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CaMK和RacGEF信号汇聚控制树突结构与功能。

Convergent CaMK and RacGEF signals control dendritic structure and function.

作者信息

Penzes Peter, Cahill Michael E, Jones Kelly A, Srivastava Deepak P

机构信息

Department of Physiology, Northwestern University Feinberg School of Medicine, 303 E. Chicago Avenue, Chicago, IL 60611, USA.

出版信息

Trends Cell Biol. 2008 Sep;18(9):405-13. doi: 10.1016/j.tcb.2008.07.002. Epub 2008 Aug 11.

Abstract

Structural plasticity of excitatory synapses is a vital component of neuronal development, synaptic plasticity and behavior, and its malfunction underlies many neurodevelopmental and psychiatric disorders. However, the molecular mechanisms that control dendritic spine morphogenesis have only recently emerged. We summarize recent work that has revealed an important connection between calcium/calmodulin-dependent kinases (CaMKs) and guanine-nucleotide-exchange factors (GEFs) that activate the small GTPase Rac (RacGEFs) in controlling dendritic spine morphogenesis. These two groups of molecules function in neurons as a unique signaling cassette that transduces calcium influx into small GTPase activity and, thence, actin reorganization and spine morphogenesis. Through this pathway, CaMKs and RacGEFs amplify calcium signals and translate them into spatially and temporally regulated structural remodeling of dendritic spines.

摘要

兴奋性突触的结构可塑性是神经元发育、突触可塑性和行为的重要组成部分,其功能失调是许多神经发育和精神疾病的基础。然而,控制树突棘形态发生的分子机制直到最近才被发现。我们总结了最近的研究工作,这些研究揭示了钙/钙调蛋白依赖性激酶(CaMKs)和鸟嘌呤核苷酸交换因子(GEFs,即激活小GTP酶Rac的因子,RacGEFs)之间在控制树突棘形态发生方面的重要联系。这两组分子在神经元中作为一个独特的信号盒发挥作用,将钙内流转化为小GTP酶活性,进而导致肌动蛋白重组和树突棘形态发生。通过这条途径,CaMKs和RacGEFs放大钙信号,并将其转化为树突棘在空间和时间上受到调控的结构重塑。

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