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小脑可塑性中的突触信号传导。

Synaptic signalling in cerebellar plasticity.

作者信息

Evans Gareth J O

机构信息

Department of Biology (Area 3), University of York, Heslington, York, UK.

出版信息

Biol Cell. 2007 Jul;99(7):363-78. doi: 10.1042/BC20070010.

Abstract

A major goal of learning and memory research is to correlate the function of molecules with the behaviour of organisms. The beautiful laminar structure of the cerebellar cortex lends itself to the study of synaptic plasticity, because its clearly defined patterns of neurons and their synapses form circuits that have been implicated in simple motor behaviour paradigms. The best understood in terms of molecular mechanism is the parallel fibre-Purkinje cell synapse, where presynaptic long-term potentiation and postsynaptic long-term depression and potentiation finely tune cerebellar output. Our understanding of these forms of plasticity has mostly come from the electrophysiological and behavioural analysis of knockout mutant mice, but more recently the knock-in of synaptic molecules with mutated phosphorylation sites and binding domains has provided more detailed insights into the signalling events. The present review details the major forms of plasticity in the cerebellar cortex, with particular attention to the membrane trafficking and intracellular signalling responsible. This overview of the current literature suggests it will not be long before the involvement of the cerebellum in certain motor behaviours is fully explained in molecular terms.

摘要

学习与记忆研究的一个主要目标是将分子功能与生物体行为联系起来。小脑皮质优美的分层结构便于研究突触可塑性,因为其明确界定的神经元及其突触模式形成了与简单运动行为范式相关的回路。就分子机制而言,理解最透彻的是平行纤维 - 浦肯野细胞突触,在该突触中,突触前长时程增强以及突触后长时程抑制和增强对小脑输出进行精细调节。我们对这些可塑性形式的理解大多来自基因敲除突变小鼠的电生理和行为分析,但最近对具有突变磷酸化位点和结合结构域的突触分子进行基因敲入,为信号转导事件提供了更详细的见解。本综述详细介绍了小脑皮质可塑性的主要形式,特别关注负责的膜转运和细胞内信号转导。对当前文献的这一概述表明,用分子术语全面解释小脑在某些运动行为中的作用为时不远。

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