p38 MAPK及其底物在神经元可塑性和神经退行性疾病中的作用。

Journal of signal transduction Pub Date : 2012-01-01 Epub Date: 2012-06-25 DOI:10.1155/2012/649079
Sônia A L Corrêa, Katherine L Eales
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引用次数: 206

摘要

大量证据表明p38-丝裂原活化蛋白激酶(MAPK)信号级联在突触可塑性和神经退行性疾病中起着至关重要的作用。在这篇综述中,我们将讨论p38 MAPK的细胞定位和激活及其底物MAPKAPK 2 (MK2)和tau蛋白的分子和细胞机制的最新进展。我们将特别关注p38 MAPK-MK2和p38 MAPK-tau激活轴在控制神经炎症、肌动蛋白重塑和tau过度磷酸化中的作用,这些过程被认为与正常衰老和神经退行性疾病有关。我们还将深入了解如何阐明p38 MAPK-MK2和p38 MAPK-tau信号级联的确切作用,可能有助于确定新的治疗靶点,以减缓神经退行性疾病(如阿尔茨海默病和帕金森病)中观察到的症状。
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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The Role of p38 MAPK and Its Substrates in Neuronal Plasticity and Neurodegenerative Disease.

A significant amount of evidence suggests that the p38-mitogen-activated protein kinase (MAPK) signalling cascade plays a crucial role in synaptic plasticity and in neurodegenerative diseases. In this review we will discuss the cellular localisation and activation of p38 MAPK and the recent advances on the molecular and cellular mechanisms of its substrates: MAPKAPK 2 (MK2) and tau protein. In particular we will focus our attention on the understanding of the p38 MAPK-MK2 and p38 MAPK-tau activation axis in controlling neuroinflammation, actin remodelling and tau hyperphosphorylation, processes that are thought to be involved in normal ageing as well as in neurodegenerative diseases. We will also give some insight into how elucidating the precise role of p38 MAPK-MK2 and p38 MAPK-tau signalling cascades may help to identify novel therapeutic targets to slow down the symptoms observed in neurodegenerative diseases such as Alzheimer's and Parkinson's disease.

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