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多巴胺能刺激局部蛋白质合成可增强海马神经元中GluR1的表面表达及突触传递。

Dopaminergic stimulation of local protein synthesis enhances surface expression of GluR1 and synaptic transmission in hippocampal neurons.

作者信息

Smith W Bryan, Starck Shelley R, Roberts Richard W, Schuman Erin M

机构信息

Division of Biology 114-96 and, HHMI, Pasadena, CA 91125, USA.

出版信息

Neuron. 2005 Mar 3;45(5):765-79. doi: 10.1016/j.neuron.2005.01.015.

Abstract

The use-dependent modification of synapses is strongly influenced by dopamine, a transmitter that participates in both the physiology and pathophysiology of animal behavior. In the hippocampus, dopaminergic signaling is thought to play a key role in protein synthesis-dependent forms of synaptic plasticity. The molecular mechanisms by which dopamine influences synaptic function, however, are not well understood. Using a GFP-based reporter, as well as a small-molecule reporter of endogenous protein synthesis, we show that dopamine D1/D5 receptor activation stimulates local protein synthesis in the dendrites of hippocampal neurons. We also identify the GluR1 subunit of AMPA receptors as one protein upregulated by dopamine receptor activation, with increased incorporation of surface GluR1 at synaptic sites. The insertion of new GluRs is accompanied by an increase in the frequency of miniature synaptic events. Together, these data suggest a local protein synthesis-dependent activation of previously silent synapses as a result of dopamine receptor stimulation.

摘要

突触的使用依赖性修饰受到多巴胺的强烈影响,多巴胺是一种参与动物行为生理和病理生理过程的神经递质。在海马体中,多巴胺能信号传导被认为在依赖蛋白质合成的突触可塑性形式中起关键作用。然而,多巴胺影响突触功能的分子机制尚不清楚。我们使用基于绿色荧光蛋白(GFP)的报告基因以及内源性蛋白质合成的小分子报告基因,证明多巴胺D1/D5受体激活可刺激海马神经元树突中的局部蛋白质合成。我们还确定AMPA受体的GluR1亚基是一种因多巴胺受体激活而上调的蛋白质,突触部位表面GluR1的掺入增加。新的谷氨酸受体插入伴随着微小突触事件频率的增加。这些数据共同表明,多巴胺受体刺激导致以前沉默的突触发生局部蛋白质合成依赖性激活。

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