Roles for Arc in metabotropic glutamate receptor-dependent LTD and synapse elimination: Implications in health and disease

被引:39
|
作者
Wilkerson, Julia R. [1 ]
Albanesi, Joseph P. [2 ]
Huber, Kimberly M. [1 ]
机构
[1] Univ Texas Southwestern Med Ctr Dallas, Dept Neurosci, Dallas, TX 75390 USA
[2] Univ Texas Southwestern Med Ctr Dallas, Dept Pharmacol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
Arc/Arg3.1; Dynamin; mGluR5; Long-term synaptic depression; Synapse elimination; LONG-TERM DEPRESSION; MENTAL-RETARDATION PROTEIN; FRAGILE-X-SYNDROME; IMMEDIATE-EARLY GENE; MOUSE MODEL; MESSENGER-RNA; ALLOSTERIC MODULATION; ANGELMAN SYNDROME; CRYSTAL-STRUCTURE; GTPASE ACTIVITY;
D O I
10.1016/j.semcdb.2017.09.035
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Arc gene is robustly transcribed in specific neural ensembles in response to experience-driven activity. Upon induction, Arc mRNA is transported to dendrites, where it can be rapidly and locally translated by activation of metabotropic glutamate receptors (mGluR1/5). mGluR-induced dendritic synthesis of Arc is implicated in weakening or elimination of excitatory synapses by triggering endocytosis of postsynaptic AMPARs in both hippocampal CA1 and cerebellar Purkinje neurons. Importantly, CA1 neurons with experience-induced Arc mRNA are susceptible, or primed for mGluR-induced long-term synaptic depression (mGluR-LTD). Here we review mechanisms and function of Arc in mGluR-LTD and synapse elimination and propose roles for these forms of plasticity in Arc-dependent formation of sparse neural representations of learned experience. We also discuss accumulating evidence linking dysregulation of Arc and mGluR-LTD in human cognitive disorders such as intellectual disability, autism and Alzheimer's disease. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:51 / 62
页数:12
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