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健康与疾病状态下海马代谢型谷氨酸受体的长时程抑制:聚焦于丝裂原活化蛋白激酶通路

Hippocampal metabotropic glutamate receptor long-term depression in health and disease: focus on mitogen-activated protein kinase pathways.

作者信息

Sanderson Thomas M, Hogg Ellen L, Collingridge Graham L, Corrêa Sonia A L

机构信息

Centre for Synaptic Plasticity, School of Physiology, Pharmacology & Neuroscience, University of Bristol, Bristol, UK.

Bradford School of Pharmacy, Faculty of Life Sciences, University of Bradford, Bradford, UK.

出版信息

J Neurochem. 2016 Oct;139 Suppl 2:200-214. doi: 10.1111/jnc.13592. Epub 2016 May 4.

Abstract

Group I metabotropic glutamate receptor (mGluR) dependent long-term depression (LTD) is a major form of synaptic plasticity underlying learning and memory. The molecular mechanisms involved in mGluR-LTD have been investigated intensively for the last two decades. In this 60th anniversary special issue article, we review the recent advances in determining the mechanisms that regulate the induction, transduction and expression of mGluR-LTD in the hippocampus, with a focus on the mitogen-activated protein kinase (MAPK) pathways. In particular we discuss the requirement of p38 MAPK and extracellular signal-regulated kinase 1/2 (ERK 1/2) activation. The recent advances in understanding the signaling cascades regulating mGluR-LTD are then related to the cognitive impairments observed in neurological disorders, such as fragile X syndrome and Alzheimer's disease. mGluR-LTD is a form of synaptic plasticity that impacts on memory formation. In the hippocampus mitogen-activated protein kinases (MAPKs) have been found to be important in mGluR-LTD. In this 60th anniversary special issue article, we review the independent and complementary roles of two classes of MAPK, p38 and ERK1/2 and link this to the aberrant mGluR-LTD that has an important role in diseases. This article is part of the 60th Anniversary special issue.

摘要

I 型代谢型谷氨酸受体(mGluR)依赖的长时程抑制(LTD)是学习和记忆背后突触可塑性的主要形式。在过去二十年中,人们对参与 mGluR-LTD 的分子机制进行了深入研究。在这篇 60 周年特刊文章中,我们回顾了在确定调节海马体中 mGluR-LTD 的诱导、转导和表达机制方面的最新进展,重点关注丝裂原活化蛋白激酶(MAPK)途径。特别是,我们讨论了 p38 MAPK 和细胞外信号调节激酶 1/2(ERK 1/2)激活的必要性。然后,将理解调节 mGluR-LTD 的信号级联反应的最新进展与在神经疾病(如脆性 X 综合征和阿尔茨海默病)中观察到的认知障碍联系起来。mGluR-LTD 是一种影响记忆形成的突触可塑性形式。在海马体中,已发现丝裂原活化蛋白激酶(MAPKs)在 mGluR-LTD 中很重要。在这篇 60 周年特刊文章中,我们回顾了两类 MAPK,即 p38 和 ERK1/2 的独立和互补作用,并将其与在疾病中起重要作用的异常 mGluR-LTD 联系起来。本文是 60 周年特刊的一部分。

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