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p38丝裂原活化蛋白激酶及其底物在神经元可塑性和神经退行性疾病中的作用

The Role of p38 MAPK and Its Substrates in Neuronal Plasticity and Neurodegenerative Disease.

作者信息

Corrêa Sônia A L, Eales Katherine L

机构信息

School of Life Sciences, The University of Warwick, Coventry CV4 7AL, UK.

出版信息

J Signal Transduct. 2012;2012:649079. doi: 10.1155/2012/649079. Epub 2012 Jun 25.

Abstract

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.

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。在本综述中,我们将讨论p38 MAPK的细胞定位和激活,以及其底物MAPKAPK 2(MK2)和tau蛋白的分子和细胞机制的最新进展。特别是,我们将重点关注对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蛋白过度磷酸化方面的理解,这些过程被认为与正常衰老以及神经退行性疾病有关。我们还将深入探讨阐明p38 MAPK-MK2和p38 MAPK-tau信号级联的精确作用如何有助于识别新的治疗靶点,以减缓在阿尔茨海默病和帕金森病等神经退行性疾病中观察到的症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fb7b/3389708/c2e68ca0df2f/JST2012-649079.001.jpg

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