Biology, Kazan (Volga Region) Federal University, Kremlevskaya St 18, Kazan, Tatarstan, Russia, 420008.
Cell Mol Neurobiol. 2022 Apr;42(3):647-664. doi: 10.1007/s10571-020-00986-0. Epub 2020 Oct 31.
The extracellular matrix (ECM) is a fundamental component of biological tissues. The ECM in the central nervous system (CNS) is unique in both composition and function. Functions such as learning, memory, synaptogenesis, and plasticity are regulated by numerous ECM molecules. The neural ECM acts as a non-specific physical barrier that modulates neuronal plasticity and axon regeneration. There are two specialized types of ECM in the CNS, diffuse perisynaptic ECM and condensed ECM, which selectively surround the perikaryon and initial part of dendritic trees in subtypes of neurons, forming perineuronal nets. This review presents the current knowledge about the role of important neuronal ECM molecules in maintaining the basic functions of a neuron, including electrogenesis and the ability to form neural circuits. The review mainly focuses on the role of ECM components that participate in the control of key events such as cell survival, axonal growth, and synaptic remodeling. Particular attention is drawn to the numerous molecular partners of the main ECM components. These regulatory molecules are integrated into the cell membrane or disposed into the matrix itself in solid or soluble form. The interaction of the main matrix components with molecular partners seems essential in molecular mechanisms controlling neuronal functions. Special attention is paid to the chondroitin sulfate proteoglycan 4, type 1 transmembrane protein, neural-glial antigen 2 (NG2/CSPG4), whose cleaved extracellular domain is such a molecular partner that it not only acts directly on neural and vascular cells, but also exerts its influence indirectly by binding to resident ECM molecules.
细胞外基质(ECM)是生物组织的基本组成部分。中枢神经系统(CNS)中的ECM在组成和功能上都很独特。学习、记忆、突触形成和可塑性等功能受多种ECM分子调控。神经ECM作为一种非特异性物理屏障,调节神经元可塑性和轴突再生。中枢神经系统中有两种特殊类型的ECM,即弥漫性突触周围ECM和浓缩ECM,它们选择性地围绕神经元亚型的胞体和树突树的起始部分,形成神经周网。本综述介绍了有关重要神经ECM分子在维持神经元基本功能(包括电发生和形成神经回路的能力)中作用的当前知识。综述主要关注参与控制细胞存活、轴突生长和突触重塑等关键事件的ECM成分的作用。特别关注主要ECM成分的众多分子伴侣。这些调节分子整合到细胞膜中或以固体或可溶形式置于基质本身中。主要基质成分与分子伴侣的相互作用在控制神经元功能的分子机制中似乎至关重要。特别关注硫酸软骨素蛋白聚糖4、1型跨膜蛋白、神经胶质抗原2(NG2/CSPG4),其裂解的细胞外结构域是这样一种分子伴侣,它不仅直接作用于神经和血管细胞,还通过与驻留的ECM分子结合间接发挥其影响。