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miR-181a 通过靶向 PRKAA1 参与海马依赖性记忆形成。

miR-181a involves in the hippocampus-dependent memory formation via targeting PRKAA1.

机构信息

Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, Sichuan, P. R. China.

Department of Neurosurgery, The First People's Hospital of Yibin, Yibin, Sichuan, P. R. China.

出版信息

Sci Rep. 2017 Aug 16;7(1):8480. doi: 10.1038/s41598-017-09095-3.

DOI:10.1038/s41598-017-09095-3
PMID:28814760
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5559581/
Abstract

Post-transcriptional gene regulation by microRNAs (miRNAs) is involved in memory formation. However, the roles of individual miRNAs in these processes remain largely unknown. In this study, we want to clarify the role of miR-181a in hippocampus-dependent memory formation. A transient increase in miR-181a expression was observed after conditioned fear conditioning (CFC) and object location task (OLT) training. Selective overexpression or inhibition of miR-181a in the dorsal hippocampus (DH) via the injection of a miR-181a agomir or antagomir enhanced or impaired the CFC- and OLT-dependent memory formation, respectively. Using bioinformatics and luciferase assays, we identified PRKAA1 as a potential target gene of miR-181a. After CFC or OLT training, the expression and activity of PRKAA1 decreased as miR-181a expression increased and was effectively blocked by the miR-181a antagomir. Moreover, microinjection of the PRKAA1 agonist AICAR or inhibitor compound C in the DH reversed the roles of the miR-181a agomir or antagomir in CFC- and OLT-dependent memory formation. In conclusion, this work provides novel evidence describing the role and mechanism of miR-181a in hippocampus-dependent memory formation, which sheds light on the potential regulation of cognition and future treatments for cognitive disorders.

摘要

miRNAs(微小 RNA)对基因的转录后调控参与了记忆的形成。然而,个别 miRNAs 在这些过程中的作用在很大程度上仍是未知的。在本研究中,我们旨在阐明 miR-181a 在海马体依赖性记忆形成中的作用。在条件性恐惧条件反射(CFC)和物体位置任务(OLT)训练后,观察到 miR-181a 的表达短暂增加。通过注射 miR-181a 激动剂或拮抗剂,在背侧海马体(DH)中选择性地上调或下调 miR-181a 的表达,分别增强或损害了 CFC 和 OLT 依赖性记忆的形成。通过生物信息学和荧光素酶测定,我们鉴定出 PRKAA1 是 miR-181a 的一个潜在靶基因。在 CFC 或 OLT 训练后,随着 miR-181a 表达的增加,PRKAA1 的表达和活性下降,并且这种下降可被 miR-181a 拮抗剂有效阻断。此外,在 DH 中注射 PRKAA1 激动剂 AICAR 或抑制剂化合物 C 可逆转 miR-181a 激动剂或拮抗剂在 CFC 和 OLT 依赖性记忆形成中的作用。总之,这项工作提供了新的证据,描述了 miR-181a 在海马体依赖性记忆形成中的作用和机制,这为认知调节和未来认知障碍的治疗提供了新的思路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/8d92ec099f05/41598_2017_9095_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/451b34cbc393/41598_2017_9095_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/f9f3e161c279/41598_2017_9095_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/ad77380c2626/41598_2017_9095_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/ae5a3ffaad9e/41598_2017_9095_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/c7e6f5a942e0/41598_2017_9095_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/8d92ec099f05/41598_2017_9095_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/451b34cbc393/41598_2017_9095_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/f9f3e161c279/41598_2017_9095_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/ad77380c2626/41598_2017_9095_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/ae5a3ffaad9e/41598_2017_9095_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/c7e6f5a942e0/41598_2017_9095_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f898/5559581/8d92ec099f05/41598_2017_9095_Fig6_HTML.jpg

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