Molecular mechanisms of homeostatic synaptic downscaling

NEUROPHARMACOLOGY

卷:78

Review

Siddoway, Benjamin¹  Hou, Hailong¹  Xia, Houhui¹ 

[1] Louisiana State Univ, Hlth Sci Ctr, Neurosci Ctr Excellence, New Orleans, LA 70112 USA

关键词: Synapse;    Synaptic scaling;    Synaptic depression;    Immediate early genes;    Proteasome degradation;    Phosphorylation;   

DOI  :  10.1016/j.neuropharm.2013.07.009

来源: Elsevier

【 摘 要 】

Homeostatic synaptic downscaling is a negative feedback response to chronic elevated network activity to reduce the firing rate of neurons. This form of synaptic plasticity decreases the strength of individual synapses to the same proportion, or in a multiplicative manner. Because of this, synaptic downscaling has been hypothesized to counter the potential run-away excitation due to Hebbian type of long term potentiation (LTP), while preserving relative synaptic weight encoded in individual synapses and thus memory information. In this article, we will review the current knowledge on the signaling and molecular mechanisms of synaptic downscaling. Specifically, we focus on three general areas. First the functional roles of several immediate early genes such as PlK2, Homerl a, Arc and Narp are discussed. Secondly, we examine the current knowledge on the regulation of synaptic protein levels by ubiquitination and transcriptional repression in synaptic downscaling. Thirdly, we review the dynamics of signaling molecules such as kinases and phosphatases critical for synaptic downscaling, and their regulation of synaptic scaffolding proteins. Finally we briefly discuss the heterogeneity of homeostatic synaptic downscaling mechanisms. This article is part of the Special Issue entitled 'Homeostatic Synaptic Plasticity'. (C) 2013 Elsevier Ltd. All rights reserved.

【 授权许可】

Free