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microRNA-34a 急性调控成年齿状回体内突触效能

MicroRNA-34a Acutely Regulates Synaptic Efficacy in the Adult Dentate Gyrus In Vivo.

机构信息

Department of Biomedicine, University of Bergen, Bergen, Norway.

KG Jebsen Centre for Neuropsychiatric Disorders, University of Bergen, Jonas Lies vei 91, 5009, Bergen, Norway.

出版信息

Mol Neurobiol. 2020 Mar;57(3):1432-1445. doi: 10.1007/s12035-019-01816-1. Epub 2019 Nov 21.

Abstract

Activity-dependent synaptic plasticity involves rapid regulation of neuronal protein synthesis on a time-scale of minutes. miRNA function in synaptic plasticity and memory formation has been elucidated by stable experimental manipulation of miRNA expression and activity using transgenic approaches and viral vectors. However, the impact of rapid miRNA modulation on synaptic efficacy is unknown. Here, we examined the effect of acute (12 min), intrahippocampal infusion of a miR-34a antagonist (antimiR) on medial perforant path-evoked synaptic transmission in the dentate gyrus of adult anesthetised rats. AntimiR-34a infusion acutely depressed medial perforant path-evoked field excitatory post-synaptic potentials (fEPSPs). The fEPSP decrease was detected within 9 min of infusion, lasted for hours, and was associated with knockdown of antimiR-34a levels. AntimiR-34a-induced synaptic depression was sequence-specific; no changes were elicited by infusion of scrambled or mismatch control. The rapid modulation suggests that a target, or set of targets, is regulated by miR-34a. Western blot analysis of dentate gyrus lysates revealed enhanced expression of Arc, a known miR-34a target, and four novel predicted targets (Ctip2, PKI-1α, TCF4 and Ube2g1). Remarkably, antimiR-34a had no effect when infused during the maintenance phase of long-term potentiation. We conclude that miR-34a regulates basal synaptic efficacy in the adult dentate gyrus in vivo. To our knowledge, these in vivo findings are the first to demonstrate acute (< 9 min) regulation of synaptic efficacy in the adult brain by a miRNA.

摘要

活动依赖性突触可塑性涉及神经元蛋白合成的快速调节,其时间尺度为分钟。通过使用转基因方法和病毒载体对 miRNA 表达和活性进行稳定的实验操作,miRNA 在突触可塑性和记忆形成中的功能已经得到阐明。然而,快速 miRNA 调节对突触效能的影响尚不清楚。在这里,我们研究了急性(12 分钟)海马内输注 miR-34a 拮抗剂(antimiR)对麻醉成年大鼠齿状回中内侧穿通路径诱发的突触传递的影响。antimiR-34a 输注急性抑制内侧穿通路径诱发的场兴奋性突触后电位(fEPSP)。输注后 9 分钟内即可检测到 fEPSP 下降,持续数小时,并与 antimiR-34a 水平的降低有关。antimiR-34a 诱导的突触抑制具有序列特异性;输注 scrambled 或错配对照不会引起变化。快速调节表明 miR-34a 调节一个或一组靶标。齿状回裂解物的 Western blot 分析显示,已知的 miR-34a 靶标 Arc 以及四个新预测的靶标(Ctip2、PKI-1α、TCF4 和 Ube2g1)的表达增强。值得注意的是,antimiR-34a 在长时程增强的维持阶段输注时没有效果。我们得出结论,miR-34a 在体内调节成年齿状回的基础突触效能。据我们所知,这些体内发现是首次证明 miRNA 在成年大脑中急性(<9 分钟)调节突触效能。

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