Small G Protein Signaling in Neuronal Plasticity and Memory Formation: The Specific Role of Ras Family Proteins

被引:114
作者
Ye, Xiaojing [1 ]
Carew, Thomas J. [1 ]
机构
[1] Univ Calif Irvine, Ctr Neurobiol Learning & Memory, Dept Neurobiol & Behav, Irvine, CA 92697 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
LONG-TERM POTENTIATION; PHOSPHOINOSITIDE 3-KINASE-AKT-MAMMALIAN TARGET; NEUROFIBROMATOSIS TYPE-1 GENE; GTPASE-ACTIVATING PROTEIN; AMPA RECEPTOR TRAFFICKING; APLYSIA SENSORY NEURONS; NERVE GROWTH-FACTOR; SYNAPTIC PLASTICITY; MAP KINASE; DENDRITIC SPINE;
D O I
10.1016/j.neuron.2010.09.013
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Small G proteins are an extensive family of proteins that bind and hydrolyze GTP. They are ubiquitous inside cells, regulating a wide range of cellular processes. Recently, many studies have examined the role of small G proteins, particularly the Ras family of G proteins, in memory formation. Once thought to be primarily involved in the transduction of a variety of extracellular signals during development, it is now clear that Ras family proteins also play critical roles in molecular processing underlying neuronal and behavioral plasticity. We here review a number of recent studies that explore how the signaling of Ras family proteins contributes to memory formation. Understanding these signaling processes is of fundamental importance both from a basic scientific perspective, with the goal of providing mechanistic insights into a critical aspect of cognitive behavior, and from a clinical perspective, with the goal of providing effective therapies for a range of disorders involving cognitive impairments.
引用
收藏
页码:340 / 361
页数:22
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