Department of Psychology, Yale University, New Haven, Connecticut 06520, USA.
Learn Mem. 2011 Aug 25;18(9):579-93. doi: 10.1101/lm.2243411. Print 2011 Sep.
Epigenetic mechanisms have been widely implicated in synaptic plasticity and in memory consolidation, yet little is known about the role of epigenetic mechanisms in memory reconsolidation processes. In the present study, we systematically examine the role of histone acetylation and DNA methylation in the reconsolidation of an amygdala-dependent Pavlovian fear memory. We first show that the acetylation of histone 3 (H3), but not histone 4 (H4), is regulated following auditory fear memory retrieval in the lateral nucleus of the amygdala (LA). We next show that histone deacetylase (HDAC) inhibition in the LA enhances both retrieval-induced histone acetylation and reconsolidation of an auditory fear memory. Conversely, inhibition of DNA methytransferase (DNMT) activity in the LA significantly impairs both retrieval-related H3 acetylation and fear memory reconsolidation. The effects of HDAC and DNMT inhibitors on fear memory reconsolidation were observed to be time-limited and were not evident in the absence of memory reactivation. Further, memories lost following DNMT inhibition were not observed to be vulnerable to spontaneous recovery, reinstatement, or to a shift in testing context, suggesting that memory impairment was not the result of facilitated extinction. Finally, pretreatment with the HDAC inhibitor was observed to rescue the reconsolidation deficit induced by the DNMT inhibitor. These findings collectively suggest that histone acetylation and DNA methylation are critical for reconsolidation of fear memories in the LA.
表观遗传机制广泛涉及突触可塑性和记忆巩固,但对于表观遗传机制在记忆再巩固过程中的作用知之甚少。在本研究中,我们系统地研究了组蛋白乙酰化和 DNA 甲基化在杏仁核依赖性条件性恐惧记忆再巩固中的作用。我们首先表明,在外侧杏仁核(LA)中听觉恐惧记忆检索后,组蛋白 3(H3)而非组蛋白 4(H4)的乙酰化受到调节。接下来我们发现,LA 中的组蛋白去乙酰化酶(HDAC)抑制增强了检索诱导的组蛋白乙酰化和听觉恐惧记忆的再巩固。相反,LA 中的 DNA 甲基转移酶(DNMT)活性抑制显著损害了与检索相关的 H3 乙酰化和恐惧记忆的再巩固。HDAC 和 DNMT 抑制剂对恐惧记忆再巩固的影响具有时间限制,如果没有记忆再激活,则不明显。此外,DNMT 抑制后丢失的记忆不会容易受到自发恢复、重新确立或测试情境转变的影响,这表明记忆损伤不是促进性消退的结果。最后,观察到 HDAC 抑制剂的预处理可挽救 DNMT 抑制剂诱导的再巩固缺陷。这些发现共同表明,组蛋白乙酰化和 DNA 甲基化对于 LA 中恐惧记忆的再巩固至关重要。