Center for Neuroscience and Department of Neurology of Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Elife. 2020 May 18;9:e55342. doi: 10.7554/eLife.55342.
Methyl-CpG-binding protein 2 (MeCP2) encoded by the gene is a transcriptional regulator whose mutations cause Rett syndrome (RTT). -deficient mice show fear regulation impairment; however, the cellular and molecular mechanisms underlying this abnormal behavior are largely uncharacterized. Here, we showed that gene deficiency in cholinergic interneurons of the nucleus accumbens (NAc) dramatically impaired fear learning. We further found that spontaneous activity of cholinergic interneurons in -deficient mice decreased, mediated by enhanced inhibitory transmission via α2-containing GABA receptors. With MeCP2 restoration, opto- and chemo-genetic activation, and RNA interference in ChAT-expressing interneurons of the NAc, impaired fear retrieval was rescued. Taken together, these results reveal a previously unknown role of MeCP2 in NAc cholinergic interneurons in fear regulation, suggesting that modulation of neurons in the NAc may ameliorate fear-related disorders.
甲基化 CpG 结合蛋白 2(MeCP2)由 基因编码,是一种转录调节因子,其突变导致雷特综合征(RTT)。 -缺陷小鼠表现出恐惧调节损伤;然而,这种异常行为的细胞和分子机制在很大程度上尚未阐明。在这里,我们表明, 基因在伏隔核(NAc)胆碱能中间神经元中的缺失极大地损害了恐惧学习。我们进一步发现, -缺陷小鼠中胆碱能中间神经元的自发活动减少,这是通过增强含有 α2 的 GABA 受体的抑制性传递介导的。通过 MeCP2 的恢复、光遗传和化学遗传激活以及 NAc 中 ChAT 表达中间神经元的 RNA 干扰,受损的恐惧检索得到了挽救。总之,这些结果揭示了 MeCP2 在 NAc 胆碱能中间神经元中对恐惧调节的未知作用,表明调节 NAc 中的神经元可能改善与恐惧相关的障碍。