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肌动蛋白在树突棘中的作用:连接动力学与功能。

Actin in dendritic spines: connecting dynamics to function.

机构信息

Neuroscience Center, University of Helsinki, 00014 Helsinki, Finland.

出版信息

J Cell Biol. 2010 May 17;189(4):619-29. doi: 10.1083/jcb.201003008. Epub 2010 May 10.

Abstract

Dendritic spines are small actin-rich protrusions from neuronal dendrites that form the postsynaptic part of most excitatory synapses and are major sites of information processing and storage in the brain. Changes in the shape and size of dendritic spines are correlated with the strength of excitatory synaptic connections and heavily depend on remodeling of its underlying actin cytoskeleton. Emerging evidence suggests that most signaling pathways linking synaptic activity to spine morphology influence local actin dynamics. Therefore, specific mechanisms of actin regulation are integral to the formation, maturation, and plasticity of dendritic spines and to learning and memory.

摘要

树突棘是神经元树突上富含肌动蛋白的小突起,构成了大多数兴奋性突触的突触后部分,也是大脑中信息处理和存储的主要部位。树突棘的形状和大小的变化与兴奋性突触连接的强度相关,并严重依赖于其下的肌动蛋白细胞骨架的重塑。新出现的证据表明,将突触活动与棘形态联系起来的大多数信号通路都影响局部肌动蛋白动力学。因此,肌动蛋白调节的特定机制是树突棘形成、成熟和可塑性以及学习和记忆的重要组成部分。

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