Synaptic plasticity-associated proteases and protease inhibitors in the brain linked to the processing of extracellular matrix and cell adhesion molecules.

Neuron glia biology Pub Date : 2008-08-01 Epub Date: 2009-08-13 DOI:10.1017/S1740925X09990172
Tet Woo Lee, Vicky W K Tsang, Nigel P Birch
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引用次数: 34

Abstract

Research on the molecular and cellular basis of learning and memory has focused on the mechanisms that underlie the induction and expression of synaptic plasticity. There is increasing evidence that structural changes at the synapse are associated with synaptic plasticity and that extracellular matrix (ECM) components and cell adhesion molecules are associated with these changes. The functions of both groups of molecules can be regulated by proteolysis. In this article we review the roles of selected proteases and protease inhibitors in perisynaptic proteolysis of the ECM and synaptic adhesion proteins and the impact of proteolysis on synaptic modification and cognitive function.

大脑突触可塑性相关蛋白酶和蛋白酶抑制剂与细胞外基质和细胞粘附分子的加工有关。
学习和记忆的分子和细胞基础研究主要集中在突触可塑性诱导和表达的机制上。越来越多的证据表明突触的结构变化与突触可塑性有关,细胞外基质(ECM)成分和细胞粘附分子与这些变化有关。这两组分子的功能都可以通过蛋白水解来调节。在这篇文章中,我们综述了选定的蛋白酶和蛋白酶抑制剂在突触外膜蛋白和突触粘附蛋白的蛋白水解中的作用,以及蛋白水解对突触修饰和认知功能的影响。
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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来源期刊
Neuron glia biology
Neuron glia biology 医学-神经科学
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