MicroRNA-Mediated Rescue of Fear Extinction Memory by miR-144-3p in Extinction-Impaired Mice

被引:40
作者
Murphy, Conor P. [1 ]
Li, Xiang [3 ]
Maurer, Verena [1 ]
Oberhauser, Michael [1 ]
Gstir, Ronald [2 ]
Wearick-Silva, Luis Eduardo [4 ]
Viola, Thiago Wendt [4 ]
Schafferer, Simon [2 ]
Grassi-Oliveira, Rodrigo [4 ]
Whittle, Nigel [1 ,5 ]
Huttenhofer, Alexander [2 ]
Bredy, Timothy W. [3 ,6 ]
Singewald, Nicolas [1 ]
机构
[1] Univ Innsbruck, Ctr Mol Biosci Innsbruck, Inst Pharm, Dept Pharmacol & Toxicol, Innsbruck, Austria
[2] Innsbruck Med Univ, Bioctr Innsbruck, Div Genom & RNom, Innsbruck, Austria
[3] Univ Calif Irvine, Dept Neurobiol & Behav, Irvine, CA USA
[4] Pontifical Catholic Univ Rio Grande do Sul PUCRS, Dev Cognit Neurosci Res Grp GNCD, Porto Alegre, RS, Brazil
[5] Friedrich Miescher Inst Biomed Res, Basel, Switzerland
[6] Univ Queensland, Queensland Brain Inst, Brisbane, Qld, Australia
基金
英国医学研究理事会; 奥地利科学基金会;
关键词
Anxiety- and trauma-related disorders; Basolateral amygdala; Fear; MicroRNAs; PI3K/AKT; Signaling cascade modulation; GENETIC MOUSE MODEL; DOWN-REGULATION; CELL-PROLIFERATION; SIGNALING PATHWAY; CONDITIONED FEAR; CONTEXTUAL FEAR; AMYGDALA; EXPRESSION; ACTIVATION; PLASTICITY;
D O I
10.1016/j.biopsych.2016.12.021
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
BACKGROUND: MicroRNA (miRNA)-mediated control of gene expression suggests that miRNAs are interesting targets and/or biomarkers in the treatment of anxiety-and trauma-related disorders, where often memory-associated gene expression is adversely affected. METHODS: The role of miRNAs in the rescue of impaired fear extinction was assessed using the 129S1/SvlmJ (S1) mouse model of impaired fear extinction. miRNA microarray analysis, reverse transcription polymerase chain reaction, fluorescent in situ hybridization, lentiviral overexpression, and Luciferase reporter assays were used to gain insight into the mechanisms underlying miRNA-mediated normalization of deficient fear extinction. RESULTS: Rescuing impaired fear extinction via dietary zinc restriction was associated with differential expression of miRNAs in the amygdala. One candidate, miR-144-3p, robustly expressed in the basolateral amygdala, showed specific extinction-induced, but not fear-induced, increased expression in both extinction-rescued S1 mice and extinction-intact C57BL/6 (BL6) mice. miR-144-3p upregulation and effects on subsequent behavioral adaption was assessed in S1 and BL6 mice. miR-144-3p overexpression in the basolateral amygdala rescued impaired fear extinction in S1 mice, led to enhanced fear extinction acquisition in BL6 mice, and furthermore protected against fear renewal in BL6 mice. miR-144-3p targets a number of genes implicated in the control of plasticity-associated signaling cascades, including Pten, Spred1, and Notch1. In functional interaction studies, we revealed that the miR-144-3p target, PTEN, colocalized with miR-144-3p in the basolateral amygdala and showed functional down-regulation following successful fear extinction in S1 mice. CONCLUSIONS: These findings identify a fundamental role of miR-144-3p in the rescue of impaired fear extinction and suggest this miRNA as a viable target in developing novel treatments for posttraumatic stress disorder and related disorders.
引用
收藏
页码:979 / 989
页数:11
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