Cited by 116MicroRNA in disease regulationNeuroscience and Neuropharmacology ResearchMemory and Neural Mechanisms

The DOI matches its Crossref record; 67 of the 67 references it cites were found in a registry or an index; 16 of the 31 sources its claims cite were checked for support.

The Brain-Enriched MicroRNA miR-9-3p Regulates Synaptic Plasticity and Memory

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Abstract

UNLABELLED: MicroRNAs (miRNAs) are small, noncoding RNAs that posttranscriptionally regulate gene expression in many tissues. Although a number of brain-enriched miRNAs have been identified, only a few specific miRNAs have been revealed as critical regulators of synaptic plasticity, learning, and memory. miR-9-5p/3p are brain-enriched miRNAs known to regulate development and their changes have been implicated in several neurological disorders, yet their role in mature neurons in mice is largely unknown. Here, we report that inhibition of miR-9-3p, but not miR-9-5p, impaired hippocampal long-term potentiation (LTP) without affecting basal synaptic transmission. Moreover, inhibition of miR-9-3p in the hippocampus resulted in learning and memory deficits. Furthermore, miR-9-3p inhibition increased the expression of the LTP-related genes Dmd and SAP97, the expression levels of which are negatively correlated with LTP. These results suggest that miR-9-3p-mediated gene regulation plays important roles in synaptic plasticity and hippocampus-dependent memory. SIGNIFICANCE STATEMENT: Despite the abundant expression of the brain-specific microRNA miR-9-5p/3p in both proliferating and postmitotic neurons, most functional studies have focused on their role in neuronal development. Here, we examined the role of miR-9-5p/3p in adult brain and found that miR-9-3p, but not miR-9-5p, has a critical role in hippocampal synaptic plasticity and memory. Moreover, we identified in vivo binding targets of miR-9-3p that are involved in the regulation of long-term potentiation. Our study provides the very first evidence for the critical role of miR-9-3p in synaptic plasticity and memory in the adult mouse.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

Inhibition of the brain-enriched microRNA miR-9-3p, but not miR-9-5p, impairs hippocampal long-term potentiation (LTP) and hippocampus-dependent memory in mice. miR-9-3p acts at least partly by suppressing LTP-related genes Dmd and SAP97, whose increased expression correlates with impaired LTP.

Key findings

  • miR-9-3p inhibition reduced theta-burst LTP at SC-CA1 synapses (last 5 min EPSC amplitude: control n=6 cells/3 mice; miR-9-3p n=9 cells/6 mice; naive n=7 cells/5 mice; one-way ANOVA F(2,19)=9.514, p=0.0014; Tukey control vs miR-9-3p and miR-9-3p vs naive, p<0.01), whereas miR-9-5p inhibition did not affect LTP (control n=12 cells/7 mice; miR-9-5p n=14 cells/6 mice; t(24)=0.8454, p=0.4062).
  • miR-9-3p inhibition did not significantly affect LTD (t(14)=0.6813, p=0.5068), basal synaptic transmission, membrane excitability, sEPSCs/sIPSCs/mEPSCs/mIPSCs, or NMDA receptor-mediated EPSCs.
  • miR-9-3p sponge-expressing mice showed impaired hippocampus-dependent memory: Morris water maze probe test (sponge × quadrant F(3,68)=4.44, p=0.0066; target quadrant control vs miR-9-3p p<0.05), object location memory (control t(7)=4.069, p=0.0048; miR-9-3p t(8)=0.9769, p=0.3572), and trace fear conditioning (last 4 test sessions t(6)=2.998, p=0.0241), without altered anxiety or locomotor activity.
  • miR-9-3p inhibition increased hippocampal protein levels of Dmd (control 100.0±14.0%, n=7 hippocampi; miR-9-3p 156.2±14.9%, n=8; t(13)=2.724, p=0.0173) and SAP97 (control 100.0±1.2%, n=5; miR-9-3p 125.2±7.8%, n=4; t(7)=3.606, p=0.0087), while miR-9-5p inhibition did not alter either.

Methods

  • Male C57BL/6N mice were used; AAV vectors expressing EGFP-tagged miR-9-3p, miR-9-5p, or control sponges under the human synapsin promoter were stereotaxically injected into dorsal CA1.
  • Electrophysiology used whole-cell patch-clamp recordings in acute hippocampal slices from 4- to 5-week-old mice; behavior used 8-week-old mice in Morris water maze, object location memory, trace fear conditioning, open-field, and elevated zero maze tasks.
  • Molecular validation combined TargetScan/Ingenuity Pathway Analysis target prediction, luciferase reporter assays with wild-type or mutated 3′ UTRs, and Western blots from CA1 regions expressing EGFP.

Limitations

  • The paper states that LTP was induced by theta-burst stimulation with relatively short intervals, which may not be sensitive to protein synthesis and PKA inhibitors; whether miR-9-3p also regulates the protein-synthesis-dependent form of LTP remains to be determined.
  • The paper notes that SAP97 was increased by miR-9-3p inhibition but no changes in excitatory synaptic transmission were detected, consistent with prior work in mature neurons.
  • Evident from the text: all experiments used male mice, so sex differences are not addressed; in vivo target validation focused on Dmd and SAP97 among seven candidate genes, leaving the other candidates unvalidated in vivo.

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Integrity signals

Registry

Crossref · 10.1523/jneurosci.0630-16.2016

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Metadata

Authors
Sim, S.-E., Lim, C.-S., Kim, J.-I., Seo, D., Chun, H., Yu, N.-K., Lee, J., Kang, S. J., Ko, H.-G., Choi, J.-H., Kim, T., Jang, E.-H., Han, J., Bak, M. S., Park, J.-E., Jang, D.-J., Baek, D., Lee, Y.-S., & Kaang, B.-K.
Affiliations
  • Department of Biological Sciences (RU)
  • Institute for Basic Science (KR)
  • Chung-Ang University (KR)
  • Kyungpook National University (KR)
  • Seoul National University (KR)
Venue
The Journal of Neuroscience
Published
2016-08-17
Volume
36
Issue
33
Pages
8641-8652
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W2510924509
Cited by
116
References
67
Citations by year
2026: 4 · 2025: 12 · 2024: 18 · 2023: 11 · 2022: 16 · 2021: 10 · 2020: 15 · 2019: 15 · 2018: 8 · 2017: 7
FWCI
3.57
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Seoul National University Open Repository (Seoul National University) (submittedVersion)
  • Scholarworks@UNIST (Ulsan National Institute of Science and Technology) (submittedVersion)
Funders
  • National Research Foundation
  • National Research Foundation of Korea (2012R1A3A1050385)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Keywords
miR-9-3p, miR-9-5p, microRNA, synaptic plasticity, long-term potentiation, hippocampus, learning and memory, DMD, SAP97, post-transcriptional regulation, adult neurons, miRNA target genes
MeSH terms
Discs Large Homolog 1 Protein, Animals, Conditioning, Psychological, Exploratory Behavior, Fear, Hippocampus, Humans, Male, Membrane Proteins, Mice, Inbred C57BL, Neuronal Plasticity, Transduction, Genetic, Dystrophin, Synapsins, Maze Learning, Receptors, CXCR4, Recognition, Psychology, MicroRNAs, Green Fluorescent Proteins, Mice, Guanylate Kinases, HEK293 Cells

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