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α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体调节可塑性相关即早基因Arc的转录。

AMPA receptors regulate transcription of the plasticity-related immediate-early gene Arc.

作者信息

Rao Vikram R, Pintchovski Sean A, Chin Jeannie, Peebles Carol L, Mitra Siddhartha, Finkbeiner Steven

机构信息

Gladstone Institute of Neurological Disease, University of California, San Francisco, California 94158, USA.

出版信息

Nat Neurosci. 2006 Jul;9(7):887-95. doi: 10.1038/nn1708. Epub 2006 May 28.

Abstract

Learning and memory depend critically on long-term synaptic plasticity, which requires neuronal gene expression. In the prevailing view, AMPA receptors mediate fast excitatory synaptic transmission and effect short-term plasticity, but they do not directly regulate neuronal gene expression. By studying regulation of Arc, a gene required for long-term plasticity, we uncovered a new role for AMPA receptors in neuronal gene expression. Spontaneous synaptic activity or activity induced by brain-derived neurotrophic factor (BDNF) elicited Arc expression in cultures of rat cortical neurons and in organotypic brain slices. Notably, inhibiting AMPA receptors strongly potentiated activity-dependent Arc expression. We found that AMPA receptors negatively regulate Arc transcription, but not translation or stability, through a mechanism involving a pertussis toxin-sensitive G protein. These results provide insights into the activity-dependent mechanisms of Arc expression and suggest that, in addition to effecting short-term plasticity, AMPA receptors regulate genes involved in long-term plasticity.

摘要

学习和记忆严重依赖于长期突触可塑性,而这需要神经元基因表达。在普遍观点中,AMPA受体介导快速兴奋性突触传递并影响短期可塑性,但它们并不直接调节神经元基因表达。通过研究Arc(长期可塑性所需的一种基因)的调控,我们发现了AMPA受体在神经元基因表达中的新作用。自发突触活动或脑源性神经营养因子(BDNF)诱导的活动在大鼠皮质神经元培养物和脑片培养物中引发了Arc表达。值得注意的是,抑制AMPA受体会强烈增强活动依赖性Arc表达。我们发现,AMPA受体通过一种涉及百日咳毒素敏感G蛋白的机制对Arc转录进行负调控,但对翻译或稳定性没有影响。这些结果为Arc表达的活动依赖性机制提供了见解,并表明,除了影响短期可塑性外,AMPA受体还调节参与长期可塑性的基因。

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