Department of Psychology, Yale University, New Haven, Connecticut 06520, USA.
J Neurochem. 2010 Feb;112(3):636-50. doi: 10.1111/j.1471-4159.2009.06491.x. Epub 2009 Nov 12.
Most recent studies aimed at defining the cellular and molecular mechanisms of Pavlovian fear conditioning have focused on protein kinase signaling pathways and the transcription factor cAMP-response element binding protein (CREB) that promote fear memory consolidation in the lateral nucleus of the amygdala (LA). Despite this progress, there still remains a paucity of information regarding the genes downstream of CREB that are required for long-term fear memory formation in the LA. We have adopted a strategy of using microarray technology to initially identify genes induced within the dentate gyrus following in vivo long-term potentiation (LTP) followed by analysis of whether these same genes are also regulated by fear conditioning within the LA. In the present study, we first identified 34 plasticity-associated genes that are induced within 30 min following LTP induction utilizing a combination of DNA microarray, qRT-PCR, and in situ hybridization. To determine whether these genes are also induced in the LA following Pavlovian fear conditioning, we next exposed rats to an auditory fear conditioning protocol or to control conditions that do not support fear learning followed by qRT-PCR on mRNA from microdissected LA samples. Finally, we asked whether identified genes induced by fear learning in the LA are downstream of the extracellular-regulated kinase/mitogen-activated protein kinase signaling cascade. Collectively, our findings reveal a comprehensive list of genes that represent the first wave of transcription following both LTP induction and fear conditioning that largely belong to a class of genes referred to as 'neuronal activity dependent genes' that are likely calcium, extracellular-regulated kinase/mitogen-activated protein kinase, and CREB-dependent.
最近的研究旨在定义巴甫洛夫式恐惧条件反射的细胞和分子机制,主要集中在蛋白激酶信号通路和转录因子 cAMP 反应元件结合蛋白(CREB)上,这些蛋白促进了杏仁核外侧核(LA)中的恐惧记忆巩固。尽管取得了这些进展,但对于 CREB 下游的基因,仍缺乏有关其在 LA 中长期恐惧记忆形成所必需的信息。我们采用了一种策略,即使用微阵列技术来初步鉴定体内长时程增强(LTP)后齿状回中诱导的基因,然后分析这些基因是否也受 LA 内的恐惧条件作用调节。在本研究中,我们首先利用 DNA 微阵列、qRT-PCR 和原位杂交技术,确定了 34 个在 LTP 诱导后 30 分钟内诱导的可塑性相关基因。为了确定这些基因是否也在 LA 中因巴甫洛夫式恐惧条件作用而被诱导,我们接下来使大鼠暴露于听觉恐惧条件作用方案或不支持恐惧学习的对照条件下,然后对微切割的 LA 样本中的 mRNA 进行 qRT-PCR。最后,我们询问了在 LA 中因恐惧学习而被诱导的基因是否是细胞外调节激酶/丝裂原活化蛋白激酶信号级联的下游。总的来说,我们的研究结果揭示了一组广泛属于所谓的“神经元活性依赖基因”的基因,这些基因代表了 LTP 诱导和恐惧条件作用后转录的第一波,它们可能是钙、细胞外调节激酶/丝裂原活化蛋白激酶和 CREB 依赖性的。