Hong Suk Jin, Li Huiwu, Becker Kevin G, Dawson Valina L, Dawson Ted M
Department of Neurology, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Proc Natl Acad Sci U S A. 2004 Feb 17;101(7):2145-50. doi: 10.1073/pnas.0305170101. Epub 2004 Feb 6.
The excitatory neurotransmitter, glutamate, activates N-methyl-d-aspartate (NMDA) receptors to induce long-lasting synaptic changes through alterations in gene expression. It is believed that these long-lasting changes contribute to learning and memory, drug tolerance, and ischemic preconditioning. To identify NMDA-induced late-response genes, we used a powerful gene-identification method, differential analysis of primary cDNA library expression (DAzLE), and cDNA microarray from primary cortical neurons. We report here that a variety of genes, which we have named plasticity-induced genes (PLINGs), are up-regulated with differential expression patterns after NMDA receptor activation, indicating that there is a broad and dynamic range of long-lasting neuronal responses that occur through NMDA receptor activation. Our results provide a molecular dissection of the activity-dependent long-lasting neuronal responses induced by NMDA receptor activation.
兴奋性神经递质谷氨酸通过改变基因表达激活N-甲基-D-天冬氨酸(NMDA)受体,以诱导持久的突触变化。据信,这些持久变化有助于学习与记忆、药物耐受性及缺血预处理。为鉴定NMDA诱导的晚期反应基因,我们使用了一种强大的基因鉴定方法,即原代cDNA文库表达差异分析(DAzLE),以及来自原代皮质神经元的cDNA微阵列。我们在此报告,多种基因(我们将其命名为可塑性诱导基因,即PLINGs)在NMDA受体激活后以差异表达模式上调,这表明通过NMDA受体激活会发生广泛且动态的持久神经元反应。我们的结果对NMDA受体激活诱导的活性依赖性持久神经元反应进行了分子剖析。