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Modified Glutamatergic Postsynapse in Neurodegenerative Disorders

机译:神经退行性疾病的改性谷氨酸后期后期

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摘要

postsynaptic density (PSD) is a complex subcellular domain important for postsynaptic signaling, function, and plasticity. The PSD is present at excitatory synapses and specialized to allow for precise neuron-toneuron transmission of information. The PSD is localized immediately underneath the postsynaptic membrane forming a major protein network that regulates postsynaptic signaling and synaptic plasticity. Glutamatergic synaptic dysfunction affecting PSD morphology and signaling events have been described in many neurodegenerative disorders, either sporadic or familial forms. Thus, in this review we describe the main protein players form ing the PSD and their activity, as well as relevant modifications in key components of the postsynaptic architecture occurring in Huntington's, Parkinson's and Alzheimer's diseases. This article is part of a Special Issue entitled: Lifestyle and Brain Metaplasticity. (c) 2019 IBRO. Published by Elsevier Ltd. All rights reserved.
机译:突触后密度(PSD)是一个复杂的亚细胞结构域,对突触后信号传导、功能和可塑性具有重要意义。PSD存在于兴奋性突触中,专门用于精确的神经元-神经元信息传递。PSD位于突触后膜的正下方,形成一个调节突触后信号和突触可塑性的主要蛋白质网络。影响PSD形态和信号事件的谷氨酸能突触功能障碍已在许多神经退行性疾病中被描述,无论是散发性还是家族性。因此,在这篇综述中,我们描述了形成PSD的主要蛋白质及其活性,以及亨廷顿氏症、帕金森氏症和阿尔茨海默氏症中突触后结构关键成分的相关修饰。这篇文章是特刊《生活方式和大脑可塑性》的一部分。(c) 2019年伊布罗。爱思唯尔有限公司出版。版权所有。

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